Monoclonal B-Cell Lymphocytosis: The Silent Clone the Haematologists Should Not Neglect Andrea Serafin, Emanuela Sant’Antonio, Fabrizio Mavilia, Francesca Gandini, Stefano De Pretis, Lydia Scarfò, Paolo Ghia Hematological Oncology, 2025 Monoclonal B‐cell lymphocytosis (MBL) is a hematologic condition defined by the presence of a small clonal B‐cell population in the peripheral blood, without clinical or laboratory evidence of lymphoproliferative disorders. It is classified into low‐count (LC‐MBL) and high‐count (HC‐MBL) subtypes based on clonal size. HC‐MBL shares genetic and biological features with early‐stage chronic lymphocytic leukemia (CLL), has a well‐established 1%–2% annual risk of progression, and is associated with an increased risk of infections, second malignancies and a reduced response to vaccines due to immune dysfunction. LC‐MBL, on the other hand, is a distinct entity with a lower likelihood of progression, but its potential impact on immune function remains unclear. While some studies suggest an association with increased infection risk and immune alterations, further research is needed to clarify its clinical significance. Beyond the risk of progression, MBL is increasingly recognized as a condition requiring careful management due to its broader implications on immune function and cancer susceptibility. Given these risks, preventive strategies are essential for all individuals with MBL, including adherence to cancer screening programs, vaccinations, smoking cessation, sun protection, and a healthy lifestyle to mitigate potential complications.
Loss of CYLD promotes splenic marginal zone lymphoma Athanasios Pseftogas, Jessica Bordini, Silvia Heltai, Ferdinando Bonfiglio, Georgios Gavriilidis, Vasileios Vasileiou, Sofoklis Keisaris, Daniela Belloni, Caterina Taccetti, Pamela Ranghetti, Eleonora Perotta, Michela Frenquelli, Uday Aditya Sarkar, Elisa Albi, Francesca Martini, Emmanuela Sant'Antonio, Fabrizio Mavilia, Fotis Psomopoulos, Manasori Daibata, José Ángel Martínez Climent, George Mosialos, Davide Rossi, Alessandro Campanella, Lydia Scarfò, Kostas Stamatopoulos, Konstantinos Xanthopoulos, Paolo Ghia Hemasphere, 2025 Splenic marginal zone lymphoma (SMZL) is a distinct clinical and pathological entity among marginal zone lymphomas. Genetic and microenvironmental factors leading to aberrant activation of the NF‐κB pathway have been implicated in SMZL pathogenesis. CYLD is a negative regulator of NF‐κB and other signaling pathways acting as a deubiquitinase of regulatory molecules and has been reported as a tumor suppressor in different types of cancer, including B‐cell malignancies. To assess whether CYLD is implicated in the natural history of SMZL, we profiled primary cells from patients with SMZL and SMZL cell lines for CYLD expression and functionality. We report that CYLD is downregulated in patients with SMZL and that CYLD ablation in vitro leads to NF‐κB pathway hyperactivation, promoting the proliferation of SMZL cells. In addition, we found that CYLD deficiency was associated with increased migration of SMZL cells in vitro, through CCR7 receptor signaling, and with increased dissemination in vivo. CYLD loss was sufficient to induce BcR signaling, conferring increased resistance to ibrutinib treatment in vitro. In summary, our work uncovers a novel role of CYLD as a key regulator in SMZL pathogenesis, dissemination, and resistance to targeted agents. On these grounds, CYLD could be proposed as a novel target for patient stratification and personalized interventions.
