My main scientific interests concern experimental and clinical issues of chronic and acute myeloid neoplasms and molecular biology in Hematology diseases
347
Scopus Publications
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86
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264
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Scopus Publications
The Role and Impact of Non-driver Gene Mutations in Myelofibrosis Valentina Boldrini, Paola Guglielmelli, Alessandro M. Vannucchi Current Hematologic Malignancy Reports, 2026 Purpose of the Review Myelofibrosis (MF) is a myeloproliferative neoplasm (MPN) characterized by splenomegaly, constitutional symptoms, bone marrow fibrosis and potential progression to a blast phase. This review provides a comprehensive overview of the current molecular landscape of MF beyond canonical driver mutations ( JAK2 , MPL or CALR) , emphasizing insights gained from murine models that served as valuable tools for understanding disease mechanisms. Recent Findings High-throughput next-generation sequencing (NGS) has markedly enhanced our understanding of the molecular basis of MF, identifying numerous mutations beyond the canonical driver genes JAK2 , MPL , and CALR , which are present in about 80% of patients. Additional mutations affect genes involved in DNA methylation ( TET2 , DNMT3A , IDH1 , IDH2 ), histone modification ( ASXL1 , EZH2 ), mRNA splicing ( SF3B1 , SRSF2 , U2AF1 , ZRSR2 ), signaling pathways ( CBL , NRAS , KRAS ), and key transcription factors ( RUNX1 , NFE2 , TP53 ). The presence and combination of these alterations influence clinical presentation, prognosis, and therapeutic response. Summary This review offers an updated synthesis of the evolving molecular landscape of MF, highlighting how the intricate interplay among genetic alterations has deepened our understanding of disease heterogeneity, allowing refined risk stratification and therapeutic planning. Advances emerging from molecular research and experimental models are progressively translating into clinical practice, promoting more personalized and targeted approaches to the management of MF.
Genomic structural variations contribute to inform prognosis in patients with cytogenetically normal acute myeloid leukemia Niccolò Bartalucci, Francesco Mannelli, Danilo Tarantino, Alessio Enderti, Simone Romagnoli, Daniele Colazzo, Barbara Scappini, Giacomo Gianfaldoni, Matteo Piccini, Leonardo Signori, Fiorenza Irushani, Silvia Salmoiraghi, Tiziana Ottone, Alfonso Piciocchi, Margherita Vannucchi, Maria Chiara Siciliano, Roberto Boccacci, Silvia Orsi, Alessia Civini, Paola Fazi, Raffaella Santi, Marco Vignetti, Stefania Bortoluzzi, Alberto Bosi, Adriano Venditti, Alessandro Rambaldi, Maria Teresa Voso, Paola Guglielmelli, Alessandro M. Vannucchi Blood Cancer Journal, 2026 Cytogenetic and genomic profiling of acute myeloid leukemia (AML) guides personalized treatment according to ELN2022 recommendations. However, marked outcome variability persists among cytogenetically normal (CN-) patients, representing an unmet clinical need. We used long-read whole-genome sequencing to interrogate the prognostic significance of structural variations (SVs) in a prospective cohort of 162 intensively treated CN-AML patients. After stringent filtering, we identified 5 somatic SVs associated with shorter overall survival (OS) (HR:4.18, p < 0.001) and event-free survival (EFS) (HR:3.59, p < 0.001) in 13% of the patients. Results were validated in a real-world cohort of 149 CN-AML, using target assays. These high-risk SVs (HRVs) operationally defined a “very high-risk” category in the framework of ELN2022, overall resulting in more accurate OS prediction. HRVs were independent of most frequent mutations, particularly FLT3ITD and NPM1mut. Among the latter patients, HRVs independently predicted shorter OS (8.2 months versus not-reached; p < 0.001), EFS (3.5 versus 25.7 months; p < 0.001), and lower complete response rates (66.7% versus 90.1%; p < 0.005). Finally, we provided evidence of transcriptional deregulation of SV-related genes in primary samples and engineered cell models. Current findings support the value of SVs for refining risk stratification in CN-AML, by identifying patients at exceedingly dismal outcome who might benefit from personalized approaches.
Autoimmune and Inflammatory Diseases in Polycythemia Vera and Essential Thrombocythemia: Impact on Disease Outcomes and Comorbidities Giuseppe G. Loscocco, Fnu Aperna, Moazah Iftikhar, Priyansh Faldu, Masooma S. Rana, Animesh Pardanani, Paola Guglielmelli, Alessandro M. Vannucchi, Naseema Gangat, Ayalew Tefferi American Journal of Hematology, 2026 Polycythemia vera (PV) and essential thrombocythemia (ET) are chronic Philadelphia chromosome negative myeloproliferative neoplasms (MPN) characterized by clonal hematopoiesis, thrombotic risk, and variable disease evolution [1, 2]. Increasing evidence supports a role for immune dysregulation and inflammatory pathways in disease development and clinical heterogeneity, although their clinical implications remain incompletely defined [3]. Epidemiological studies have reported an association between prior autoimmune diseases and an increased risk of developing MPN [4]. Autoimmune or inflammatory diseases (AID) have also been described in approximately 6%–8% of patients with MPN, with heterogeneous effects on clinical features and survival across cohorts [5, 6]. However, the clinical burden of AID in patients specifically affected by PV and ET, particularly concerning disease outcomes and comorbidity profiles, remains poorly defined. We therefore evaluated the prevalence of AID in a large cohort of patients with PV and ET and assessed their association with disease outcomes and comorbidities. Institutional review board approval was obtained from the Mayo Clinic, Rochester, MN, USA, for retrospective data collection in accordance with the Declaration of Helsinki. The study included consecutive patients with PV and ET evaluated between 1970 and 2024 and diagnosed according to the 2022 International Consensus Classification criteria [7]. AID were defined according to established disease-specific clinical and serologic criteria. Clinical and laboratory variables were collected at diagnosis or first referral. Thrombotic events were confirmed by imaging studies and classified as arterial or venous; AID, cancers, and thrombotic events were categorized as occurring before/at or after MPN diagnosis using a ≥ 3 month interval. Overall survival was estimated using the Kaplan–Meier method and compared using the log-rank test. Competing-risk analyses were performed for thrombosis, leukemic transformation, myelofibrosis progression, second cancer, and incident AID using Fine–Gray regression models. Categorical variables were compared using the chi-square or Fisher's exact test, and continuous variables using the Mann–Whitney U test. Statistical analyses were performed using SPSS, JMP, and R software. Among 1968 patients with polycythemia vera (PV) or essential thrombocythemia (ET), 121 (6%) had a history of AID before/at the time of MPN diagnosis (Table 1). Compared with patients without AID, those with prior AID were older (median age 62 vs. 60 years, p = 0.016), more frequently female (69% vs. 55%, p = 0.002), and less likely to have PV (40% vs. 52%, p = 0.011). Hemoglobin levels were significantly lower in patients with AID (median 14.9 vs. 16 g/dL; p = 0.003), while platelet and leukocyte counts were similar between groups. A history of venous thrombosis at or prior to diagnosis was more frequent among patients with AID (18% vs. 12%, p = 0.046), whereas arterial thrombosis rates were comparable. Patients with previous AID more frequently had a history of other malignancies before/at MPN diagnosis (25% vs. 14%, p = 0.001), including when non-melanoma skin cancers (NMSC) were excluded (18% vs. 10%, p = 0.006). Additionally, the occurrence of subsequent AID during follow-up was more common among patients with prior AID (6% vs. 2%, p = 0.005). Among the 121 patients with AID before/at MPN diagnosis, 48 (40%) had PV and 73 (60%) had ET. Patients with PV were older (median 65 vs. 59 years, p = 0.043) and females were more common among ET cases (78% vs. 56%, p = 0.011). As expected, PV patients displayed higher hemoglobin levels, leukocyte counts, and neutrophil counts, while ET patients had higher platelet counts. Fibrotic progression was more frequent among PV cases (17% vs. 3%, p = 0.006), whereas leukemic transformation rates were low and comparable (Table S1). The spectrum of AID observed before/at and after MPN diagnosis is detailed in Figure 1A. The most frequently observed conditions included autoimmune dysthyroidism, rheumatoid arthritis, psoriasis, inflammatory bowel disease, and polymyalgia rheumatica. Kaplan–Meier analysis showed no significant difference in survival between patients with and without prior AID (log-rank p = 0.09, Figure 1B). In univariate analysis, prior AID showed a borderline association with inferior OS (HR 1.36, 95% CI 0.96–1.94, p = 0.087). After adjustment for sex, age, PV phenotype, and JAK2 mutation status, the association remained borderline and moved closer to statistical significance (HR 1.42, p = 0.054). Male sex (HR 1.50, 95% CI 1.27–1.77, p < 0.001) and increasing age (per 10 years, HR 2.43, 95% CI 2.25–2.62, p < 0.001) were independently associated with inferior survival, whereas PV (HR 1.15, p = 0.16) and JAK2 mutation status (HR 1.14, p = 0.34) were not significantly associated. To explore potential heterogeneity across AID, patients with prior AID were further stratified into two predefined categories based on the predominant clinical phenotype and anticipated degree of systemic inflammatory burden, distinguishing inflammatory arthritis, vasculitis, or unclassified AID from predominantly organ-specific, connective tissue, or inflammatory dermatosis conditions (Figure S1). In univariate analysis, patients with inflammatory arthritis, vasculitis, or unclassified AID exhibited significantly inferior survival compared with patients without AID (HR 1.89, 95% CI 1.13–3.16; p = 0.015), whereas those with organ-specific, connective tissue, or inflammatory dermatosis AID showed no significant difference (HR 1.10, 95% CI 0.69–1.77; p = 0.679). After multivariable adjustment, inflammatory arthritis/vasculitis/unclassified AID remained significantly associated with inferior survival (HR 1.64, 95% CI 1.01–2.70; p = 0.040), whereas organ-specific/connective tissue/inflammatory dermatosis AID showed no significant association (HR 1.29, 95% CI 0.80–2.08; p = 0.294). The cumulative incidence of major clinical outcomes after MPN diagnosis was assessed using competing-risk analysis (Figure S2). Prior AID was not significantly associated with MF progression (Gray test p = 0.20), AML progression (p = 0.52), venous (p = 0.49), or arterial thrombosis (p = 0.86). Conversely, a history of AID was associated with an increased risk of SC (Gray test p < 0.001, sHR 1.57, p = 0.015, Figure 2A). This association remained significant after excluding non-melanoma skin cancers (NMSC) (sHR 1.70, p = 0.022), whereas after excluding both NMSC and hematologic malignancies, only a non-significant trend was observed (sHR 1.52, p = 0.12). In the multivariable model including all cancers, prior AID was not independently associated with SC risk (sHR 1.31, 95% CI 0.88–1.96, p = 0.183) after adjustment for sex, age, PV versus ET, JAK2 mutation status, prior cancer history, hyperlipidemia, hypertension, and arterial thrombosis. Of interest, after exclusion of NMSC, prior AID showed a trend toward increased SC risk (sHR 1.50, 95% CI 0.93–2.42, p = 0.094). This association was no longer observed in the most restrictive model excluding both NMSC and hematologic malignancies (sHR 1.35, 95% CI 0.79–2.32, p = 0.276). The occurrence of incident AID after MPN diagnosis was subsequently analyzed using competing-risk methods. The cumulative incidence of AID was significantly higher among patients with prior AID compared with those without (Gray test p < 0.001, Figure 2B). In univariate analysis, prior AID (sHR 3.89, p = 0.001) and female sex (sHR 2.63, p = 0.007) were significantly associated with an increased risk of incident AID. Hypertension showed a borderline association (sHR 1.74; p = 0.095), whereas no other clinical, hematologic, or molecular variables were significantly associated (Table S2). In the multivariable model (Figure 2C), prior AID (sHR 3.03, p = 0.012), female sex (sHR 2.39, p = 0.015), and hypertension (sHR 2.18, p = 0.024) remained independently associated with an increased risk of incident AID. In this large cohort of patients with PV and ET, AID were identified in 6% of cases and were associated with a distinct clinical and comorbidity profile. Patients with prior AID were more frequently female, slightly older, and more likely to have a history of venous thrombosis and prior malignancy. These findings are consistent with previous epidemiologic studies supporting shared inflammatory and immune-mediated mechanisms across AID and myeloid neoplasia, as well as the increased risk of MPN development among patients with pre-existing AID [4, 6, 8]. Although prior AID was not significantly associated with fibrotic or leukemic progression, nor with arterial or venous thrombosis during follow-up, a borderline association with inferior survival was observed and persisted after multivariable adjustment. Exploratory analyses highlighted heterogeneity across autoimmune phenotypes, with selected AID categories demonstrating a sustained association with inferior survival [9]. Collectively, these findings support the concept that immune dysregulation and chronic inflammatory burden contribute to disease heterogeneity in MPN, influencing long-term outcomes beyond classical disease-related risk factors [3]. A history of AID was associated with an increased risk of SC in unadjusted analyses, particularly after exclusion of NMSC, although this association was attenuated after multivariable adjustment. This finding suggests that part of the observed risk may be explained by coexisting clinical factors, including prior malignancy history and cardiometabolic comorbidities, while remaining consistent with prior observations linking chronic immune dysregulation with carcinogenesis across multiple disease settings [5, 10-12]. A particularly relevant observation was the significantly increased risk of incident AID after MPN diagnosis among patients with prior AID, independent of sex, age, and hypertension. This finding aligns with the well-recognized phenomenon of polyautoimmunity, whereby individuals with one autoimmune disease have an increased risk of developing additional immune-mediated conditions over time [13, 14]. Several limitations should be acknowledged. The retrospective design introduces potential selection and ascertainment biases, and the relatively low number of specific outcomes may have limited statistical power in subgroup analyses. In addition, treatment heterogeneity across the long study period was not specifically accounted for and may have influenced clinical outcomes. Furthermore, the intrinsic heterogeneity of AID, encompassing conditions with distinct pathophysiologic mechanisms and clinical trajectories, limited the ability to evaluate outcomes for individual AID entities and required grouping into broader categories, which may have diluted subtype-specific associations. Despite these limitations, the large sample size, extended follow-up, and use of competing-risk methodology strengthen the robustness of the findings. G.G.L., N.G., and A.T. conceived and designed the study. G.G.L., F.A., M.I., P.F., M.S.R., and N.G. collected the data. G.G.L. performed statistical analyses. G.G.L. drafted the manuscript. P.G., A.M.V., A.P., N.G., and A.T. reviewed and edited the manuscript. The authors declare no conflicts of interest. The data that support the findings of this study are available from the corresponding author upon reasonable request. TABLE S1: Clinical, laboratory, and genetic characteristics at diagnosis and during follow-up in 121 patients with autoimmune or inflammatory disease before/at MPN diagnosis, stratified by polycythemia vera and essential thrombocythemia. TABLE S2: Univariate Fine–Gray regression analysis for risk of incident autoimmune or inflammatory diseases (AID) after MPN diagnosis. FIGURE S1: Overall survival according to autoimmune or inflammatory disease (AID) category. Kaplan–Meier curves comparing overall survival among patients with arthritis/vasculitis/unclassified AID, organ-specific/connective tissue disease (CTD)/dermatosis, and patients without prior AID. FIGURE S2: Cumulative incidence of major disease outcomes according to prior autoimmune or inflammatory disease (AID). Cumulative incidence curves comparing patients with prior AID versus no prior AID for (A) myelofibrosis (MF) progression, (B) acute myeloid leukemia (AML) progression, (C) venous thrombosis, and (D) arterial thrombosis. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Clinical Experience With Venetoclax-Based Combinations for Relapsed/Refractory or MRD-Positive NPM1-Mutated Acute Myeloid Leukemia Matteo Piccini, Naseema Gangat, Francesco Mannelli, Barbara Scappini, Gaia Ciolli, Francesca Crupi, Andrea Pasquini, Jessica Caroprese, Giorgio Cannetti, Chiara Lucarelli, Silvia Querceto, Giada Rotunno, Fabiana Pancani, Niccolò Bartalucci, Paola Guglielmelli, Ayalew Tefferi, Alessandro Maria Vannucchi American Journal of Hematology, 2026 NPM1 mutations occur in ~30% of acute myeloid leukemia (AML) [1] and define a distinct entity according on current WHO and ICC classification [2, 3]. NPM1mut AML shows heterogeneous clinical behavior: some patients respond well to chemotherapy with rapid measurable residual disease (MRD) clearance, while others experience primary refractoriness or early relapse. Co-mutations, particularly FLT3-ITD, contribute to this variability [4]. While first-line treatment of NPM1mut AML is well established [1], optimal management of relapsed/refractory (R/R) disease remains uncertain. Furthermore, in case of primary refractory or early relapsing patients, chemoresistance represents an issue [5]. For patients treated with curative intent, salvage chemotherapy followed by allogeneic stem cell transplantation (ASCT) is standard approach, although such regimens are burdened by toxicities that delay or prevent ASCT in some cases. In elderly and HSCT ineligible patients, therapeutic options are limited. Recently, favorable toxicity profile and efficacy of venetoclax (VEN) in combination with hypomethylating agents (HMAs) or low-dose cytarabine (LDAC) in NPM1mut AML was reported in first line [6, 7] and the R/R setting [8-10]. Moreover, considering the evolving therapeutic scenario, the role of MRD-directed intervention in NPM1mut AML, based on early detection of impending relapse at the molecular level, is unclear [11]. We retrospectively analyzed 58 adult patients with R/R or MRD-positive NPM1mut AML treated with VEN-based approaches at Careggi University Hospital, Florence (Italy) (n = 28) and Mayo Clinic, Rochester, Minnesota (US) (n = 30) between 2018 and 2025. Median age was 61.5 years (26–83); 31/58 (53.4%) patients were older than 60 years. Median follow-up duration was 26.2 months. Most patients (n = 43, 74%) were treated for relapsed disease (1st relapse, n = 35; subsequent relapse, n = 8), that in most cases occurred after CR of short duration (< 6 months, n = 27; 6–12 months, n = 9; > 12 months, n = 5; unknown, n = 2). Three patients were primary refractory. Twelve patients received VEN-based treatment as an MRD-directed approach (MRD persistence after frontline chemotherapy, n = 8; MRD relapse, n = 4). Overall, 37 patients (64%) were treated with intention-to-transplant (ITT); ultimately, 29/37 patients (78%) were able to proceed to ASCT. VEN-based treatments were mainly represented by VEN combined with HMA (n = 47/58; 81%; azacitidine, n = 30; decitabine, n = 17); other combinations including FLT3 inhibitors (FLT3i), menin inhibitors, or intensive chemotherapy. Full details of patients' characteristics and treatment regimens can be found in Table S1. Most frequently detected co-mutations were FLT3-ITDs (n = 24; 41%; median allelic ratio 0.425 (0.002–1.500)), DNMT3A (n = 23; 39%), IDH1 and IDH2 (n = 17; 31%), RAS pathway (n = 14; 24%), and FLT3-TKD (n = 6; 10%) (Figure 1 and Table S2). A total of 282 cycles were administered (with hospitalization, n = 46; 16.3%); median cycle number per patient was 4 for non-ASCT patients and 3 for HSCT recipients. Reasons for treatment discontinuation were ASCT (n = 22), treatment failure (n = 20), excessive myelotoxicity (n = 5), unknown reasons (n = 4), medical decision (n = 3), infection (n = 1), death due to unrelated cause (n = 1). At the time of data cut-off, two patients were still receiving treatment. Overt R/R cohort: composite CR rate (CCR; CR + CR with incomplete counts recovery) was 65.2% (30/46), with 17/46 (36.9%) patients achieving CR and 13/46 (28.3%) CRi status. About 70% of complete responders achieved MRD negativity in bone marrow (BM) and/or peripheral blood (PB) by RT-qPCR (or flow cytometry, in case of noncanonical mutant NPM1 transcripts). Best response occurred early during treatment (cycle 1, n = 20; cycle 2, n = 4; cycle 3, 4, and 6, n = 1; unknown, n = 3). No genetic biomarker (including aberrant karyotype, FLT3-ITD status, IDH1/2 status, RAS pathway mutations) or prior exposure to HMA or FLT3i influenced CR probability (Table S3). Patients with FLT3 mutation (ITD or TKD) had a CCR of 63.6% (14/22; CR, n = 6; CRi, n = 8); restricting the analysis to FLT3-ITD cases, CCR was 55.5% (10/18; CR, n = 2/10; CRi, n = 8/10). Prior FLT3i exposure did not reduce CCR in FLT3-mutated patients. Eighteen of 25 (72%) patients treated with ITT were able to proceed to ASCT. Median OS and EFS was 20.7 and 13 months, respectively (Figures 2 and 3). IDH1 or IDH2 mutation was associated with longer, though not statistically significant, EFS (45.7 vs. 9.7 months, p = 0.137) and OS (24.5 vs. 9.5 months; p = 0.064). Conversely, FLT3-ITD positivity was associated with shorter EFS (9.5 vs. 13.9 months) and OS (9.5 vs. 24.5 months). Patients undergoing had significantly longer EFS (26.8 vs. 5.7 months; p = 0.048) and OS (median not reached vs. 9.5 months; p = 0.013). A survival plateau for both EFS and OS was observed, with seven patients experiencing long-term survival at data cut (five off treatment). In multivariate analysis, both IDH1/2 mutation and ASCT were independently associated with improved outcomes. IDH1/2 mutation was associated with a > three-fold reduction in risk of death (OS: HR 0.324; 95% CI, 0.108–0.968; p = 0.043) and a nonsignificant reduction in event risk (EFS: HR 0.400; 95% CI, 0.146–1.097; p = 0.075). ASCT was significantly associated with improved OS (HR: 0.267; 95% CI: 0.103–0.690; p = 0.006) and EFS (HR: 0.371; 95% CI: 0.103–0.885; p = 0.025) (Table S4). MRD relapse/persistence cohort: All patients achieved complete MRD clearance by RT-qPCR, including 7 with FLT3 mutations (FLT3-TKD, n = 1; FLT3-ITD, n = 6). Best response occurred at cycle 1 in 5 patients, cycle 2 in 3, cycle 3 in 3, and cycle 4 in 1. All patients were successfully bridged to ASCT, except for a 57-year-old woman diagnosed with end-stage cholangiocarcinoma (Table S3). Median OS and EFS were not reached (Figure 3), and most OS events were due to transplant-related mortality. The safety profile was consistent with previous reports, with no treatment-related deaths. Nonhematologic adverse events are reported in Table S5. Notably, in the MRD relapse/persistence cohort, VEN-based regimens (VEN-AZA, n = 9; VEN-AZA + ziftomenib, n = 2; VEN + gilteritinib, n = 1) were particularly well tolerated, with cytopenias (mainly neutropenia) as the most frequent treatment-related AE and only one case of G3 febrile neutropenia. To our knowledge, this represents one of the largest series evaluating outcomes of R/R and MRD positive NPM1mut AML patients treated with VEN-based combinations. The observed CCR rate is comparable to that reported for conventional salvage regimens in R/R AML patients [12], including NPM1mut cases, despite most patients in our cohort would being ineligible for intensive chemotherapy due to age or comorbidities and having short prior CR duration, a setting typically associated with poor outcomes. Although the study was not powered to assess the impact of co-mutations on CR achievement and survival, improved outcomes were observed in patients with IDH1 or IDH2 mutations, consistent with previous reports [7, 9, 10]. In FLT3mut patients, while FLT3 inhibitor-based regimens remain preferred, VEN-based approaches may represent a potential option. Notably, patients treated for MRD relapse or persistence achieved high MRD clearance and favorable survival. The tolerability and activity of VEN-based regimens support their potential role in MRD-directed therapy, currently being investigated in a phase II GIMEMA (Gruppo Italiano Malattie Ematologiche dell'Adulto) trial (NCT04867928). The favorable toxicity profile of VEN-based regimens may offer an advantage over conventional salvage chemotherapy, particularly as bridge-to-transplant in R/R NPM1mut AML. Interestingly, the durable CRs were observed in some patients even without ASCT, warranting further investigation. This work received funding from “Fondo Zottola”, University of Florence. This study was reviewed and approved by the Institutional Review Board (Comitato Etico Area Vasta Centro—CEAVC). Written informed consent was obtained by patients according to the Declaration of Helsinki. M.P.: Speaker bureau AbbVie Pharmaceuticals, Astellas, Astrazeneca, SERB, Amgen, Incyte. N.G.: Advisory Board for DISC Medicine and Agios. F.M.: Speaker bureau Blueprint, Novartis, Abbvie, Servier, GSK, Astellas. A.M.V.: honoraria from AbbVie, Novartis, Blueprint, GSK. The data that support the findings of this study are available from the corresponding author upon reasonable request. Table S1: Clinical and demographic characteristics of the study population. CR, complete remission; FLT3i, FLT3 inhibitor; HSCT, hematopoietic stem cell transplantation; ITD, internal tandem duplication; ITT, intention-to-transplant; MRD, minimal residual disease; TKD, tyrosine kinase domain; VEN, venetoclax. Table S2: Cytogenetic and molecular characteristics of the whole patient population. Full details regarding co-mutations can be found in Figure 1. Table S3: Response rates and kinetics with VEN-based regimens and HSCT bridging data in relapsed/refractory and MRD-positive patients sub-cohorts. CCR, composite complete remission; CR, complete remission; CRi, complete remission with incomplete counts recovery; FLT3i, FLT3 inhibitor; HMA, hypomethylating agent; HSCT, hematopoietic stem cell transplantation; ITT, intention-to-transplant; MRD, minimal residual disease. Table S4: Survival data according to relevant clinical and molecular covariates. EFS, event-free survival. HSCT, hematopoietic stem cell transplantation. HR, hazard ratio. OS, overall survival. Table S5: Nonhematological adverse events (whole cohort). Grading according to common terminology criteria for adverse events (CTCAE) version 5.0. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Describing the use of ruxolitinib for the treatment of myelofibrosis: a plain language summary of the ROMEI early study results Massimo Breccia, Paola Guglielmelli, Chiara Castiglioni, Francesca Palandri, Francesco Passamonti Future Oncology London England, 2026 What is this summary about? This plain language summary describes the first results obtained from the ROMEI study. In this study, researchers want to learn how doctors in Italy use ruxolitinib to treat people with myelofibrosis, a rare type of blood cancer. It also looks at how ruxolitinib affects the symptoms and overall health of participants. What are the key takeaways? Out of 306 participants, 57% received the expected dose of ruxolitinib, based on their blood test results. Conversely, 43% started with a lower dose than expected, even though their blood test results would have allowed a higher dose. Before the start of the study, people who received the expected dose of ruxolitinib (the ‘AsEx group’) were generally younger and showed better blood test results than participants who received a lower-than-expected dose (the ‘LtEx group’). During the first 12 months of the treatment, participants in the AsEx group were treated with ruxolitinib for a longer time with fewer interruptions compared to participants in the LtEx group. They also felt better sooner and had a greater, faster reduction in the size of their spleen. Fewer people in the AsEx group died compared to the LtEx group. What were the main conclusions reported by the researchers? Patients who received the expected dose of ruxolitinib showed greater improvements in their health compared to those who received a lower dose. Some physicians started with lower doses for older or more frail patients. However, in this study, starting at a lower dose did not show additional advantages. What do the results mean and why does it matter? These results show how important it is to start ruxolitinib at the right dose, based on each person’s blood test results. Starting at the right dose can help people with myelofibrosis get the best possible results from treatment, such as faster relief from symptoms, reduction of spleen size, and possibly a longer life.
Artificial intelligence differentiates prefibrotic primary myelofibrosis with thrombocytosis from essential thrombocythemia using digitized bone marrow biopsy images Andrew Srisuwananukorn, Giuseppe Gaetano Loscocco, James M. Dolezal, Andrew T. Kuykendall, Raffaella Santi, Ling Zhang, Avani M. Singh, Paola Guglielmelli, Alessandro Maria Vannucchi, Mohamed E. Salama, Alexander T. Pearson, Ronald Hoffman Leukemia, 2026 Prefibrotic primary myelofibrosis (prePMF) and essential thrombocythemia (ET) are distinct myeloproliferative neoplasms (MPNs) with overlapping clinical features, often leading to diagnostic uncertainty. We developed an artificial intelligence (AI) framework with human interpretability to distinguish prePMF from ET using digitized hematoxylin and eosin-stained bone marrow biopsy (BMB) slides. Trained on an initial cohort of MPN patients with thrombocytosis, the AI model achieved an AUROC of 0.89 and accuracy of 92.3%. To assess the image features guiding predictions, we generated synthetic images which potentially exaggerate disease-specific morphologies. In a blinded survey, hematopathologists reviewed both real and AI-generated images. While human experts frequently agreed with AI predictions on diagnosis with real images, diagnostic discordance reached up to 88% for AI-generated ET images despite being correctly predicted by AI. We further quantified marrow cellularity and adiposity in the real and generated images, which revealed a higher proportion of fat content in all ET images (42.0%) compared to prePMF (28.9%). These findings suggest that AI can utilize morphological cues distinct from current established diagnostic criteria, such as proportion of adiposity to distinguish types of MPNs. Thus, an AI-assisted diagnostic tool underscores the potential of AI to augment histopathologic evaluation and allow identification of more specific subpopulations of forms of MPNs.
APL-like subset within NPM1-mutated AML: A distinct immunophenotype correlating with early vascular complications Francesco Mannelli, Francesca Crupi, Sara Bencini, Michaela Feuring, Gaia Ciolli, Matteo Piccini, Marco Frigeni, Raffaele Palmieri, Chiara Sartor, Barbara Scappini, Giacomo Gianfaldoni, Benedetta Peruzzi, Roberto Caporale, Antonio Scannella, Laura Fasano, Elisa Quinti, Andrea Pasquini, Jessica Caroprese, Leonardo Signori, Fabiana Pancani, Chiara Maccari, Tiziana Ottone, Daniela Spaeth, Antonio Curti, Maria Teresa Voso, Francesco Annunziato, Konstanze Döhner, Adriano Venditti, Francesco Buccisano, Alessandro Rambaldi, Paola Guglielmelli, Hartmut Döhner, Alessandro M. Vannucchi Hemasphere, 2026 Among NPM1 ‐mutated acute myeloid leukemia (AML) ( NPM1 mut ), a distinct subtype has been described with an immunophenotypic profile resembling acute promyelocytic leukemia (APL‐like). In this retrospective multicenter study including 384 NPM1 mut AML patients, we identified 95 (24.7%) cases exhibiting an APL‐like immunophenotype. This subset was characterized by significant abnormalities in coagulopathy markers (D‐dimer, D‐dimer/fibrinogen ratio, and disseminated intravascular coagulation [DIC] score). The cumulative incidence of vascular events at 30 days was significantly higher in the APL‐like group compared to the non‐APL‐like group (30.5% vs. 10.1%, P < 0.001). Notably, a higher cumulative incidence of early death due to vascular complications (within 30 days) was observed in the APL‐like group (6.3% vs. 0.35% in controls; P = 0.00015). In multivariate analysis, the APL‐like immunophenotype was the only significant factor associated with vascular‐related early death (hazard ratio [HR] = 19, P = 0.0063). There was a significantly higher rate of IDH1/2 mutations in APL‐like (68.3%) compared to non‐APL‐like (18.3%, P < 0.001) cases. We validated these clinical and molecular findings in an independent validation cohort of 302 NPM1 mut patients enrolled in the acute myeloid leukemia study group (AMLSG) 09‐09 clinical trial, which included the administration of all‐trans retinoic acid (ATRA) to all patients and a randomization for gemtuzumab ozogamicin. In this cohort, the APL‐like immunophenotype was associated with events occurring within the first 15 days but did not influence mortality, likely due to protocol‐driven patient selection. Our findings have important clinical implications that warrant the development of studies exploring disease‐tailored clinical measures to mitigate the risk of early vascular events, as in current APL management.