Additional booster doses in patients with chronic lymphocytic leukemia induce humoral and cellular immune responses to SARS-CoV-2 similar to natural infection regardless ongoing treatments: A study by ERIC, the European Research Initiative on CLL A. Campanella, A. Capasso, S. Heltai, C. Taccetti, E. Albi, Y. Herishanu, S. Haggenburg, T. Chatzikonstantinou, M. Doubek, M. Kättström, K. Giannopoulos, M. Simkovic, C. Moreno, M. Massaia, H. Bumbea, S. Alshemmari, P. Ranghetti, E. Perotta, F. Martini, E. Sant'Antonio, M. Colia, C. Combi, S. Levi, A. P. Kater, M. Hazenberg, I. S. Nijhof, Q. Hofsink, C. Demosthenous, J. Kotaskova, J. Zaleska, F. Vrbacky, A. Mora Raya, D. Bisogno, I. E. Tripoli, V. M. Popov, V. Roman, N. Stavroyianni, M. Karypidou, E. Scarano, M. Locatelli, M. Frenquelli, L. Scarfò, K. Stamatopoulos, P. Ghia American Journal of Hematology, 2024 Profound immune dysregulation and impaired response to the SARS-CoV-2 vaccine put patients with chronic lymphocytic leukemia (CLL) at risk of severe COVID-19. We compared humoral memory and T-cell responses after booster dose vaccination or breakthrough infection. (Green) Quantitative determination of anti-Spike specific antibodies. Booster doses increased seroconversion rate and antibody titers in all patient categories, ultimately generating humoral responses similar to those observed in the postinfection cohort. In detail, humoral response with overscale median antibody titers arose in >80% of patients in watch and wait, off-therapy in remission, or under treatment with venetoclax single-agent. Anti-CD20 antibodies and active treatment with BTK inhibitors (BTKi) represent limiting factors of humoral response, still memory mounted in ~40% of cases following booster doses or infection. (Blue) Evaluation of SARS-CoV-2-specific T-cell responses. Number of T-cell functional activation markers documented in each patient. The vast majority of patients, including those seronegative, developed T-cell responses, qualitatively similar between treatment groups or between vaccination alone and infection cases. These data highlight the efficacy of booster doses in eliciting T-cell immunity independently of treatment status and support the use of additional vaccination boosters to stimulate humoral immunity in patients on active CLL-directed treatments.
Assessment of the efficacy and tolerability of ruxolitinib for the treatment of myelofibrosis patients in a real-life setting: An Italian MYNERVA Project Giacomo Coltro, Emanuela Sant'Antonio, Giuseppe A. Palumbo, Francesco Mannelli, Valerio De Stefano, Marco Ruggeri, Elena M. Elli, Roberta Zanotti, Oscar Borsani, Irene Bertozzi, Andrea Duminuco, Silvia Betti, Giuseppe Carli, Fabrizio Cavalca, Ilaria Tanasi, Elisa Rumi, Maria L. Randi, Bruno Garibaldi, Giuseppe G. Loscocco, Paola Guglielmelli, Alessandro M. Vannucchi Cancer Medicine, 2023 BACKGROUND Incorporating real-world data in the drug development process allows the improvement of health outcomes by providing better representation of actual patterns of drug safety and efficacy. AIMS AND METHODS Here, we present the results of a retroprospective, observational real-life study of 154 patients with myelofibrosis treated with ruxolitinib in a real-life setting in seven Italian centers of the MYNERVA project. RESULTS Median drug exposure was 29 (range, 3-98) months. Discontinuation rate was 27% after a median time of 13 (range, 3-61). While hematological toxicities were in line with previous findings, infections occurred frequently, representing a not negligible cause of discontinuation and death. Anemia, symptoms, and spleen responses were obtained at any time in 23%, 91%, and 68% of patients, respectively; most patients achieved their responses by week 24. Larger splenomegaly and delayed treatment initiation correlated with lower spleen response at 24 weeks. Spleen response was associated with a superior overall survival, regardless of DIPSS. Of interest, both achievement and loss of spleen response had prognostic implications. DISCUSSION AND CONCLUSION Overall, our findings provide insights on the efficacy and safety of ruxolitinib in a real-world, multicenter cohort of Italian MF patients.
CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL Antonella Capasso, Elisa Albi, Luana Schiattone, Francesca Martini, Emanuela Sant'Antonio, Lydia Scarfò, Pamela Ranghetti, Michela Frenquelli, Alessandro Campanella, Eleonora Perotta, Silvia Heltai, Maria Colia, Paolo Ghia Clinical Lymphoma Myeloma and Leukemia, 2022
Management of Myelofibrosis during Treatment with Ruxolitinib: A Real-World Perspective in Case of Resistance and/or Intolerance Massimo Breccia, Francesca Palandri, Paola Guglielmelli, Giuseppe Alberto Palumbo, Alessandra Malato, Francesco Mendicino, Alessandra Ricco, Emanuela Sant’Antonio, Mario Tiribelli, Alessandra Iurlo Current Oncology, 2022 The development and approval of ruxolitinib, the first JAK1/2 inhibitor indicated to treat myelofibrosis, has improved patient outcomes, with higher spleen and symptoms responses, improved quality of life, and overall survival. Despite this, several unmet needs remain, including the absence of resistance criteria, suboptimal response, the timing of allogeneic transplant, and the management of patients in case of intolerance. Here, we report the results of the second survey led by the “MPN Lab” collaboration, which aimed to report physicians’ perspectives on these topics. As in our first survey, physicians were selected throughout Italy, and we included those with extensive experience in treating myeloproliferative neoplasms and those with less experience representing clinical practice in the real world. The results presented here, summarized using descriptive analyses, highlight the need for a clear definition of response to ruxolitinib as well as recommendations to guide the management of ruxolitinib under specific conditions including anemia, thrombocytopenia, infections, and non-melanoma skin cancers.
Autoantibodies against type I IFNs in patients with Ph-negative myeloproliferative neoplasms Oscar Borsani, Paul Bastard, Jérémie Rosain, Adrian Gervais, Emanuela Sant’Antonio, Daniele Vanni, Ilaria Carola Casetti, Daniela Pietra, Chiara Trotti, Silvia Catricalà, Virginia Valeria Ferretti, Luca Malcovati, Luca Arcaini, Jean-Laurent Casanova, Alessandro Borghesi, Elisa Rumi Blood, 2022 International audience
New Insights into Neuropeptides Regulation of the Immune System and Hemopoiesis: Effects on Hematologic Malignancies Alessandro Allegra, Emanuela Sant’Antonio, Caterina Musolino, Roberta Ettari Current Medicinal Chemistry, 2022 :Several neurotransmitters and neuropeptides were reported to join to or to cooperate with different cells of the immune system, bone marrow, and peripheral cells and numerous data support that neuroactive molecules might control immune system activity and hemopoiesis operating on lymphoid organs, and the primary hematopoietic unit, the hematopoietic niche. Furthermore, many compounds seem to be able to take part to the leukemogenesis and lymphomagenesis process, and in the onset of multiple myeloma. In this review, we will assess the possibility that neurotransmitters and neuropeptides may have a role in the onset of haematological neoplasms, may affect the response to treatment or may represent a useful starting point for a new therapeutic approach. More in vivo investigations are needed to evaluate neuropeptide’s role in haematological malignancies and the possible utilization as an antitumor therapeutic target. Comprehending the effect of the pharmacological administration of neuropeptide modulators on hematologic malignancies opens up new possibilities in curing clonal hematologic diseases to achieve more satisfactory outcomes.
Facing erythrocytosis: Results of an international physician survey Elisa Rumi, Mary F. McMullin, Claire Harrison, Martin H. Ellis, Merav Barzilai, Nadav Sarid, Ruben Mesa, Chiara Paoli, Anna Angona, Emanuela Sant'Antonio, Virginia V. Ferretti, Chiara Cavalloni, Ilaria C. Casetti, Chiara Trotti, Tiziano Barbui American Journal of Hematology, 2019