ONE HUNDRED SUSPECTED MYELOPROLIFERATIVE NEOPLASMS WITH A JAK2 V617F VARIANT ALLELE FREQUENCY <2%: CLINICAL, GENETIC AND HISTOPATHOLOGICAL CORRELATES Giuseppe Gaetano Loscocco Haematologica, 2026 Introduction. JAK2 V617F (JAK2) is the most frequent driver mutation in myeloproliferative neoplasms (MPN), but it was found in healthy individuals with clonal hematopoiesis of indeterminate potential (CHIP), though its role in CHIP remains debated (Leukemia 2021;35(9):2706-2709). We examined clinical, genetic, and morphological features in suspected MPN cases with JAK2 VAF <2%. Methods. We included 100 suspected MPN cases with JAK2 VAF <2% (2010–2025). After excluding secondary causes, patients were grouped as follows: erythrocytosis (n=35), thrombocytosis (n=47), and miscellaneous (n=18; detailed in Figure 1). All samples and data were collected at diagnosis. JAK2 VAF was assessed in granulocytes by dd-PCR (limit of detection 0.01%); BM biopsies were reviewed by R.S. and U.G. (Blood 2022; 140(11):1200-1228).Results. Overall, median age was 62 years, male 64%, median JAK2 VAF 0.22%. Median (range) leukocyte count was 7.6 x 109/L (5-30), hemoglobin 14.6 g/dL (9-19.5), hematocrit 43.5% (28-57), platelets 408x109/L (98-1450). Previous history of venous and arterial thrombosis in 10%/12%, respectively. No age differences among 3 groups (p=0.8), whereas patients with erythrocytosis were mostly male (91% vs. 42% vs. 67%, p<0.01), EPO value subnormal in only 1 case. Driver mutations other than JAK2 were documented in 33 patients: 24 CALR comprising type-1 (n=17), type-2 (n=5), atypical (n=2) and 9 MPL (7 at p.W515 and 2 at p.S505). Of note, double driver mutated cases constituted 68% of all those with thrombocytosis. Respective median VAF for CALR /MPL mutations were 34%/21%. Considering patients with thrombocytosis, those with JAK2 only vs. double mutated were mostly ET (93% vs. 60%, p=0.03), had lower platelets (546 vs. 845x109 /L, p<0.01), and higher JAK2 VAF (0.55 vs. 0.15%, p=0.04). Additional NGS mutations were reported in 24 (52%) cases, mostly, in miscellaneous group (75%, p=0.2); overall, the most represented were ASXL1 (13%), TET2 (7%), SH2B3 (7%), KIT (7%), DNMT3A (7%), NF1 (7%) mutations. 9% showed abnormal karyotypes (7 cases –Y, 1 case -22, 1 case +13), with similar distribution across the groups. Considering patients with erythrocytosis, BM histologic features were consistent with PV in 8 cases whereas the other 27 cases showed age-adjusted normal/focally increased cellularity, regular/mildly expanded erythroid lineage consistent with a diagnosis of MPN unclassifiable (MPN-U). Among patients with thrombocytosis and miscellaneous group, diagnosis are reported in Figure 1. Conclusions. This study underscores the significance of employing highly sensitive assays for the detection of JAK2, as well as emphasises the necessity of concurrent screening for CALR and MPL mutations in patients presenting with thrombocytosis and low JAK2 VAF. In those with erythrocytosis, early histopathological signs of MPN can be subtle, so integrating histopathology with clinical and genetic data is essential for an appropriate diagnosis.
MOLECULAR CHARACTERIZATION OF A COHORT OF PATIENTS WITH POLYCYTHEMIA VERA: A SINGLE-CENTER STUDY Elena Nacca Haematologica, 2026 Introduction. Polycythemia vera (PV) is a chronic myeloproliferative neoplasm mainly driven by JAK2 mutations. Additional myeloid gene mutations (MyMut) have been reported, sometimes with prognostic relevance, but the molecular landscape at diagnosis and its impact on disease phenotype or outcome remain unclear.Methods. We included patients (pts) with a diagnosis (dx) of PV according to WHO/ICC 2022 criteria with at least a DNA sample collected at dx or during the chronic phase in the absence of disease progression, and with comprehensive hematologic, clinical, and outcome data. Molecular and bioinformatic analyses were performed using a targeted NGS panel (SOPHiA DDM Myeloid Solution) on the SOPHiA DDM platform.Results. A total of 637 PV pts were analyzed, 355 (55.7%) were males with a median age of 61.3 years (range 14.4–91.8). 138 pts (21.7%) progressed to post-PV Myelofibrosis (MF), 15 (2.4%) to blast phase (BP) during the PV chronic phase, 222 (34.9%) pts had at least an event of thrombosis (138 (62.2%) at dx or within the 5 preceding years, and 109 (49.1%) during follow-up), including both arterial (n=121) and venous (n=125). Death occurred in 109 (17.1%). Almost all pts (99.4%) harbored a JAK2 mutation: JAK2 V617F in 625 (98.1%) cases and JAK2 exon 12 mutations in 8 (1.3%). 4 pts resulted JAK2 WT. Additionally, 11 pts (10 V617F, 1 exon 12) harbored a JAK2 mutation combined with a non-canonical JAK2 variant. Other MyMut were found in 283 pts (44.4%), with 8.9%, and 2.4% of pts harboring 2 or ≥3 mutations, respectively. JAK2-negative pts showed mutations in ASXL1 (n=1), DNMT3A (n=1) and ZRSR2 (n=1). The most frequently mutated genes (≥5 pts) were: TET2 (21.4%, mean VAF 23.9%), ASXL1 (12%, mean VAF 24.4%), DNMT3A (9.9%, mean VAF 17.8%).The most common co-mutation patterns were: 9.4% pts carried both TET2 and ASXL1 mutations, 8% TET2 and DNMT3A, 4.8% ASXL1 and EZH2, 5.8% ASXL1 and IDH2.Correlation analyses showed that the presence of at least 1 MyMut correlates with worst prognosis, as shown in Figure 1. In particular, genes more significantly associated with shortened overall survival (OS) were DNMT3A (p=0.012), TET2 (p<0.001) and U2AF1 (p=0.002). In addition, ASXL1 (p<0.001), and EZH2 (p=0,002) were associated with progression to secondary myelofibrosis –postPV, while DNMT3A (p<0.001) resulted inversely correlated with MF progression. Conclusions. These findings demonstrate that almost half of PV pts show a complex molecular landscape already at diagnosis, and that both survival and progression to MF may be influenced by the presence of additional mutations in myeloid-associated genes. Comprehensive molecular profiling at diagnosis may improve risk stratification and future prognostic models in PV.
Clinical Outcomes of Ruxolitinib Treatment in Patients With IPSS Intermediate-1-Risk Myelofibrosis: Interim Analysis From an Italian, Prospective Study (ROMEI) Paola Guglielmelli, Massimo Breccia, Francesco Mendicino, Maurizio Martelli, Nicola Di Renzo, Giuseppe A. Palumbo, Monica Crugnola, Maurizio Musso, Silvia Sibilla, Paolo Sportoletti, Elisabetta Abruzzese, Stefana Impera, Alessandra Malato, Sergio Siragusa, Carmine Selleri, Fabrizio Pane, Bruno Martino, Alessandra Ricco, Angelo Gardellini, Anna Marina Liberati, Agostino Tafuri, Maria Langella, Marco Brociner, Paolo Ditonno, Domenico Pastore, Olga Mulas, Barbara Pocali, Marco De Gobbi, Erika Morsia, Giulia Benevolo, Elena Maria Elli, Valerio De Stefano, Antonietta Pia Falcone, Daniele Vallisa, Simona Tomassetti, Francesca Lunghi, Nicola Orofino, Giuseppe Carli, Tiziana Urbano, Alessandro Lucchesi, Marta Brunoventre, Massimiliano Bonifacio, Gianni Binotto, Francesco Cavazzini, Paola Ranalli, Alessandro Allegra, Barbara Anaclerico, Serena Mazzotta, Filippo Gherlinzoni, Mario Tiribelli, Chiara Castiglioni, Marina Landoni, Diletta Valsecchi, Michela Magnoli, Francesco Passamonti, Francesca Palandri Hematological Oncology, 2026
Health Care Utilization Databases obtained from health system inform outcome for ruxolitinib treatment in patients with myelofibrosis Barbara Mora, Matteo Franchi, Ludovica Margotto, Olivia Leoni, Daniela D'ippoliti, Emanuela Carloni, Ilaria Cozzi, Enrica Santelli, Fabrizio Gemmi, Claudia Szasz, Margherita Maffioli, Carmelo Gurnari, Enrico Attardi, Daniele Cattaneo, Marta Bortolotti, Nicola Stefano Fracchiolla, Alessandra Iurlo, Giovanni Corrao, Matteo Giovanni Della Porta, Alessandro Maria Vannucchi, Maria Teresa Voso, Paola Guglielmelli, Francesco Passamonti Hemasphere, 2026
Genomic profiling for decision-making in post–polycythemia vera and post–essential thrombocythemia myelofibrosis Barbara Mora, Francesca Palandri, Paola Guglielmelli, Andrew T. Kuykendall, Margherita Maffioli, Alessandra Iurlo, Valerio De Stefano, Silvia Salmoiraghi, Timothy Devos, Federico Itri, Francisco Cervantes, Jean-Jacques Kiladjian, Matteo G. Della Porta, Francesco Albano, Jason Gotlib, Giulia Benevolo, Marianna Caramella, Marco Ruggeri, Elisa Rumi, David M. Ross, Chiara Pessina, Ilaria Colugnat, Francesco Orsini, Giorgia Micucci, Giada Rotunno, Rami S. Komrokji, Daniele Cattaneo, Patrizia Chiusolo, Marta Bortolotti, Tiziano Barbui, Daniela Cilloni, Massimo Breccia, Giuseppe A Palumbo, Filippo Branzanti, Ludovica Margotto, Matteo Franchi, Alessandro M. Vannucchi, Francesco Passamonti Blood, 2026
Genome-wide analysis defines genetic determinants of MPN subtypes and identifies a sex-specific association at CDH22/CD40 William J. Tapper, Ahmed A. Z. Dawoud, Joannah Score, Andrew J. Chase, E. Joanna Baxter, Joanne Ewing, Louise Wallis, Paola Guglielmelli, Dolors Colomer, Beatriz Bellosillo, Montse Gomez, Juan Carlos Hernández-Boluda, Carlos Besses, Francisco Cervantes, Steffen Koschmieder, Anthony R. Green, Andreas Reiter, Alessandro Vannucchi, Claire Harrison, Nicholas C. P. Cross Blood, 2025
Impact of baseline genetic profile and treatment on outcome and hematological toxicity in CEBPA-mutated AML Francesco Mannelli, Matteo Piccini, Marco Frigeni, Giacomo Gianfaldoni, Sara Bencini, Silvia Salmoiraghi, Barbara Scappini, Benedetta Peruzzi, Roberto Caporale, Gaia Ciolli, Francesca Crupi, Laura Fasano, Elisa Quinti, Andrea Pasquini, Jessica Caroprese, Fiorenza Vanderwert, Giada Rotunno, Fabiana Pancani, Leonardo Signori, Danilo Tarantino, Chiara Maccari, Francesco Annunziato, Orietta Spinelli, Paola Guglielmelli, Alessandro Rambaldi, Alessandro M. Vannucchi Blood Cancer Journal, 2025
Triple A Plus (AAA+) Survival Prediction Model for Essential Thrombocythemia: Analysis Involving 7308 Patients Ayalew Tefferi, Giuseppe G. Loscocco, Lior Rokach, Tamar Tadmor, Priyansh Faldu, Guy Melamed, Hilel Alapi, Maymona Abdelmagid, Rania M. Abdelaziz, Muhammad Yousuf, Merry Nakhleh, Animesh Pardanani, Kebede H. Begna, Mirnal M. Patnaik, Natasha Szuber, Alessandra Carobbio, Tiziano Barbui, Kaaren K. Reichard, Rong He, Paola Guglielmelli, Naseema Gangat, Alessandro M. Vannucchi American Journal of Hematology, 2025
Exploring thromboembolic risk factors in polycythemia vera: from current evidence to PROSPERO study design Valerio De Stefano, Francesco Passamonti, Francesca Palandri, Francesco Ramundo, Elena Rossi, Silvia Betti, Lorenzo Fagiolo, Paola Guglielmelli, Davide Pio Abagnale, Novella Pugliese, Daniele Cattaneo, Alessandra Iurlo, Filippo Branzanti, Alessandra Dedola, Hillary Catellani, Alessia Tieghi, Marco Basso, Elisabetta Calistri, Elena Maria Elli, Elena Masselli, Erika Morsia, Giulia Benevolo, Massimo Breccia, Vincenza de Fazio, Maria Di Perna, Monia Marchetti, Marco Santoro, Agostino Tafuri, Chiara Castiglioni, Chiara Rotella, Sergio Siragusa, Alessandro Maria Vannucchi, and Annals of Hematology, 2025
Role of allo-HCT in “nonclassical” MPNs and MDS/MPNs: recommendations from the PH&G Committee and the CMWP of the EBMT Nicola Polverelli, Juan Carlos Hernandez-Boluda, Francesco Onida, Carmelo Gurnari, Kavita Raj, Tomasz Czerw, Michelle Kenyon, Marie Robin, Katja Sockel, Annalisa Ruggeri, Isabel Sánchez-Ortega, Daniel A. Arber, Luca Arcaini, Fernando Barroso Duarte, Giorgia Battipaglia, Yves Chalandon, Fabio Ciceri, Nicholas C.P. Cross, Joanna Drozd-Sokolowska, Vaneuza Araújo Moreira Funke, Nico Gagelmann, Naseema Gangat, Jason Gotlib, Paola Guglielmelli, Claire N. Harrison, Gabriela S Hobbs, Tania Jain, Joseph D. Khoury, Jean-Jacques Kiladjian, Nicolaus Kröger, Luca Malcovati, Massimo Martino, Ruben Mesa, Attilio Orazi, Eric Padron, Francesca Palandri, Francesco Passamonti, Mrinal M. Patnaik, Naveen Pemmaraju, Deepti H. Radia, Andreas Reiter, Domenico Russo, Christof Scheid, Ayalew Tefferi, Alessandro M. Vannucchi, Daniel Howard Wiseman, Ibrahim Yakoub-Agha, Donal P McLornan Blood, 2025
TP53 Mutations in Myeloproliferative Neoplasms: Context-Dependent Evaluation of Prognostic Relevance Ayalew Tefferi, Maymona Abdelmagid, Giuseppe G. Loscocco, Saubia Fathima, Kebede H. Begna, Aref Al‐Kali, James Foran, Jeanne Palmer, Talha Badar, Mrinal M. Patnaik, Kaaren K. Reichard, Rong He, Cinthya J. Zepeda Mendoza, Mithun Shah, Attilio Orazi, Daniel A. Arber, Animesh Pardanani, Alessandro M. Vannucchi, Devendra Hiwase, Naseema Gangat, Paola Guglielmelli American Journal of Hematology, 2025
Dosing and clinical outcomes of ruxolitinib in patients with myelofibrosis in a real-world setting: Interim results of the Italian observational study (ROMEI) Massimo Breccia, Francesca Palandri, Maurizio Martelli, Francesco Mendicino, Alessandra Malato, Giuseppe A. Palumbo, Silvia Sibilla, Nicola Di Renzo, Elisabetta Abruzzese, Sergio Siragusa, Monica Crugnola, Carmine Selleri, Fabrizio Pane, Paolo Sportoletti, Bruno Martino, Stefana Impera, Alessandra Ricco, Maria Langella, Paolo Ditonno, Giuseppe Carli, Federico Itri, Anna Marina Liberati, Tiziana Urbano, Agostino Tafuri, Vita Polizzi, Domenico Pastore, Erika Morsia, Giulia Benevolo, Giorgia Micucci, Gabriella Farina, Massimiliano Bonifacio, Elena Maria Elli, Angelo Gardellini, Valerio De Stefano, Giovanni Caocci, Antonietta Pia Falcone, Daniele Vallisa, Marco Brociner, Mario Tiribelli, Gianni Binotto, Barbara Pocali, Francesco Cavazzini, Simona Tomassetti, Francesca Lunghi, Mauro Di Ianni, Alessandro Allegra, Barbara Anaclerio, Serena Mazzotta, Nicola Orofino, Filippo Gherlinzoni, Chiara Castiglioni, Marina Landoni, Diletta Valsecchi, Michela Magnoli, Paola Guglielmelli, Francesco Passamonti Cancer, 2025
Essential Thrombocythemia: A Review Ayalew Tefferi, Naseema Gangat, Giuseppe Gaetano Loscocco, Paola Guglielmelli, Natasha Szuber, Animesh Pardanani, Attilio Orazi, Tiziano Barbui, Alessandro Maria Vannucchi JAMA, 2025
When and how to transplant in myelofibrosis–recent trends Naman Sharma, Giuseppe G. Loscocco, Naseema Gangat, Paola Guglielmelli, Animesh Pardanani, Alessandro M. Vannucchi, Hassan B. Alkhateeb, Ayalew Tefferi, Vincent T. Ho Leukemia and Lymphoma, 2025
Proposals for revised International Working Group–European LeukemiaNet criteria for anemia response in myelofibrosis Ayalew Tefferi, Giovanni Barosi, Francesco Passamonti, Juan Carlos Hernandez-Boluda, Prithviraj Bose, Konstanze Döhner, Martin Ellis, Naseema Gangat, Jacqueline S. Garcia, Heinz Gisslinger, Jason Gotlib, Paola Guglielmelli, Vikas Gupta, Claire N. Harrison, Elizabeth O. Hexner, Gabriela S Hobbs, Jean-Jacques Kiladjian, Steffen Koschmieder, Nicolaus Kröger, Andrew T Kuykendall, Giuseppe Gaetano Loscocco, John O. Mascarenhas, Lucia Masarova, Ruben Mesa, Barbara Mora, Olatoyosi Odenike, Stephen T. Oh, Animesh D Pardanani, Anand A Patel, Naveen Pemmaraju, Alessandro Rambaldi, Raajit K. Rampal, Shireen Sirhan, Natasha Szuber, Moshe Talpaz, Pankit Vachhani, Alessandro M. Vannucchi, Tiziano Barbui Blood, 2024
Targeting exhausted cytotoxic T cells through CTLA-4 inhibition promotes elimination of neoplastic cells in human myelofibrosis xenografts Lara Tavernari, Sebastiano Rontauroli, Ruggiero Norfo, Margherita Mirabile, Monica Maccaferri, Barbara Mora, Elena Genovese, Sandra Parenti, Chiara Carretta, Elisa Bianchi, Matteo Bertesi, Francesca Pedrazzi, Elena Tenedini, Silvia Martinelli, Maria Teresa Bochicchio, Paola Guglielmelli, Leonardo Potenza, Alessandro Lucchesi, Francesco Passamonti, Enrico Tagliafico, Mario Luppi, Alessandro Maria Vannucchi, Rossella Manfredini, and American Journal of Hematology, 2024
Chromosome 9p trisomy increases stem cells clonogenic potential and fosters T-cell exhaustion in JAK2-mutant myeloproliferative neoplasms Chiara Carretta, Sandra Parenti, Matteo Bertesi, Sebastiano Rontauroli, Filippo Badii, Lara Tavernari, Elena Genovese, Marica Malerba, Elisa Papa, Samantha Sperduti, Elena Enzo, Margherita Mirabile, Francesca Pedrazzi, Anita Neroni, Camilla Tombari, Barbara Mora, Margherita Maffioli, Marco Mondini, Marco Brociner, Monica Maccaferri, Elena Tenedini, Silvia Martinelli, Niccolò Bartalucci, Elisa Bianchi, Livio Casarini, Leonardo Potenza, Mario Luppi, Enrico Tagliafico, Paola Guglielmelli, Manuela Simoni, Francesco Passamonti, Ruggiero Norfo, Alessandro Maria Vannucchi, Rossella Manfredini, and Leukemia, 2024
Clinical impact of mutated JAK2 allele burden reduction in polycythemia vera and essential thrombocythemia Paola Guglielmelli, Barbara Mora, Francesca Gesullo, Francesco Mannelli, Giuseppe Gaetano Loscocco, Leonardo Signori, Chiara Pessina, Ilaria Colugnat, Raffaela Aquila, Manjola Balliu, Chiara Maccari, Simone Romagnoli, Chiara Paoli, Elena Nacca, Lorenzo Fagiolo, Margherita Maffioli, Tiziano Barbui, Francesco Passamonti, Alessandro M. Vannucchi American Journal of Hematology, 2024
Long-term pharmacodynamic and clinical effects of twice- versus once-daily low-dose aspirin in essential thrombocythemia: The ARES trial Bianca Rocca, Alberto Tosetto, Giovanna Petrucci, Elena Rossi, Silvia Betti, Denise Soldati, Alessandra Iurlo, Daniele Cattaneo, Cristina Bucelli, Alfredo Dragani, Mauro Di Ianni, Paola Ranalli, Francesca Palandri, Nicola Vianelli, Eloise Beggiato, Giuseppe Lanzarone, Marco Ruggeri, Giuseppe Carli, Elena Maria Elli, Rossella Renso, Maria Luigia Randi, Irene Bertozzi, Giuseppe Gaetano Loscocco, Alessandra Ricco, Giorgina Specchia, Alessandro M. Vannucchi, Francesco Rodeghiero, Valerio De Stefano, Carlo Patrono, and American Journal of Hematology, 2024
ROP-ET: a prospective phase III trial investigating the efficacy and safety of ropeginterferon alfa-2b in essential thrombocythemia patients with limited treatment options Jean-Jacques Kiladjian, Francisca Ferrer Marin, Haifa Kathrin Al-Ali, Alberto Alvarez-Larrán, Eloise Beggiato, Maria Bieniaszewska, Massimo Breccia, Veronika Buxhofer-Ausch, Olga Cerna, Ana-Manuela Crisan, Catalin Doru Danaila, Valerio De Stefano, Konstanze Döhner, Victoria Empson, Joanna Gora-Tybor, Martin Griesshammer, Sebastian Grosicki, Paola Guglielmelli, Valentin García-Gutierrez, Florian H. Heidel, Arpád Illés, Ciprian Tomuleasa, Chloe James, Steffen Koschmieder, Maria-Theresa Krauth, Kurt Krejcy, Mihaela-Cornelia Lazaroiu, Jiri Mayer, Zsolt György Nagy, Franck-Emmanuel Nicolini, Francesca Palandri, Vassiliki Pappa, Andreas Johannes Reiter, Tomasz Sacha, Stefanie Schlager, Stefan Schmidt, Evangelos Terpos, Martin Unger, Albert Wölfler, Blanca Xicoy Cirici, Christoph Klade Annals of Hematology, 2024
CALR mutation burden in essential thrombocythemia and disease outcome Paola Guglielmelli, Natasha Szuber, Naseema Gangat, Giulio Capecchi, Chiara Maccari, Michaël Harnois, Omer Karrar, Maymona Abdelmagid, Manjola Balliu, Elena Nacca, Alessandro Atanasio, Ilaria Sestini, Audrey Desilets, Giuseppe Gaetano Loscocco, Giada Rotunno, Lambert Busque, Ayalew Tefferi, Alessandro Maria Vannucchi Blood, 2024
Functional relevance of circRNA aberrant expression in pediatric acute leukemia with KMT2A::AFF1 fusion Caterina Tretti Parenzan, Anna Dal Molin, Giorgia Longo, Enrico Gaffo, Alessia Buratin, Alice Cani, Elena Boldrin, Valentina Serafin, Paola Guglielmelli, Alessandro M. Vannucchi, Giovanni Cazzaniga, Andrea Biondi, Franco Locatelli, Lueder H. Meyer, Barbara Buldini, Geertruij te Kronnie, Silvia Bresolin, Stefania Bortoluzzi Blood Advances, 2024
Ropeginterferon phase 2 randomized study in low-risk polycythemia vera: 5-year drug survival and efficacy outcomes Tiziano Barbui, Alessandra Carobbio, Valerio De Stefano, Alberto Alvarez-Larran, Arianna Ghirardi, Greta Carioli, Francesca Fenili, Elena Rossi, Fabio Ciceri, Massimiliano Bonifacio, Alessandra Iurlo, Francesca Palandri, Giulia Benevolo, Fabrizio Pane, Alessandra Ricco, Giuseppe Carli, Marianna Caramella, Davide Rapezzi, Caterina Musolino, Sergio Siragusa, Elisa Rumi, Andrea Patriarca, Nicola Cascavilla, Barbara Mora, Emma Cacciola, Laura Calabresi, Giuseppe Gaetano Loscocco, Paola Guglielmelli, Francesca Gesullo, Silvia Betti, Francesco Ramundo, Francesca Lunghi, Luigi Scaffidi, Cristina Bucelli, Daniele Cattaneo, Nicola Vianelli, Marta Bellini, Maria Chiara Finazzi, Gianni Tognoni, Alessandro Rambaldi, Alessandro Maria Vannucchi Annals of Hematology, 2024
Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis Paola Guglielmelli, Chiara Maccari, Benedetta Sordi, Manjola Balliu, Alessandro Atanasio, Carmela Mannarelli, Giulio Capecchi, Ilaria Sestini, Giacomo Coltro, Giuseppe Gaetano Loscocco, Giada Rotunno, Eva Angori, Filippo C. Borri, Ayalew Tefferi, Alessandro M. Vannucchi Blood Cancer Journal, 2023
Clonal dynamics and copy number variants by single-cell analysis in leukemic evolution of myeloproliferative neoplasms Laura Calabresi, Chiara Carretta, Simone Romagnoli, Giada Rotunno, Sandra Parenti, Matteo Bertesi, Niccolò Bartalucci, Sebastiano Rontauroli, Chiara Chiereghin, Sara Castellano, Giulia Gentili, Chiara Maccari, Fiorenza Vanderwert, Francesco Mannelli, Matteo Della Porta, Rossella Manfredini, Alessandro Maria Vannucchi, Paola Guglielmelli American Journal of Hematology, 2023
Diagnostic and therapeutic challenges in mast cell sarcoma Francesco Mannelli, Francesca Gesullo, Carmela Mannarelli, Fiorenza Vanderwert, Stefano Lazzi, Francesco Mungai, Valentina Berti, Raffaella Santi, Paola Guglielmelli, Alessandro M. Vannucchi American Journal of Hematology, 2023
Management of polycythemia vera: A survey of treatment patterns in Italy Giuseppe Alberto Palumbo, Massimo Breccia, Claudia Baratè, Massimiliano Bonifacio, Elena Maria Elli, Alessandra Iurlo, Novella Pugliese, Elena Rossi, Paola Guglielmelli, Francesca Palandri European Journal of Haematology, 2023
Disease correlates and clinical relevance of hereditary α-tryptasemia in patients with systemic mastocytosis Benedetta Sordi, Fiorenza Vanderwert, Francesca Crupi, Francesca Gesullo, Roberta Zanotti, Patrizia Bonadonna, Lara Crosera, Chiara Elena, Nicolas Fiorelli, Jacqueline Ferrari, Federica Grifoni, Mariarita Sciumè, Roberta Parente, Massimo Triggiani, Boaz Palterer, Valentina Mecheri, Fabio Almerigogna, Raffaella Santi, Lisa Di Medio, Maria Luisa Brandi, Maria Loredana Iorno, Isabella Ciardetti, Sara Bencini, Francesco Annunziato, Carmela Mannarelli, Lisa Pieri, Paola Guglielmelli, Francesco Mannelli, Alessandro M. Vannucchi Journal of Allergy and Clinical Immunology, 2023
Determinants of early triage for hospitalization in myeloproliferative neoplasm (MPN) patients with COVID-19 Tiziano Barbui, Alessandra Carobbio, Arianna Ghirardi, Alessandra Iurlo, Marta Anna Sobas, Elena Maria Elli, Elisa Rumi, Valerio De Stefano, Francesca Lunghi, Monia Marchetti, Rosa Daffini, Mercedes Gasior Kabat, Beatriz Cuevas, Maria Laura Fox, Marcio Miguel Andrade‐Campos, Francesca Palandri, Paola Guglielmelli, Giulia Benevolo, Claire Harrison, Maria‐Angeles Foncillas, Massimiliano Bonifacio, Alberto Alvarez‐Larran, Jean‐Jacques Kiladjian, Estefanía Bolaños Calderón, Andrea Patriarca, Keina Quiroz Cervantes, Martin Griesshammer, Valentin Garcia‐Gutierrez, Alberto Marin Sanchez, Elena Magro Mazo, Giuseppe Carli, Juan Carlos Hernandez‐Boluda, Santiago Osorio, Gonzalo Carreno‐Tarragona, Miguel Sagues Serrano, Rajko Kusec, Begona Navas Elorza, Anna Angona, Blanca Xicoy Cirici, Emma Lopez Abadia, Steffen Koschmieder, Daniele Cattaneo, Cristina Bucelli, Edyta Cichocka, Anna Kulikowska de Nałęcz, Fabrizio Cavalca, Oscar Borsani, Silvia Betti, Marta Bellini, Natalia Curto‐Garcia, Alessandro Rambaldi, Alessandro Maria Vannucchi American Journal of Hematology, 2022
Increased risk of thrombosis in JAK2 V617F-positive patients with primary myelofibrosis and interaction of the mutation with the IPSS score Tiziano Barbui, Arianna Ghirardi, Alessandra Carobbio, Arianna Masciulli, Greta Carioli, Alessandro Rambaldi, Maria Chiara Finazzi, Marta Bellini, Elisa Rumi, Daniele Vanni, Oscar Borsani, Francesco Passamonti, Barbara Mora, Marco Brociner, Paola Guglielmelli, Chiara Paoli, Alberto Alvarez-Larran, Ana Triguero, Marta Garrote, Helna Pettersson, Björn Andréasson, Giovanni Barosi, Alessandro Maria Vannucchi Blood Cancer Journal, 2022