Diagnosis and management of prefibrotic myelofibrosis Elisa Rumi, Emanuela Sant’Antonio, Emanuela Boveri, Daniela Pietra, Chiara Cavalloni, Elisa Roncoroni, Cesare Astori, Luca Arcaini Expert Review of Hematology, 2018
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
Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia E. Rumi, I. Bertozzi, I. C. Casetti, E. Roncoroni, C. Cavalloni, M. Bellini, E. Sant'Antonio, M. Gotti, V. V. Ferretti, C. Milanesi, E. Peroni, D. Pietra, C. Astori, M. L. Randi, M. Cazzola, on behalf of the Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative Investigators Haematologica, 2015
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
Somatic mutations of calreticulin in myeloproliferative neoplasms Thorsten Klampfl, Heinz Gisslinger, Ashot S. Harutyunyan, Harini Nivarthi, Elisa Rumi, Jelena D. Milosevic, Nicole C.C. Them, Tiina Berg, Bettina Gisslinger, Daniela Pietra, Doris Chen, Gregory I. Vladimer, Klaudia Bagienski, Chiara Milanesi, Ilaria Carola Casetti, Emanuela Sant'Antonio, Virginia Ferretti, Chiara Elena, Fiorella Schischlik, Ciara Cleary, Melanie Six, Martin Schalling, Andreas Schönegger, Christoph Bock, Luca Malcovati, Cristiana Pascutto, Giulio Superti-Furga, Mario Cazzola, Robert Kralovics New England Journal of Medicine, 2013
Epigenetic therapy in myelodysplastic syndromes Caterina Musolino, Emanuela Sant’Antonio, Giuseppa Penna, Andrea Alonci, Sabina Russo, Angela Granata, Alessandro Allegra European Journal of Haematology, 2010
RECENT SCHOLAR PUBLICATIONS
CLINICAL AND GENOMIC PATTERNS OF DISEASE PROGRESSION IN CLL PATIENTS TREATED WITH FIXED-DURATION VERSUS CONTINUOUS TARGETED THERAPIES A Serafin, F Angotzi, A Bevilacqua, A Cellini, M D'Antiga, L Bonaldi, ... Haematologica 111 (1), 1-1 , 2026 2026
Monoclonal B‐cell lymphocytosis: the silent clone the haematologists should not neglect A Serafin, E Sant’Antonio, F Mavilia, F Gandini, S De Pretis, L Scarfò, ... Hematological Oncology 43, e70084 , 2025 2025 Citations: 2
Severe COVID-19 Infection in Patients with Chronic Lymphocytic Leukemia or Indolent B-Cell Non-Hodgkin Lymphoma Who Received Pre-Exposure Prophylaxis with Tixagevimab and … GM Rigolin, A Urso, S Soddu, R Moia, R Dondolin, A Olivieri, I Scortechini, ... Blood 144, 1872 , 2024 2024
Additional booster doses in patients with chronic lymphocytic leukemia induce humoral and cellular immune responses to SARS‐CoV‐2 similar to natural infection regardless … A Campanella, A Capasso, S Heltai, C Taccetti, E Albi, Y Herishanu, ... American Journal of Hematology 99 (4), 745-750 , 2024 2024 Citations: 15
Outcomes of Venetoclax Retreatment after MRD-Guided Venetoclax+/-Ibrutinib: Results of the Improve Study E Albi, L Scarfo, S Heltai, E Scarano, L Schiattone, L Farina, R Moia, ... Blood 142, 6521 , 2023 2023 Citations: 3
P1517: HUMORAL AND CELLULAR IMMUNE RESPONSES TO SARS-COV-2 NATURAL INFECTION OR VACCINATION IN PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKEMIA (CLL): A STUDY BY ERIC, THE EUROPEAN … A Campanella, A Capasso, C Taccetti, S Heltai, E Albi, Y Herishanu, ... HemaSphere 7 (S3), e483427a , 2023 2023
P646: VENETOCLAX RETREATMENT AFTER MRD-GUIDED VENETOCLAX+/-IBRUTINIB: THE IMPROVE STUDY COHORT L Scarfò, S Heltai, E Albi, E Scarano, L Schiattone, L Farina, R Moia, ... HemaSphere 7 (S3), e8082529 , 2023 2023 Citations: 3
Assessment of the efficacy and tolerability of ruxolitinib for the treatment of myelofibrosis patients in a real‐life setting: An Italian MYNERVA Project G Coltro, E Sant'Antonio, GA Palumbo, F Mannelli, V De Stefano, ... Cancer Medicine 12 (7), 8166-8171 , 2023 2023 Citations: 15