Breakthrough infections in MPN-COVID vaccinated patients Tiziano Barbui, Alessandra Carobbio, Arianna Ghirardi, Alessandra Iurlo, Valerio De Stefano, Marta Anna Sobas, Elisa Rumi, Elena Maria Elli, Francesca Lunghi, Mercedes Gasior Kabat, Beatriz Cuevas, Paola Guglielmelli, Massimiliano Bonifacio, Monia Marchetti, Alberto Alvarez-Larran, Laura Fox, Marta Bellini, Rosa Daffini, Giulia Benevolo, Gonzalo Carreno-Tarragona, Andrea Patriarca, Haifa Kathrin Al-Ali, Maria Marcio Miguel Andrade-Campos, Francesca Palandri, Claire Harrison, Maria Angeles Foncillas, Santiago Osorio, Steffen Koschmieder, Elena Magro Mazo, Jean-Jacques Kiladjian, Estefanía Bolaños Calderón, Florian H. Heidel, Keina Quiroz Cervantes, Martin Griesshammer, Valentin Garcia-Gutierrez, Alberto Marin Sanchez, Juan Carlos Hernandez-Boluda, Emma Lopez Abadia, Giuseppe Carli, Miguel Sagues Serrano, Rajko Kusec, Blanca Xicoy Cirici, Margarita Guenova, Begona Navas Elorza, Anna Angona, Edyta Cichocka, Anna Kulikowska de Nałęcz, Daniele Cattaneo, Cristina Bucelli, Silvia Betti, Oscar Borsani, Fabrizio Cavalca, Sara Carbonell, Natalia Curto-Garcia, Lina Benajiba, Alessandro Rambaldi, Alessandro Maria Vannucchi Blood Cancer Journal, 2022
Prediction of thrombosis in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study on 1258 patients Barbara Mora, Paola Guglielmelli, Andrew Kuykendall, Elisa Rumi, Margherita Maffioli, Francesca Palandri, Valerio De Stefano, Marianna Caramella, Silvia Salmoiraghi, Jean-Jacques Kiladjian, Jason Gotlib, Alessandra Iurlo, Francisco Cervantes, Marco Ruggeri, Richard T. Silver, Francesco Albano, Giulia Benevolo, David M. Ross, Matteo G. Della Porta, Timothy Devos, Giada Rotunno, Rami S. Komrokji, Ilaria C. Casetti, Michele Merli, Marco Brociner, Domenica Caramazza, Giuseppe Auteri, Tiziano Barbui, Daniele Cattaneo, Lorenza Bertù, Luca Arcaini, Alessandro M. Vannucchi, Francesco Passamonti Leukemia, 2022
Second versus first wave of COVID-19 in patients with MPN Tiziano Barbui, Alessandra Iurlo, Arianna Masciulli, Alessandra Carobbio, Arianna Ghirardi, Greta Carioli, Marta Anna Sobas, Elena Maria Elli, Elisa Rumi, Valerio De Stefano, Francesca Lunghi, Monia Marchetti, Rosa Daffini, Mercedes Gasior Kabat, Beatriz Cuevas, Maria Laura Fox, Marcio Miguel Andrade-Campos, Francesca Palandri, Paola Guglielmelli, Giulia Benevolo, Claire Harrison, Maria Angeles Foncillas, Massimiliano Bonifacio, Alberto Alvarez-Larran, Jean-Jacques Kiladjian, Estefanía Bolaños Calderón, Andrea Patriarca, Keina Quiroz Cervantes, Martin Griessammer, Valentin Garcia-Gutierrez, Alberto Marin Sanchez, Elena Magro Mazo, Marco Ruggeri, Juan Carlos Hernandez-Boluda, Santiago Osorio, Gonzalo Carreno-Tarragona, Miguel Sagues Serrano, Rajko Kusec, Begona Navas Elorza, Anna Angona, Blanca Xicoy Cirici, Emma Lopez Abadia, Steffen Koschmieder, Daniele Cattaneo, Cristina Bucelli, Edyta Cichocka, Anna Masternak Kulikowska de Nałęcz, Fabrizio Cavalca, Oscar Borsani, Silvia Betti, Lina Benajiba, Marta Bellini, Natalia Curto-Garcia, Alessandro Rambaldi, Alessandro Maria Vannucchi Leukemia, 2022
Impact of ruxolitinib on survival of patients with myelofibrosis in the real world: Update of the ERNEST Study Paola Guglielmelli, Arianna Ghirardi, Alessandra Carobbio, Arianna Masciulli, Chiara Maccari, Barbara Mora, Elisa Rumi, Ana Triguero, Maria Chiara Finazzi, Helna Pettersson, Chiara Paoli, Francesco Mannelli, Daniele Vanni, Alessandro Rambaldi, Francesco Passamonti, Alberto Alvarez-Larràn, Bjorn Andreasson, Alessandro M. Vannucchi, Tiziano Barbui Blood Advances, 2022
The Response to Oxidative Damage Correlates with Driver Mutations and Clinical Outcome in Patients with Myelofibrosis Elena Genovese, Margherita Mirabile, Sebastiano Rontauroli, Stefano Sartini, Sebastian Fantini, Lara Tavernari, Monica Maccaferri, Paola Guglielmelli, Elisa Bianchi, Sandra Parenti, Chiara Carretta, Selene Mallia, Sara Castellano, Corrado Colasante, Manjola Balliu, Niccolò Bartalucci, Raffaele Palmieri, Tiziana Ottone, Barbara Mora, Leonardo Potenza, Francesco Passamonti, Maria Teresa Voso, Mario Luppi, Alessandro Maria Vannucchi, Enrico Tagliafico, Rossella Manfredini, and Antioxidants, 2022
Long-term follow-up of recovered MPN patients with COVID-19 Tiziano Barbui, Alessandra Iurlo, Arianna Masciulli, Alessandra Carobbio, Arianna Ghirardi, Giuseppe Rossi, Claire Harrison, Alberto Alvarez-Larran, Elena Maria Elli, Jean-Jaques Kiladjian, Mercedes Gasior Kabat, Alberto Marin Sanchez, Francesca Palandri, Marcio Miguel Andrade-Campos, Alessandro Maria Vannucchi, Gonzalo Carreno-Tarragona, Petros Papadopoulos, Keina Quiroz Cervantes, Maria Angeles Foncillas, Maria Laura Fox, Miguel Sagues Serrano, Elisa Rumi, Santiago Osorio, Giulia Benevolo, Andrea Patriarca, Begona Navas Elorza, Valentin Garcia-Gutierrez, Elena Magro Mazo, Francesca Lunghi, Massimiliano Bonifacio, Valerio De Stefano, Juan Carlos Hernandez-Boluda, Emma Lopez Abadia, Anna Angona, Blanca Xicoy Cirici, Marco Ruggeri, Steffen Koschmieder, Marta Anna Sobas, Beatriz Cuevas, Daniele Cattaneo, Rosa Daffini, Marta Bellini, Natalia Curto-Garcia, Marta Garrote, Fabrizio Cavalca, Lina Benajiba, Beatriz Bellosillo, Paola Guglielmelli, Oscar Borsani, Silvia Betti, Silvia Salmoiraghi, Alessandro Rambaldi Blood Cancer Journal, 2021
Mutations and thrombosis in essential thrombocythemia Paola Guglielmelli, Naseema Gangat, Giacomo Coltro, Terra L. Lasho, Giuseppe Gaetano Loscocco, Christy M. Finke, Erika Morsia, Benedetta Sordi, Natasha Szuber, Curtis A. Hanson, Animesh Pardanani, Alessandro M. Vannucchi, Ayalew Tefferi Blood Cancer Journal, 2021
Compassionate use of JAK1/2 inhibitor ruxolitinib for severe COVID-19: a prospective observational study Alessandro M. Vannucchi, Benedetta Sordi, Alessandro Morettini, Carlo Nozzoli, Loredana Poggesi, Filippo Pieralli, Alessandro Bartoloni, Alessandro Atanasio, Filippo Miselli, Chiara Paoli, Giuseppe G. Loscocco, Andrea Fanelli, Ombretta Para, Andrea Berni, Irene Tassinari, Lorenzo Zammarchi, Laura Maggi, Alessio Mazzoni, Valentina Scotti, Giorgia Falchetti, Danilo Malandrino, Fabio Luise, Giovanni Millotti, Sara Bencini, Manuela Capone, Marie Pierre Piccinni, Francesco Annunziato, Paola Guglielmelli, Francesco Mannelli, Giacomo Coltro, Duccio Fantoni, Miriam Borella, Enrica Ravenda, Benedetta Peruzzi, Roberto Caporale, Lorenzo Cosmi, Francesco Liotta, Letizia Lombardelli, Federica Logiodice, Anna Vanni, Lorenzo Salvati, Chiara Lazzeri, Manuela Bonizzoli, Adriano Peris, Giovanni Cianchi, Alberto Bosi, Michela Pucatti, Paolo Fontanari, Silvia Benemei, Marco Matucci Cerinic, Lucia Turco, and Leukemia, 2021
Gene expression profile correlates with molecular and clinical features in patients with myelofibrosis Sebastiano Rontauroli, Sara Castellano, Paola Guglielmelli, Roberta Zini, Elisa Bianchi, Elena Genovese, Chiara Carretta, Sandra Parenti, Sebastian Fantini, Selene Mallia, Lara Tavernari, Stefano Sartini, Margherita Mirabile, Carmela Mannarelli, Francesca Gesullo, Annalisa Pacilli, Daniela Pietra, Elisa Rumi, Silvia Salmoiraghi, Barbara Mora, Laura Villani, Andrea Grilli, Vittorio Rosti, Giovanni Barosi, Francesco Passamonti, Alessandro Rambaldi, Luca Malcovati, Mario Cazzola, Silvio Bicciato, Enrico Tagliafico, Alessandro M. Vannucchi, Rossella Manfredini Blood Advances, 2021
Ropeginterferon alfa-2b versus phlebotomy in low-risk patients with polycythaemia vera (Low-PV study): a multicentre, randomised phase 2 trial Tiziano Barbui, Alessandro Maria Vannucchi, Valerio De Stefano, Arianna Masciulli, Alessandra Carobbio, Alberto Ferrari, Arianna Ghirardi, Elena Rossi, Fabio Ciceri, Massimiliano Bonifacio, Alessandra Iurlo, Francesca Palandri, Giulia Benevolo, Fabrizio Pane, Alessandra Ricco, Giuseppe Carli, Marianna Caramella, Davide Rapezzi, Caterina Musolino, Sergio Siragusa, Elisa Rumi, Andrea Patriarca, Nicola Cascavilla, Barbara Mora, Emma Cacciola, Carmela Mannarelli, Giuseppe Gaetano Loscocco, Paola Guglielmelli, Silvia Betti, Francesca Lunghi, Luigi Scaffidi, Cristina Bucelli, Nicola Vianelli, Marta Bellini, Maria Chiara Finazzi, Gianni Tognoni, Alessandro Rambaldi Lancet Haematology, 2021
Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis Gabriella Galatà, Andrés C. García-Montero, Thomas Kristensen, Ahmed A.Z. Dawoud, Javier I. Muñoz-González, Manja Meggendorfer, Paola Guglielmelli, Yvette Hoade, Ivan Alvarez-Twose, Christian Gieger, Konstantin Strauch, Luigi Ferrucci, Toshiko Tanaka, Stefania Bandinelli, Theresia M. Schnurr, Torsten Haferlach, Sigurd Broesby-Olsen, Hanne Vestergaard, Michael Boe Møller, Carsten Bindslev-Jensen, Alessandro M. Vannucchi, Alberto Orfao, Deepti Radia, Andreas Reiter, Andrew J. Chase, Nicholas C.P. Cross, William J. Tapper American Journal of Human Genetics, 2021
Among classic myeloproliferative neoplasms, essential thrombocythemia is associated with the greatest risk of venous thromboembolism during COVID-19 Tiziano Barbui, Valerio De Stefano, Alberto Alvarez-Larran, Alessandra Iurlo, Arianna Masciulli, Alessandra Carobbio, Arianna Ghirardi, Alberto Ferrari, Valeria Cancelli, Elena Maria Elli, Marcio Miguel Andrade-Campos, Mercedes Gasior Kabat, Jean-Jaques Kiladjian, Francesca Palandri, Giulia Benevolo, Valentin Garcia-Gutierrez, Maria Laura Fox, Maria Angeles Foncillas, Carmen Montoya Morcillo, Elisa Rumi, Santiago Osorio, Petros Papadopoulos, Massimiliano Bonifacio, Keina Susana Quiroz Cervantes, Miguel Sagues Serrano, Gonzalo Carreno-Tarragona, Marta Anna Sobas, Francesca Lunghi, Andrea Patriarca, Begoña Navas Elorza, Anna Angona, Elena Magro Mazo, Steffen Koschmieder, Giuseppe Carli, Beatriz Cuevas, Juan Carlos Hernandez-Boluda, Emma Lopez Abadia, Blanca Xicoy Cirici, Paola Guglielmelli, Marta Garrote, Daniele Cattaneo, Rosa Daffini, Fabrizio Cavalca, Beatriz Bellosillo, Lina Benajiba, Natalia Curto-Garcia, Marta Bellini, Silvia Betti, Claire Harrison, Alessandro Rambaldi, Alessandro Maria Vannucchi Blood Cancer Journal, 2021
High mortality rate in COVID-19 patients with myeloproliferative neoplasms after abrupt withdrawal of ruxolitinib Tiziano Barbui, Alessandro Maria Vannucchi, Alberto Alvarez-Larran, Alessandra Iurlo, Arianna Masciulli, Alessandra Carobbio, Arianna Ghirardi, Alberto Ferrari, Giuseppe Rossi, Elena Elli, Marcio Miguel Andrade-Campos, Mercedes Gasior Kabat, Jean-Jaques Kiladjian, Francesca Palandri, Giulia Benevolo, Valentin Garcia-Gutierrez, Maria Laura Fox, Maria Angeles Foncillas, Carmen Montoya Morcillo, Elisa Rumi, Santiago Osorio, Petros Papadopoulos, Massimiliano Bonifacio, Keina Susana Quiroz Cervantes, Miguel Sagues Serrano, Gonzalo Carreno-Tarragona, Marta Anna Sobas, Francesca Lunghi, Andrea Patriarca, Begona Navas Elorza, Anna Angona, Elena Magro Mazo, Steffen Koschmieder, Marco Ruggeri, Beatriz Cuevas, Juan Carlos Hernandez-Boluda, Emma Lopez Abadia, Blanca Xicoy Cirici, Paola Guglielmelli, Marta Garrote, Daniele Cattaneo, Rosa Daffini, Fabrizio Cavalca, Beatriz Bellosillo, Lina Benajiba, Natalia Curto-Garcia, Marta Bellini, Silvia Betti, Valerio De Stefano, Claire Harrison, Alessandro Rambaldi Leukemia, 2021
The MPL mutation Paola Guglielmelli, Laura Calabresi International Review of Cell and Molecular Biology, 2021
Genetic lesions disrupting calreticulin 3′-untranslated region in JAK2 mutation-negative polycythemia vera Alberto Quattrocchi, Carlo Maiorca, Monia Billi, Simona Tomassini, Elisabetta De Marinis, Natalia Cenfra, Francesco Equitani, Martina Gentile, Alessia Ceccherelli, Cristina Banella, Sergio Mecarocci, Maria Cristina Scerpa, Stefania Pisanò, Annalisa Pacilli, Claudio Di Cristofano, Massimiliano Mancini, Paola Guglielmelli, Alessandro Maria Vannucchi, Nelida Noguera, Francesco Grignani, Giuseppe Cimino, Clara Nervi American Journal of Hematology, 2020
A randomized double-blind trial of 3 aspirin regimens to optimize antiplatelet therapy in essential thrombocythemia Bianca Rocca, Alberto Tosetto, Silvia Betti, Denise Soldati, Giovanna Petrucci, Elena Rossi, Andrea Timillero, Viviana Cavalca, Benedetta Porro, Alessandra Iurlo, Daniele Cattaneo, Cristina Bucelli, Alfredo Dragani, Mauro Di Ianni, Paola Ranalli, Francesca Palandri, Nicola Vianelli, Eloise Beggiato, Giuseppe Lanzarone, Marco Ruggeri, Giuseppe Carli, Elena Maria Elli, Monica Carpenedo, Maria Luigia Randi, Irene Bertozzi, Chiara Paoli, Giorgina Specchia, Alessandra Ricco, Alessandro Maria Vannucchi, Francesco Rodeghiero, Carlo Patrono, Valerio De Stefano Blood, 2020
Second cancers in MPN: Survival analysis from an international study Monia Marchetti, Arianna Ghirardi, Arianna Masciulli, Alessandra Carobbio, Francesca Palandri, Nicola Vianelli, Elena Rossi, Silvia Betti, Ambra Di Veroli, Alessandra Iurlo, Daniele Cattaneo, Guido Finazzi, Massimiliano Bonifacio, Luigi Scaffidi, Andrea Patriarca, Elisa Rumi, Ilaria Carola Casetti, Clemency Stephenson, Paola Guglielmelli, Elena Maria Elli, Miroslava Palova, Davide Rapezzi, Daniel Erez, Montse Gomez, Kai Wille, Manuel Perez‐Encinas, Francesca Lunghi, Anna Angona, Maria Laura Fox, Eloise Beggiato, Giulia Benevolo, Giuseppe Carli, Rossella Cacciola, Mary Frances McMullin, Alessia Tieghi, Valle Recasens, Susanne Isfort, Fabrizio Pane, Valerio De Stefano, Martin Griesshammer, Alberto Alvarez‐Larran, Alessandro Maria Vannucchi, Alessandro Rambaldi, Tiziano Barbui American Journal of Hematology, 2020
Validation of the IPSET score for thrombosis in patients with prefibrotic myelofibrosis Paola Guglielmelli, Alessandra Carobbio, Elisa Rumi, Valerio De Stefano, Lara Mannelli, Francesco Mannelli, Giada Rotunno, Giacomo Coltro, Silvia Betti, Chiara Cavalloni, Maria Chiara Finazzi, Juergen Thiele, Mario Cazzola, Alessandro Maria Vannucchi, Tiziano Barbui Blood Cancer Journal, 2020
Splanchnic vein thromboses associated with myeloproliferative neoplasms: An international, retrospective study on 518 cases Emanuela Sant'Antonio, Paola Guglielmelli, Lisa Pieri, Massimo Primignani, Maria Luigia Randi, Claudia Santarossa, Elisa Rumi, Francisco Cervantes, Federica Delaini, Alessandra Carobbio, Silvia Betti, Elena Rossi, Noa Lavi, Claire N. Harrison, Natalia Curto‐Garcia, Heinz Gisslinger, Bettina Gisslinger, Giorgina Specchia, Alessandra Ricco, Nicola Vianelli, Nicola Polverelli, Maya Koren‐Michowitz, Marco Ruggeri, Francois Girodon, Martin Ellis, Alessandra Iurlo, Francesco Mannelli, Lara Mannelli, Benedetta Sordi, Giuseppe Gaetano Loscocco, Mario Cazzola, Valerio De Stefano, Tiziano Barbui, Ayalew Tefferi, Alessandro Maria Vannucchi American Journal of Hematology, 2020
Arterial thrombosis in Philadelphia-negative myeloproliferative neoplasms predicts second cancer: A case-control study Valerio De Stefano, Arianna Ghirardi, Arianna Masciulli, Alessandra Carobbio, Francesca Palandri, Nicola Vianelli, Elena Rossi, Silvia Betti, Ambra Di Veroli, Alessandra Iurlo, Daniele Cattaneo, Guido Finazzi, Massimiliano Bonifacio, Luigi Scaffidi, Andrea Patriarca, Elisa Rumi, Ilaria Carola Casetti, Clemency Stephenson, Paola Guglielmelli, Elena Maria Elli, Miroslava Palova, Davide Rapezzi, Daniel Erez, Montse Gomez, Kai Wille, Manuel Perez-Encinas, Francesca Lunghi, Anna Angona, Maria Laura Fox, Eloise Beggiato, Giulia Benevolo, Giuseppe Carli, Rossella Cacciola, Mary Frances McMullin, Alessia Tieghi, Valle Recasens, Susanne Isfort, Monia Marchetti, Martin Griesshammer, Alberto Alvarez-Larran, Alessandro Maria Vannucchi, Alessandro Rambaldi, Tiziano Barbui Blood, 2020
Impact of bone marrow fibrosis grade in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: A study of the MYSEC group Barbara Mora, Paola Guglielmelli, Elisa Rumi, Margherita Maffioli, Daniela Barraco, Alessandro Rambaldi, Marianna Caramella, Rami S. Komrokji, Jean‐Jacques Kiladjian, Jason Gotlib, Alessandra Iurlo, Francisco Cervantes, Timothy Devos, Francesca Palandri, Valerio De Stefano, Marco Ruggeri, Richard T. Silver, Francesco Albano, Giulia Benevolo, Chiara Cavalloni, Silvia Uccella, Raffaella Accetta, Claudia Siracusa, Stefania Agnoli, Michele Merli, Tiziano Barbui, Lorenza Bertù, Mario Cazzola, Alessandro M. Vannucchi, Francesco Passamonti American Journal of Hematology, 2020
Italian survey on clinical practice in myeloproliferative neoplasms. A GIMEMA Myeloproliferative Neoplasms Working Party initiative Giuseppe G. Loscocco, Francesco Mannelli, Paola Guglielmelli, Chiara Paoli, Ilaria Marone, Rosalba Cucci, Giacomo Coltro, Benedetta Sordi, Francesco Albano, Massimo Breccia, Valerio De Stefano, Guido Finazzi, Alessandra Iurlo, Bruno Martino, Francesca Palandri, Francesco Passamonti, Sergio Siragusa, Lara Mannelli, Duccio Fantoni, Paola Fazi, Sergio Amadori, Marco Vignetti, Tiziano Barbui, Alessandro M. Vannucchi American Journal of Hematology, 2019
Second cancer in Philadelphia negative myeloproliferative neoplasms (MPN-K). A nested case-control study Tiziano Barbui, Arianna Ghirardi, Arianna Masciulli, Alessandra Carobbio, Francesca Palandri, Nicola Vianelli, Valerio De Stefano, Silvia Betti, Ambra Di Veroli, Alessandra Iurlo, Daniele Cattaneo, Federica Delaini, Massimiliano Bonifacio, Luigi Scaffidi, Andrea Patriarca, Elisa Rumi, Ilaria Carola Casetti, Clemency Stephenson, Paola Guglielmelli, Elena Maria Elli, Miroslava Palova, Laura Bertolotti, Daniel Erez, Montse Gomez, Kai Wille, Manuel Perez-Encinas, Francesca Lunghi, Anna Angona, Maria Laura Fox, Eloise Beggiato, Giulia Benevolo, Giuseppe Carli, Rossella Cacciola, Mary Frances McMullin, Alessia Tieghi, Valle Recasens, Monia Marchetti, Martin Griesshammer, Alberto Alvarez-Larran, Alessandro Maria Vannucchi, Guido Finazzi Leukemia, 2019
Circ RNAs are here to stay: A perspective on the MLL recombinome Anna Dal Molin, Silvia Bresolin, Enrico Gaffo, Caterina Tretti, Elena Boldrin, Lueder H. Meyer, Paola Guglielmelli, Alessandro M. Vannucchi, Geertruij te Kronnie, Stefania Bortoluzzi Frontiers in Genetics, 2019
Second primary malignancies in postpolycythemia vera and postessential thrombocythemia myelofibrosis: A study on 2233 patients Barbara Mora, Elisa Rumi, Paola Guglielmelli, Daniela Barraco, Margherita Maffioli, Alessandro Rambaldi, Marianna Caramella, Rami Komrokji, Jason Gotlib, Jean Jacques Kiladjian, Francisco Cervantes, Timothy Devos, Francesca Palandri, Valerio De Stefano, Marco Ruggeri, Richard T. Silver, Giulia Benevolo, Francesco Albano, Chiara Cavalloni, Daniela Pietra, Tiziano Barbui, Giada Rotunno, Mario Cazzola, Alessandro Maria Vannucchi, Toni Giorgino, Francesco Passamonti Cancer Medicine, 2019
Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea Annalisa Pacilli, Giada Rotunno, Carmela Mannarelli, Tiziana Fanelli, Alessandro Pancrazzi, Elisa Contini, Francesco Mannelli, Francesca Gesullo, Niccolò Bartalucci, Giuditta Corbizi Fattori, Chiara Paoli, Alessandro M. Vannucchi, Paola Guglielmelli Blood Cancer Journal, 2018
Role of TGF-β1/miR-382-5p/SOD2 axis in the induction of oxidative stress in CD34+ cells from primary myelofibrosis Chiara Rossi, Roberta Zini, Sebastiano Rontauroli, Samantha Ruberti, Zelia Prudente, Greta Barbieri, Elisa Bianchi, Simona Salati, Elena Genovese, Niccolò Bartalucci, Paola Guglielmelli, Enrico Tagliafico, Vittorio Rosti, Giovanni Barosi, Alessandro M. Vannucchi, Rossella Manfredini, the AGIMM (AIRC‐Gruppo Italiano Malattie Mieloproliferative) investigators Molecular Oncology, 2018
Classification and personalized prognosis in myeloproliferative neoplasms Jacob Grinfeld, Jyoti Nangalia, E. Joanna Baxter, David C. Wedge, Nicos Angelopoulos, Robert Cantrill, Anna L. Godfrey, Elli Papaemmanuil, Gunes Gundem, Cathy MacLean, Julia Cook, Laura O’Neil, Sarah O’Meara, Jon W. Teague, Adam P. Butler, Charlie E. Massie, Nicholas Williams, Francesca L. Nice, Christen L. Andersen, Hans C. Hasselbalch, Paola Guglielmelli, Mary F. McMullin, Alessandro M. Vannucchi, Claire N. Harrison, Moritz Gerstung, Anthony R. Green, Peter J. Campbell New England Journal of Medicine, 2018
Gender effect on phenotype and genotype in patients with post-polycythemia vera and post-essential thrombocythemia myelofibrosis: results from the MYSEC project Daniela Barraco, Barbara Mora, Paola Guglielmelli, Elisa Rumi, Margherita Maffioli, Alessandro Rambaldi, Marianna Caramella, Rami Komrokji, Jason Gotlib, Jean Jacques Kiladjian, Francisco Cervantes, Timothy Devos, Francesca Palandri, Valerio De Stefano, Marco Ruggeri, Richard T. Silver, Giulia Benevolo, Francesco Albano, Michele Merli, Daniela Pietra, Tiziano Barbui, Giada Rotunno, Mario Cazzola, Toni Giorgino, Alessandro Maria Vannucchi, Francesco Passamonti Blood Cancer Journal, 2018
Value of cytogenetic abnormalities in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: A study of the MYSEC project Barbara Mora, Toni Giorgino, Paola Guglielmelli, Elisa Rumi, Margherita Maffioli, Alessandro Rambaldi, Marianna Caramella, Rami Komrokji, Jason Gotlib, Jean Jacques Kiladjian, Francisco Cervantes, Timothy Devos, Francesca Palandri, Valerio De Stefano, Marco Ruggeri, Richard T. Silver, Giulia Benevolo, Francesco Albano, Chiara Cavalloni, Daniela Barraco, Michele Merli, Daniela Pietra, Rosario Casalone, Tiziano Barbui, Giada Rotunno, Mario Cazzola, Alessandro Maria Vannucchi, Francesco Passamonti Haematologica, 2018
GIPSS: Genetically inspired prognostic scoring system for primary myelofibrosis Ayalew Tefferi, Paola Guglielmelli, Maura Nicolosi, Francesco Mannelli, Mythri Mudireddy, Niccolo Bartalucci, Christy M. Finke, Terra L. Lasho, Curtis A. Hanson, Rhett P. Ketterling, Kebede H. Begna, Naseema Gangat, Animesh Pardanani, Alessandro M. Vannucchi Leukemia, 2018
Blast phase myeloproliferative neoplasm: Mayo-AGIMM study of 410 patients from two separate cohorts Ayalew Tefferi, Mythri Mudireddy, Francesco Mannelli, Kebede H. Begna, Mrinal M. Patnaik, Curtis A. Hanson, Rhett P. Ketterling, Naseema Gangat, Meera Yogarajah, Valerio De Stefano, Francesco Passamonti, Vittorio Rosti, Maria Chiara Finazzi, Alessandro Rambaldi, Alberto Bosi, Paola Guglielmelli, Animesh Pardanani, Alessandro M. Vannucchi Leukemia, 2018
The spleen of patients with myelofibrosis harbors defective mesenchymal stromal cells Maria Antonietta Avanzini, Vittorio Abbonante, Paolo Catarsi, Irene Dambruoso, Melissa Mantelli, Valentina Poletto, Elisa Lenta, Paola Guglielmelli, Stefania Croce, Lorenzo Cobianchi, Basilio Jemos, Rita Campanelli, Elisa Bonetti, Christian Andrea Di Buduo, Silvia Salmoiraghi, Laura Villani, Margherita Massa, Marina Boni, Rita Zappatore, Alessandra Iurlo, Alessandro Rambaldi, Alessandro Maria Vannucchi, Paolo Bernasconi, Alessandra Balduini, Giovanni Barosi, Vittorio Rosti, on behalf of the AGIMM Investigators American Journal of Hematology, 2018
Benefit-risk profile of cytoreductive drugs along with antiplatelet and antithrombotic therapy after transient ischemic attack or ischemic stroke in myeloproliferative neoplasms Valerio De Stefano, Alessandra Carobbio, Vincenzo Di Lazzaro, Paola Guglielmelli, Alessandra Iurlo, Maria Chiara Finazzi, Elisa Rumi, Francisco Cervantes, Elena Maria Elli, Maria Luigia Randi, Martin Griesshammer, Francesca Palandri, Massimiliano Bonifacio, Juan-Carlos Hernandez-Boluda, Rossella Cacciola, Palova Miroslava, Giuseppe Carli, Eloise Beggiato, Martin H. Ellis, Caterina Musolino, Gianluca Gaidano, Davide Rapezzi, Alessia Tieghi, Francesca Lunghi, Giuseppe Gaetano Loscocco, Daniele Cattaneo, Agostino Cortelezzi, Silvia Betti, Elena Rossi, Guido Finazzi, Bruno Censori, Mario Cazzola, Marta Bellini, Eduardo Arellano-Rodrigo, Irene Bertozzi, Parvis Sadjadian, Nicola Vianelli, Luigi Scaffidi, Montse Gomez, Emma Cacciola, Alessandro M. Vannucchi, Tiziano Barbui Blood Cancer Journal, 2018
MIPSS70: Mutation-enhanced international prognostic score system for transplantation-age patients with primary myelofibrosis Paola Guglielmelli, Terra L. Lasho, Giada Rotunno, Mythri Mudireddy, Carmela Mannarelli, Maura Nicolosi, Annalisa Pacilli, Animesh Pardanani, Elisa Rumi, Vittorio Rosti, Curtis A. Hanson, Francesco Mannelli, Rhett P. Ketterling, Naseema Gangat, Alessandro Rambaldi, Francesco Passamonti, Giovanni Barosi, Tiziano Barbui, Mario Cazzola, Alessandro M. Vannucchi, Ayalew Tefferi Journal of Clinical Oncology, 2018
Involvement of MAF/SPP1 axis in the development of bone marrow fibrosis in PMF patients , S Ruberti, E Bianchi, P Guglielmelli, S Rontauroli, G Barbieri, L Tavernari, T Fanelli, R Norfo, V Pennucci, G Corbizi Fattori, C Mannarelli, N Bartalucci, B Mora, L Elli, M A Avanzini, C Rossi, S Salmoiraghi, R Zini, S Salati, Z Prudente, V Rosti, F Passamonti, A Rambaldi, S Ferrari, E Tagliafico, A M Vannucchi, R Manfredini Leukemia, 2018