Ibrutinib in relapsed/refractory patients with Waldenström macroglobulinemia: a real-life, retrospective study on behalf of the “RTL”(regional Tuscan lymphoma network) E Cencini, I Romano, F Ghio, C Camerini, I Bertaggia, R Giachetti, ... Annals of Hematology 102 (4), 841-849 , 2023 2023 Citations: 6
Germline Predisposition in the Field of Myeloproliferative Neoplasms E Sant’Antonio, O Borsani, E Rumi Hematological Cancer Pathophysiology: An Interdisciplinary Approach, 143-158 , 2022 2022
Molecular Characterization of Response/Loss-of-Response to Ruxolitinib in Patients with Myelofibrosis P Guglielmelli, FI Vanderwert, S Romagnoli, G Coltro, GG Loscocco, ... Blood, The Journal of the American Society of Hematology 140 (Supplement 1 … , 2022 2022 Citations: 1
CLL-461 humoral response to COVID-19 vaccine: a challenge in CLL A Capasso, E Albi, L Schiattone, F Martini, E Sant'Antonio, L Scarfò, ... Clinical Lymphoma Myeloma and Leukemia 22, S279-S280 , 2022 2022 Citations: 2
Poster: CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL A Capasso, E Albi, L Schiattone, F Martini, E Sant'Antonio, L Scarfò, ... Clinical Lymphoma, Myeloma & Leukemia 22, S143 , 2022 2022
Management of myelofibrosis during treatment with ruxolitinib: a real-world perspective in case of resistance and/or intolerance M Breccia, F Palandri, P Guglielmelli, GA Palumbo, A Malato, F Mendicino, ... Current Oncology 29 (7), 4970-4980 , 2022 2022 Citations: 4
Haematological malignancies in relatives of patients affected with myeloproliferative neoplasms D Vanni, O Borsani, Y Nannya, E Sant'Antonio, C Trotti, IC Casetti, ... EJHaem 3 (2), 475-479 , 2022 2022 Citations: 1
Autoantibodies against type I IFNs in patients with Ph-negative myeloproliferative neoplasms O Borsani, P Bastard, J Rosain, A Gervais, E Sant’Antonio, D Vanni, ... Blood, The Journal of the American Society of Hematology 139 (17), 2716-2720 , 2022 2022 Citations: 6
New Insights into Neuropeptides Regulation of the Immune System and Hemopoiesis: Effects on Hematologic Malignancies A Allegra, E Sant’Antonio, C Musolino, R Ettari Current Medicinal Chemistry 29 (14), 2412-2437 , 2022 2022
Philadelphia chromosome-negative myeloproliferative neoplasms in younger adults: a critical discussion of unmet medical needs, with a focus on pregnancy E Sant'Antonio, O Borsani, C Camerini, C Botta, M Santoro, A Allegra, ... Blood Reviews 52, 100903 , 2022 2022 Citations: 4
Unusual presentation of extranodal diffuse large B-cell lymphoma in a solid-organ recipient during long-term immunosuppressive treatment C Camerini, E Sant’Antonio, A Ginori, M Pellegri, C De Gaudio, E Banti, ... Tumori Journal 107 (6), NP127-NP130 , 2021 2021
Autoantibodies Against Type I IFNs in Patients with Ph-Negative Myeloproliferative Neoplasms O Borsani, P Bastard, J Rosain, A Gervais, E Sant'Antonio, D Vanni, ... Blood 138, 3587 , 2021 2021
MOST CITED SCHOLAR PUBLICATIONS
Somatic mutations of calreticulin in myeloproliferative neoplasms T Klampfl, H Gisslinger, AS Harutyunyan, H Nivarthi, E Rumi, JD Milosevic, ... New England Journal of Medicine 369 (25), 2379-2390 , 2013 2013 Citations: 2654
JAK2 or CALR mutation status defines subtypes of essential thrombocythemia with substantially different clinical course and outcomes E Rumi, D Pietra, V Ferretti, T Klampfl, AS Harutyunyan, JD Milosevic, ... Blood, The Journal of the American Society of Hematology 123 (10), 1544-1551 , 2014 2014 Citations: 821
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
Differential clinical effects of different mutation subtypes in CALR-mutant myeloproliferative neoplasms D Pietra, E Rumi, VV Ferretti, CA Di Buduo, C Milanesi, C Cavalloni, ... Leukemia 30 (2), 431-438 , 2016 2016 Citations: 361
Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL -mutated myeloproliferative neoplasms E Rumi, D Pietra, P Guglielmelli, R Bordoni, I Casetti, C Milanesi, ... Blood, The Journal of the American Society of Hematology 121 (21), 4388-4395 , 2013 2013 Citations: 132
High rate of recurrent venous thromboembolism in patients with myeloproliferative neoplasms and effect of prophylaxis with vitamin K antagonists V De Stefano, M Ruggeri, F Cervantes, A Alvarez-Larrán, A Iurlo, ... Leukemia 30 (10), 2032-2038 , 2016 2016 Citations: 111
Epidemiology and clinical relevance of mutations in postpolycythemia vera and postessential thrombocythemia myelofibrosis: a study on 359 patients of the AGIMM group G Rotunno, A Pacilli, V Artusi, E Rumi, M Maffioli, F Delaini, G Brogi, ... American journal of hematology 91 (7), 681-686 , 2016 2016 Citations: 111
CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis E Rumi, AS Harutyunyan, D Pietra, JD Milosevic, IC Casetti, M Bellini, ... Blood, The Journal of the American Society of Hematology 123 (15), 2416-2419 , 2014 2014 Citations: 106
RAS / CBL mutations predict resistance to JAK inhibitors in myelofibrosis and are associated with poor prognostic features G Coltro, G Rotunno, L Mannelli, C Mannarelli, S Fiaccabrino, ... Blood advances 4 (15), 3677-3687 , 2020 2020 Citations: 89
Splanchnic vein thromboses associated with myeloproliferative neoplasms: an international, retrospective study on 518 cases E Sant'Antonio, P Guglielmelli, L Pieri, M Primignani, ML Randi, ... American journal of hematology 95 (2), 156-166 , 2020 2020 Citations: 83
Clinical course and outcome of essential thrombocythemia and prefibrotic myelofibrosis according to the revised WHO 2016 diagnostic criteria E Rumi, E Boveri, M Bellini, D Pietra, VV Ferretti, E Sant’Antonio, ... Oncotarget 8 (60), 101735 , 2017 2017 Citations: 81
Prognostic impact of bone marrow fibrosis in primary myelofibrosis. A study of the AGIMM group on 490 patients P Guglielmelli, G Rotunno, A Pacilli, E Rumi, V Rosti, F Delaini, M Maffioli, ... American journal of hematology 91 (9), 918-922 , 2016 2016 Citations: 77
Novel therapeutic strategies in multiple myeloma: role of the heat shock protein inhibitors A Allegra, E Sant’Antonio, G Penna, A Alonci, A D’Angelo, S Russo, ... European journal of haematology 86 (2), 93-110 , 2011 2011 Citations: 55
Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia E Rumi, I Bertozzi, IC Casetti, E Roncoroni, C Cavalloni, M Bellini, ... Haematologica 100 (11), e443 , 2015 2015 Citations: 52
Epigenetic therapy in myelodysplastic syndromes C Musolino, E Sant’Antonio, G Penna, A Alonci, S Russo, A Granata, ... European journal of haematology 84 (6), 463-473 , 2010 2010 Citations: 47
A journey through infectious risk associated with ruxolitinib E Sant’Antonio, M Bonifacio, M Breccia, E Rumi British Journal of Haematology 187 (3), 286-295 , 2019 2019 Citations: 44
The role of allogeneic stem-cell transplant in myelofibrosis in the era of JAK inhibitors: a case-based review M Tiribelli, F Palandri, E Sant’Antonio, M Breccia, M Bonifacio Bone Marrow Transplantation 55 (4), 708-716 , 2020 2020 Citations: 41
Unmet clinical needs in the management of CALR-mutated essential thrombocythaemia: a consensus-based proposal from the European LeukemiaNet A Alvarez-Larrán, E Sant'Antonio, C Harrison, JJ Kiladjian, ... The Lancet Haematology 8 (9), e658-e665 , 2021 2021 Citations: 34
The genetic basis of primary myelofibrosis and its clinical relevance E Rumi, C Trotti, D Vanni, IC Casetti, D Pietra, E Sant’Antonio International Journal of Molecular Sciences 21 (23), 8885 , 2020 2020 Citations: 31
Diagnosis and management of prefibrotic myelofibrosis E Rumi, E Sant’Antonio, E Boveri, D Pietra, C Cavalloni, E Roncoroni, ... Expert review of hematology 11 (7), 537-545 , 2018 2018 Citations: 27