Splanchnic vein thrombosis in myeloproliferative neoplasms: Risk factors for recurrences in a cohort of 181 patients V De Stefano, A M Vannucchi, M Ruggeri, F Cervantes, A Alvarez-Larrán, A Iurlo, M L Randi, L Pieri, E Rossi, P Guglielmelli, S Betti, E Elli, M C Finazzi, G Finazzi, E Zetterberg, N Vianelli, G Gaidano, I Nichele, D Cattaneo, M Palova, M H Ellis, E Cacciola, A Tieghi, J C Hernandez-Boluda, E Pungolino, G Specchia, D Rapezzi, A Forcina, C Musolino, A Carobbio, M Griesshammer, T Barbui Blood Cancer Journal, 2016
Prognostic impact of bone marrow fibrosis in primary myelofibrosis. A study of the AGIMM group on 490 patients Paola Guglielmelli, Giada Rotunno, Annalisa Pacilli, Elisa Rumi, Vittorio Rosti, Federica Delaini, Margherita Maffioli, Tiziana Fanelli, Alessandro Pancrazzi, Lisa Pieri, Rajmonda Fjerza, Daniela Pietra, Daniela Cilloni, Emanuela Sant'Antonio, Silvia Salmoiraghi, Francesco Passamonti, Alessandro Rambaldi, Giovanni Barosi, Tiziano Barbui, Mario Cazzola, Alessandro M. Vannucchi American Journal of Hematology, 2016
Antiplatelet therapy versus observation in low-risk essential thrombocythemia with a CALR mutation A. Alvarez-Larran, A. Pereira, P. Guglielmelli, J. C. Hernandez-Boluda, E. Arellano-Rodrigo, F. Ferrer-Marin, A. Samah, M. Griesshammer, A. Kerguelen, B. Andreasson, C. Burgaleta, J. Schwarz, V. Garcia-Gutierrez, R. Ayala, P. Barba, M. T. Gomez-Casares, C. Paoli, B. Drexler, S. Zweegman, M. F. McMullin, J. Samuelsson, C. Harrison, F. Cervantes, A. M. Vannucchi, C. Besses Haematologica, 2016
Ruxolitinib is an effective treatment for CALR-positive patients with myelofibrosis Paola Guglielmelli, Giada Rotunno, Costanza Bogani, Carmela Mannarelli, Laura Giunti, Aldesia Provenzano, Sabrina Giglio, Matthew Squires, Viktoriya Stalbovskaya, Prashanth Gopalakrishna, Alessandro M. Vannucchi, the COMFORT‐II Investigators British Journal of Haematology, 2016
Tie2 expressing monocytes in the spleen of patients with primary myelofibrosis Rita Campanelli, Gabriela Fois, Paolo Catarsi, Valentina Poletto, Laura Villani, Benedetta Gaia Erba, Luigi Maddaluno, Basilio Jemos, Silvia Salmoiraghi, Paola Guglielmelli, Vittorio Abbonante, Christian Andrea Di Buduo, Alessandra Balduini, Alessandra Iurlo, Giovanni Barosi, Vittorio Rosti, Margherita Massa, AGIMM Investigators Plos One, 2016
Integrative analysis of copy number and gene expression data suggests novel pathogenetic mechanisms in primary myelofibrosis Simona Salati, Roberta Zini, Simona Nuzzo, Paola Guglielmelli, Valentina Pennucci, Zelia Prudente, Samantha Ruberti, Sebastiano Rontauroli, Ruggiero Norfo, Elisa Bianchi, Costanza Bogani, Giada Rotunno, Tiziana Fanelli, Carmela Mannarelli, Vittorio Rosti, Silvia Salmoiraghi, Daniela Pietra, Sergio Ferrari, Giovanni Barosi, Alessandro Rambaldi, Mario Cazzola, Silvio Bicciato, Enrico Tagliafico, Alessandro M. Vannucchi, Rossella Manfredini, and International Journal of Cancer, 2016
STAT1 activation in association with JAK2 exon 12 mutations A. L. Godfrey, E. Chen, C. E. Massie, Y. Silber, F. Pagano, B. Bellosillo, P. Guglielmelli, C. N. Harrison, J. T. Reilly, F. Stegelmann, F. Bijou, E. Lippert, J.-M. Boiron, K. Dohner, A. M. Vannucchi, C. Besses, A. R. Green Haematologica, 2016
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms William Tapper, Amy V. Jones, Robert Kralovics, Ashot S. Harutyunyan, Katerina Zoi, William Leung, Anna L. Godfrey, Paola Guglielmelli, Alison Callaway, Daniel Ward, Paula Aranaz, Helen E. White, Katherine Waghorn, Feng Lin, Andrew Chase, E. Joanna Baxter, Cathy Maclean, Jyoti Nangalia, Edwin Chen, Paul Evans, Michael Short, Andrew Jack, Louise Wallis, David Oscier, Andrew S. Duncombe, Anna Schuh, Adam J. Mead, Michael Griffiths, Joanne Ewing, Rosemary E. Gale, Susanne Schnittger, Torsten Haferlach, Frank Stegelmann, Konstanze Döhner, Harald Grallert, Konstantin Strauch, Toshiko Tanaka, Stefania Bandinelli, Andreas Giannopoulos, Lisa Pieri, Carmela Mannarelli, Heinz Gisslinger, Giovanni Barosi, Mario Cazzola, Andreas Reiter, Claire Harrison, Peter Campbell, Anthony R. Green, Alessandro Vannucchi, Nicholas C.P. Cross Nature Communications, 2015
Effect of mutation order on myeloproliferative neoplasms Christina A. Ortmann, David G. Kent, Jyoti Nangalia, Yvonne Silber, David C. Wedge, Jacob Grinfeld, E. Joanna Baxter, Charles E. Massie, Elli Papaemmanuil, Suraj Menon, Anna L. Godfrey, Danai Dimitropoulou, Paola Guglielmelli, Beatriz Bellosillo, Carles Besses, Konstanze Döhner, Claire N. Harrison, George S. Vassiliou, Alessandro Vannucchi, Peter J. Campbell, Anthony R. Green New England Journal of Medicine, 2015
miRNA-mRNA integrative analysis in primary myelofibrosis CD34+cells: Role of miR-155/JARID2 axis in abnormal megakaryopoiesis Ruggiero Norfo, Roberta Zini, Valentina Pennucci, Elisa Bianchi, Simona Salati, Paola Guglielmelli, Costanza Bogani, Tiziana Fanelli, Carmela Mannarelli, Vittorio Rosti, Daniela Pietra, Silvia Salmoiraghi, Andrea Bisognin, Samantha Ruberti, Sebastiano Rontauroli, Giorgia Sacchi, Zelia Prudente, Giovanni Barosi, Mario Cazzola, Alessandro Rambaldi, Stefania Bortoluzzi, Sergio Ferrari, Enrico Tagliafico, Alessandro M. Vannucchi, Rossella Manfredini Blood, 2014
Clinical effect of driver mutations of JAK2, CALR, or MPL in primary myelofibrosis Elisa Rumi, Daniela Pietra, Cristiana Pascutto, Paola Guglielmelli, Alejandra Martínez-Trillos, Ilaria Casetti, Dolors Colomer, Lisa Pieri, Marta Pratcorona, Giada Rotunno, Emanuela Sant’Antonio, Marta Bellini, Chiara Cavalloni, Carmela Mannarelli, Chiara Milanesi, Emanuela Boveri, Virginia Ferretti, Cesare Astori, Vittorio Rosti, Francisco Cervantes, Giovanni Barosi, Alessandro M. Vannucchi, Mario Cazzola Blood, 2014
Essential Thrombocytosis Paola Guglielmelli, Alessandro M. Vannucchi Cancer Consult Expertise for Clinical Practice, 2014
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study Paola Guglielmelli, Flavia Biamonte, Giada Rotunno, Valentina Artusi, Lucia Artuso, Isabella Bernardis, Elena Tenedini, Lisa Pieri, Chiara Paoli, Carmela Mannarelli, Rajmonda Fjerza, Elisa Rumi, Viktoriya Stalbovskaya, Matthew Squires, Mario Cazzola, Rossella Manfredini, Claire Harrison, Enrico Tagliafico, Alessandro M. Vannucchi Blood, 2014
Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients Ayalew Tefferi, Emnet A. Wassie, Paola Guglielmelli, Naseema Gangat, Alem A. Belachew, Terra L. Lasho, Christy Finke, Rhett P. Ketterling, Curtis A. Hanson, Animesh Pardanani, Alexandra P. Wolanskyj, Margherita Maffioli, Rosario Casalone, Annalisa Pacilli, Alessandro M. Vannucchi, Francesco Passamonti American Journal of Hematology, 2014
Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms on behalf of AGIMM investigators, E Tenedini, I Bernardis, V Artusi, L Artuso, E Roncaglia, P Guglielmelli, L Pieri, C Bogani, F Biamonte, G Rotunno, C Mannarelli, E Bianchi, A Pancrazzi, T Fanelli, G Malagoli Tagliazucchi, S Ferrari, R Manfredini, A M Vannucchi, E Tagliafico Leukemia, 2014
Complex Patterns of Chromosome 11 Aberrations in Myeloid Malignancies Target CBL, MLL, DDB1 and LMO2 Thorsten Klampfl, Jelena D. Milosevic, Ana Puda, Andreas Schönegger, Klaudia Bagienski, Tiina Berg, Ashot S. Harutyunyan, Bettina Gisslinger, Elisa Rumi, Luca Malcovati, Daniela Pietra, Chiara Elena, Matteo Giovanni Della Porta, Lisa Pieri, Paola Guglielmelli, Christoph Bock, Michael Doubek, Dana Dvorakova, Nada Suvajdzic, Dragica Tomin, Natasa Tosic, Zdenek Racil, Michael Steurer, Sonja Pavlovic, Alessandro M. Vannucchi, Mario Cazzola, Heinz Gisslinger, Robert Kralovics Plos One, 2013
Mutations and prognosis in primary myelofibrosis A M Vannucchi, T L Lasho, P Guglielmelli, F Biamonte, A Pardanani, A Pereira, C Finke, J Score, N Gangat, C Mannarelli, R P Ketterling, G Rotunno, R A Knudson, M C Susini, R R Laborde, A Spolverini, A Pancrazzi, L Pieri, R Manfredini, E Tagliafico, R Zini, A Jones, K Zoi, A Reiter, A Duncombe, D Pietra, E Rumi, F Cervantes, G Barosi, M Cazzola, N C P Cross, A Tefferi Leukemia, 2013
The ERCC2 Gln/Gln polymorphism at codon 751 is not associated with leukaemic transformation in primary myelofibrosis Maria C. Susini, Paola Guglielmelli, Ambra Spolverini, Flavia Biamonte, Carmela Mannarelli, Giovanni Barosi, Katerina Zoi, Andreas Reiter, Andrew Duncombe, Francisco Cervantes, Mario Cazzola, Nick Cross, Alessandro M. Vannucchi, the Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative (AGIMM) Investigators British Journal of Haematology, 2013
Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation Vittorio Rosti, Laura Villani, Roberta Riboni, Valentina Poletto, Elisa Bonetti, Lorenzo Tozzi, Gaetano Bergamaschi, Paolo Catarsi, Elena Dallera, Francesca Novara, Margherita Massa, Rita Campanelli, Gabriela Fois, Benedetta Peruzzi, Marco Lucioni, Paola Guglielmelli, Alessandro Pancrazzi, Giacomo Fiandrino, Orsetta Zuffardi, Umberto Magrini, Marco Paulli, Alessandro M. Vannucchi, Giovanni Barosi Blood, 2013
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2 J. Nangalia, C.E. Massie, E.J. Baxter, F.L. Nice, G. Gundem, D.C. Wedge, E. Avezov, J. Li, K. Kollmann, D.G. Kent, A. Aziz, A.L. Godfrey, J. Hinton, I. Martincorena, P. Van Loo, A.V. Jones, P. Guglielmelli, P. Tarpey, H.P. Harding, J.D. Fitzpatrick, C.T. Goudie, C.A. Ortmann, S.J. Loughran, K. Raine, D.R. Jones, A.P. Butler, J.W. Teague, S. O'Meara, S. McLaren, M. Bianchi, Y. Silber, D. Dimitropoulou, D. Bloxham, L. Mudie, M. Maddison, B. Robinson, C. Keohane, C. Maclean, K. Hill, K. Orchard, S. Tauro, M.-Q. Du, M. Greaves, D. Bowen, B.J.P. Huntly, C.N. Harrison, N.C.P. Cross, D. Ron, A.M. Vannucchi, E. Papaemmanuil, P.J. Campbell, A.R. Green New England Journal of Medicine, 2013
Molecular genetics in diagnosis and prognosis of philadelphia chromosome negative myeloproliferative neoplasms molecular genetics in MPNS Onkologie, 2012
Improving survival trends in primary myelofibrosis: An international study Francisco Cervantes, Brigitte Dupriez, Francesco Passamonti, Alessandro M. Vannucchi, Enrica Morra, John T. Reilly, Jean-Loup Demory, Elisa Rumi, Paola Guglielmelli, Elisa Roncoroni, Ayalew Tefferi, Arturo Pereira Journal of Clinical Oncology, 2012
Hydroxyurea-related toxicity in 3,411 patients with Ph'-negative MPN Elisabetta Antonioli, Paola Guglielmelli, Lisa Pieri, MariaChiara Finazzi, Elisa Rumi, Vincenzo Martinelli, Nicola Vianelli, Maria Luigia Randi, Irene Bertozzi, Valerio De Stefano, Tommaso Za, Elena Rossi, Marco Ruggeri, Elena Elli, Rossella Cacciola, Emma Cacciola, Enrico Pogliani, Francesco Rodeghiero, Michele Baccarani, Francesco Passamonti, Guido Finazzi, Alessandro Rambaldi, Alberto Bosi, Mario Cazzola, Tiziano Barbui, Alessandro M. Vannucchi, On behalf of the AGIMM Investigators American Journal of Hematology, 2012
Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies Ana Puda, Jelena D. Milosevic, Tiina Berg, Thorsten Klampfl, Ashot S. Harutyunyan, Bettina Gisslinger, Elisa Rumi, Daniela Pietra, Luca Malcovati, Chiara Elena, Michael Doubek, Michael Steurer, Natasa Tosic, Sonja Pavlovic, Paola Guglielmelli, Lisa Pieri, Alessandro M. Vannucchi, Heinz Gisslinger, Mario Cazzola, Robert Kralovics American Journal of Hematology, 2012
Does the nasogastric tube has a role in elective colo-rectal surgery? Il Giornale Di Chirurgia, 2012
EZH2 mutational status predicts poor survival in myelofibrosis Paola Guglielmelli, Flavia Biamonte, Joannah Score, Claire Hidalgo-Curtis, Francisco Cervantes, Margherita Maffioli, Tiziana Fanelli, Thomas Ernst, Nils Winkelman, Amy V. Jones, Katerina Zoi, Andreas Reiter, Andrew Duncombe, Laura Villani, Alberto Bosi, Giovanni Barosi, Nicholas C. P. Cross, Alessandro M. Vannucchi Blood, 2011
Safety and efficacy of everolimus, a mTOR inhibitor, as single agent in a phase 1/2 study in patients with myelofibrosis Paola Guglielmelli, Giovanni Barosi, Alessandro Rambaldi, Roberto Marchioli, Arianna Masciulli, Lorenzo Tozzi, Flavia Biamonte, Niccolò Bartalucci, Elisabetta Gattoni, Maria Letizia Lupo, Guido Finazzi, Alessandro Pancrazzi, Elisabetta Antonioli, Maria Chiara Susini, Lisa Pieri, Elisa Malevolti, Emilio Usala, Ubaldo Occhini, Alberto Grossi, Silvia Caglio, Simona Paratore, Alberto Bosi, Tiziano Barbui, Alessandro M. Vannucchi, on behalf of the AIRC-Gruppo Italiano Malattie Mieloproliferative (AGIMM) investigators Blood, 2011
Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression Thorsten Klampfl, Ashot Harutyunyan, Tiina Berg, Bettina Gisslinger, Martin Schalling, Klaudia Bagienski, Damla Olcaydu, Francesco Passamonti, Elisa Rumi, Daniela Pietra, Roland Jäger, Lisa Pieri, Paola Guglielmelli, Ilaria Iacobucci, Giovanni Martinelli, Mario Cazzola, Alessandro M. Vannucchi, Heinz Gisslinger, Robert Kralovics Blood, 2011
Increased risk of recurrent thrombosis in patients with essential thrombocythemia carrying the homozygous JAK2 V617F mutation for the GIMEMA Chronic Myeloproliferative Neoplasms Working Party, Valerio De Stefano, Tommaso Za, Elena Rossi, Alessandro M. Vannucchi, Marco Ruggeri, Elena Elli, Caterina Micò, Alessia Tieghi, Rossella R. Cacciola, Cristina Santoro, Nicola Vianelli, Paola Guglielmelli, Lisa Pieri, Francesca Scognamiglio, Emma Cacciola, Francesco Rodeghiero, Enrico M. Pogliani, Guido Finazzi, Luigi Gugliotta, Giuseppe Leone, Tiziano Barbui Annals of Hematology, 2010
Thrombosis in primary myelofibrosis: Incidence and risk factors Tiziano Barbui, Alessandra Carobbio, Francisco Cervantes, Alessandro M. Vannucchi, Paola Guglielmelli, Elisabetta Antonioli, Alberto Alvarez-Larrán, Alessandro Rambaldi, Guido Finazzi, Giovanni Barosi Blood, 2010
Animal models of myelofibrosis Alessandro M. Vannucchi, Jean-Luc Villeval, Orianne Wagner-Ballon, Paola Guglielmelli, Anna Rita Migliaccio Source Book of Models for Biomedical Research, 2008
Insights into JAK2-V617F mutation in CML Monica Bocchia, Alessandro M Vannucchi, Alessandro Gozzetti, Paola Guglielmelli, Giada Poli, Rosaria Crupi, Marzia Defina, Alberto Bosi, Lauria Francesco Lancet Oncology, 2007
Clinical profile of homozygous JAK2 617V>F mutation in patients with polycythemia vera or essential thrombocythemia Alessandro M. Vannucchi, Elisabetta Antonioli, Paola Guglielmelli, Alessandro Rambaldi, Giovanni Barosi, Roberto Marchioli, Rosa Maria Marfisi, Guido Finazzi, Vittoria Guerini, Fabrizio Fabris, Maria Luigia Randi, Valerio De Stefano, Sabrina Caberlon, Agostino Tafuri, Marco Ruggeri, Giorgina Specchia, Vincenzo Liso, Edoardo Rossi, Enrico Pogliani, Luigi Gugliotta, Alberto Bosi, Tiziano Barbui Blood, 2007
Anaemia characterises patients with myelofibrosis harbouring Mpl W515L/K mutation Paola Guglielmelli, Alessandro Pancrazzi, Gaetano Bergamaschi, Vittorio Rosti, Laura Villani, Elisabetta Antonioli, Alberto Bosi, Giovanni Barosi, Alessandro M. Vannucchi, for the GIMEMA‐Italian Registry of Myelofibrosis, the MPD Research Consortium, Chicago, IL, USA British Journal of Haematology, 2007
Describing the use of ruxolitinib for the treatment of myelofibrosis: a plain language summary of the ROMEI early study results M Breccia, P Guglielmelli, C Castiglioni, F Palandri, F Passamonti Future Oncology, 1-11 , 2026 2026
Autoimmune and Inflammatory Diseases in Polycythemia Vera and Essential Thrombocythemia: Impact on Disease Outcomes and Comorbidities GG Loscocco, F Aperna, M Iftikhar, P Faldu, MS Rana, A Pardanani, ... American journal of hematology , 2026 2026
APL‐like subset within NPM1 ‐mutated AML: A distinct immunophenotype correlating with early vascular complications F Mannelli, F Crupi, S Bencini, M Feuring, G Ciolli, M Piccini, M Frigeni, ... HemaSphere 10 (4), e70307 , 2026 2026
Genomic profiling for decision-making in post–polycythemia vera and post–essential thrombocythemia myelofibrosis B Mora, F Palandri, P Guglielmelli, AT Kuykendall, M Maffioli, A Iurlo, ... Blood , 2026 2026 Citations: 1
Genomic structural variations contribute to inform prognosis in patients with cytogenetically normal acute myeloid leukemia N Bartalucci, F Mannelli, D Tarantino, A Enderti, S Romagnoli, D Colazzo, ... Blood Cancer Journal , 2026 2026
CO59| JAK2 46/1 haplotype and JAK2 variant allelic frequency correlate with the development of polycythemic phenotype in JAK2-mutated essential thrombocytemia patients G Capecchi, C Maccari, GG Loscocco, V Boldrini, G Rotunno, F Gesullo, ... Haematologica 111 (s1) , 2026 2026
CO57| Molecular characterization of a cohort of patients with polycythemia vera: a single-center study E Nacca, C Ghetti, F Vanderwert, V Boldrini, L Fagiolo, G Rotunno, ... Haematologica 111 (s1) , 2026 2026
P018| Improving diagnostic standardization in myeloproliferative neoplasms: results from the Italian JakNet Program F Gesullo, E Nacca, G Rotunno, F Vanderwert, R Cucci, G Polese, ... Haematologica 111 (s1) , 2026 2026
P054| Discontinuation of venetoclax-based therapies in molecularly selected patients with acute myeloid leukemia in complete remission G Ciolli, F Mannelli, M Frigeni, M Piccini, B Scappini, F Crupi, E Quinti, ... Haematologica 111 (s1) , 2026 2026
CO62| CD9 defines the disease-propagating hematopoietic stem cell population in myelofibrosis R Norfo, L Tavernari, A Neroni, C Tombari, S Rontauroli, M Mirabile, ... Haematologica 111 (s1) , 2026 2026
Clinical Outcomes of Ruxolitinib Treatment in Patients With IPSS Intermediate‐1‐Risk Myelofibrosis: Interim Analysis From an Italian, Prospective Study (ROMEI) P Guglielmelli, M Breccia, F Mendicino, M Martelli, N Di Renzo, ... Hematological Oncology 44 (2), e70178 , 2026 2026
Artificial intelligence differentiates prefibrotic primary myelofibrosis with thrombocytosis from essential thrombocythemia using digitized bone marrow biopsy images A Srisuwananukorn, GG Loscocco, JM Dolezal, AT Kuykendall, R Santi, ... Leukemia, 1-9 , 2026 2026
The Role and Impact of Non-driver Gene Mutations in Myelofibrosis V Boldrini, P Guglielmelli, AM Vannucchi Current Hematologic Malignancy Reports 21 (1), 3 , 2026 2026
Health Care Utilization Databases obtained from health system inform outcome for ruxolitinib treatment in patients with myelofibrosis B Mora, M Franchi, L Margotto, O Leoni, D D'ippoliti, E Carloni, I Cozzi, ... HemaSphere 10 (2), e70316 , 2026 2026
Understanding Triple Negative Myeloproliferative Neoplasms and Identifying Molecular Drivers V Boldrini, GG Loscocco, P Guglielmelli, N Gangat, AM Vannucchi, ... Current Hematologic Malignancy Reports 21 (1), 1 , 2026 2026 Citations: 1
Clinical Experience With Venetoclax-Based Combinations for Relapsed/Refractory or MRD-Positive NPM1-Mutated Acute Myeloid Leukemia. M Piccini, N Gangat, F Mannelli, B Scappini, G Ciolli, F Crupi, A Pasquini, ... American Journal of Hematology, 1-5 , 2026 2026
Genome-wide analysis defines genetic determinants of MPN subtypes and identifies a sex-specific association at CDH22 / CD40 WJ Tapper, AAZ Dawoud, J Score, AJ Chase, EJ Baxter, J Ewing, L Wallis, ... Blood 146 (26), 3228-3233 , 2025 2025 Citations: 3
A Novel, Ruxolitinib-Sensitive, CCDC6:: JAK2 Fusion Gene in a Patient With Atypical, JAK2 Unmutated, Polycythemia Vera-Like, Myeloproliferative Neoplasm. N Bartalucci, D Tarantino, GG Loscocco, A Enderti, D Colazzo, R Santi, ... American Journal of Hematology 101 (2), 379-383 , 2025 2025
Health‐related quality of life and symptom profile of patients with BCR::ABL1 ‐negative myeloproliferative neoplasms: Real‐world evidence from the GIMEMA … G Caocci, A Costa, F Palandri, P Guglielmelli, A Patriarca, A Iurlo, ... HemaSphere 9 (12), e70274 , 2025 2025
Combinatorial BCL2/BCL2L1 expression predicts clinical response to ruxolitinib in myelofibrosis G Coltro, V Videschi, F Gesullo, F Violi, M Balliu, AM Vannucchi, ... Biomarker Research 13 (1), 151 , 2025 2025
MOST CITED SCHOLAR PUBLICATIONS
Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2 J Nangalia, CE Massie, EJ Baxter, FL Nice, G Gundem, DC Wedge, ... New England Journal of Medicine 369 (25), 2391-2405 , 2013 2013 Citations: 2412
A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and … F Passamonti, F Cervantes, AM Vannucchi, E Morra, E Rumi, A Pereira, ... Blood, The Journal of the American Society of Hematology 115 (9), 1703-1708 , 2010 2010 Citations: 1262
Long-term survival and blast transformation in molecularly annotated essential thrombocythemia, polycythemia vera, and myelofibrosis A Tefferi, P Guglielmelli, DR Larson, C Finke, EA Wassie, L Pieri, ... Blood, The Journal of the American Society of Hematology 124 (16), 2507-2513 , 2014 2014 Citations: 1007
Mutations and prognosis in primary myelofibrosis AM Vannucchi, TL Lasho, P Guglielmelli, F Biamonte, A Pardanani, ... Leukemia 27 (9), 1861-1869 , 2013 2013 Citations: 983
The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms: document summary and in-depth discussion T Barbui, J Thiele, H Gisslinger, HM Kvasnicka, AM Vannucchi, ... Blood cancer journal 8 (2), 15 , 2018 2018 Citations: 868
Classification and personalized prognosis in myeloproliferative neoplasms J Grinfeld, J Nangalia, EJ Baxter, DC Wedge, N Angelopoulos, R Cantrill, ... New England Journal of Medicine 379 (15), 1416-1430 , 2018 2018 Citations: 763
Effect of mutation order on myeloproliferative neoplasms CA Ortmann, DG Kent, J Nangalia, Y Silber, DC Wedge, J Grinfeld, ... New England Journal of Medicine 372 (7), 601-612 , 2015 2015 Citations: 707
MIPSS70: mutation-enhanced international prognostic score system for transplantation-age patients with primary myelofibrosis P Guglielmelli, TL Lasho, G Rotunno, M Mudireddy, C Mannarelli, ... Journal of Clinical Oncology 36 (4), 310-318 , 2018 2018 Citations: 658
Clinical profile of homozygous JAK2 617V>F mutation in patients with polycythemia vera or essential thrombocythemia AM Vannucchi, E Antonioli, P Guglielmelli, A Rambaldi, G Barosi, ... Blood, The Journal of the American Society of Hematology 110 (3), 840-846 , 2007 2007 Citations: 653
Impact of calreticulin mutations on clinical and hematological phenotype and outcome in essential thrombocythemia G Rotunno, C Mannarelli, P Guglielmelli, A Pacilli, A Pancrazzi, L Pieri, ... Blood, The Journal of the American Society of Hematology 123 (10), 1552-1555 , 2014 2014 Citations: 555
Clinical effect of driver mutations of JAK2 , CALR , or MPL in primary myelofibrosis E Rumi, D Pietra, C Pascutto, P Guglielmelli, A Martínez-Trillos, I Casetti, ... Blood, The Journal of the American Society of Hematology 124 (7), 1062-1069 , 2014 2014 Citations: 534
Prospective identification of high-risk polycythemia vera patients based on JAK2V617F allele burden AM Vannucchi, E Antonioli, P Guglielmelli, G Longo, A Pancrazzi, ... Leukemia 21 (9), 1952-1959 , 2007 2007 Citations: 510
MIPSS70+ version 2.0: mutation and karyotype-enhanced international prognostic scoring system for primary myelofibrosis A Tefferi, P Guglielmelli, TL Lasho, N Gangat, RP Ketterling, A Pardanani, ... Journal of clinical oncology: official journal of the American Society of … , 2018 2018 Citations: 467
Recurrent thrombosis in patients with polycythemia vera and essential thrombocythemia: incidence, risk factors, and effect of treatments V De Stefano, T Za, E Rossi, AM Vannucchi, M Ruggeri, E Elli, C Micò, ... haematologica 93 (3), 372-380 , 2008 2008 Citations: 453
IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic-or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis A Tefferi, TL Lasho, O Abdel-Wahab, P Guglielmelli, J Patel, ... Leukemia 24 (7), 1302-1309 , 2010 2010 Citations: 409
A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis F Passamonti, T Giorgino, B Mora, P Guglielmelli, E Rumi, M Maffioli, ... Leukemia 31 (12), 2726-2731 , 2017 2017 Citations: 402
Clinical correlates of JAK2V617F presence or allele burden in myeloproliferative neoplasms: a critical reappraisal AM Vannucchi, E Antonioli, P Guglielmelli, A Pardanani, A Tefferi Leukemia 22 (7), 1299-1307 , 2008 2008 Citations: 401
The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients P Guglielmelli, TL Lasho, G Rotunno, J Score, C Mannarelli, A Pancrazzi, ... Leukemia 28 (9), 1804-1810 , 2014 2014 Citations: 388
Targeted deep sequencing in polycythemia vera and essential thrombocythemia A Tefferi, TL Lasho, P Guglielmelli, CM Finke, G Rotunno, Y Elala, ... Blood advances 1 (1), 21-30 , 2016 2016 Citations: 376
Advances in understanding and management of myeloproliferative neoplasms AM Vannucchi, P Guglielmelli, A Tefferi CA: a cancer journal for clinicians 59 (3), 171-191 , 2009 2009 Citations: 371