Meletios A. Dimopoulos
梅莱蒂奥斯·迪莫普洛斯
MD
Professor and Chairman, Department of Clinical Therapeutics, National and Kapodistrian University of Athens; Head, Department of Hematology, Alexandra General Hospital雅典国立卡波迪斯特里亚大学临床治疗系主任及教授;亚历山德拉总医院血液学科主任
👥Biography 个人简介
Meletios A. Dimopoulos, MD is Professor and Chairman of the Department of Clinical Therapeutics at the National and Kapodistrian University of Athens and Head of Hematology at Alexandra General Hospital. He is among the most cited hematologists in the world and is the principal co-investigator of the POLLUX and CASTOR trials — two seminal phase III studies that established daratumumab combinations as the standard of care for relapsed/refractory multiple myeloma. The POLLUX trial (NEJM 2016) demonstrated that daratumumab plus lenalidomide/dexamethasone (D-Rd) significantly improved PFS compared with Rd alone, while CASTOR (NEJM 2016) showed similar superiority for daratumumab plus bortezomib/dexamethasone (D-VD) — together leading to the FDA approvals that transformed relapsed myeloma management. Dr. Dimopoulos is also the world's foremost expert on Waldenström macroglobulinemia (WM), having co-discovered the pathognomonic MYD88 L265P mutation and led trials of ibrutinib-based therapy in WM. He has participated in or led more than 200 clinical trials, published over 1,500 peer-reviewed manuscripts with an extraordinary h-index, and serves as past president of the European Myeloma Network and European Hematology Association.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
POLLUX Trial — Daratumumab Plus Rd in Relapsed/Refractory Myeloma
Co-led the phase III POLLUX trial (NEJM 2016; n=569) demonstrating that adding daratumumab to lenalidomide/dexamethasone (D-Rd) significantly improved PFS (median not reached vs. 18.4 months; HR 0.37) and response depth (ORR 93% vs. 76%) versus Rd alone in relapsed/refractory myeloma — resulting in FDA approval and establishing D-Rd as the backbone of relapsed myeloma therapy.
CASTOR Trial — Daratumumab Plus VD Across Multiple Prior Lines
Co-led the phase III CASTOR trial (NEJM 2016; n=498) demonstrating that daratumumab plus bortezomib/dexamethasone (D-VD) significantly improved PFS (median 16.7 vs. 7.1 months; HR 0.31) and MRD negativity versus VD alone in relapsed/refractory myeloma, leading to FDA approval of D-VD and establishing the principle that daratumumab substantially enhances PI- and IMiD-based doublets.
Waldenström Macroglobulinemia — MYD88 Discovery and Ibrutinib Development
Co-discovered the MYD88 L265P somatic mutation present in >90% of WM cases (Nature Genetics 2012), establishing the molecular basis of WM, and subsequently led or co-led clinical trials of ibrutinib in WM (iNNOVATE, ASPEN), establishing ibrutinib-based regimens as standard of care and demonstrating the clinical utility of MYD88/CXCR4 genotyping for therapy selection.
Myeloma Clinical Guidelines and Global Leadership
Served as past president of EHA and the European Myeloma Network; has co-authored IMWG, EHA, and ESMO myeloma clinical guidelines shaping treatment standards across multiple disease settings; contributes to ASCO and ASH educational programs and is among the world's most frequently invited faculty at international hematology meetings.
Representative Works 代表性著作
Daratumumab, Lenalidomide, and Dexamethasone for Multiple Myeloma (POLLUX)
New England Journal of Medicine (2016)
Phase III POLLUX trial establishing daratumumab-Rd as a superior standard to Rd alone for relapsed/refractory myeloma with 63% PFS improvement.
Bortezomib, Dexamethasone, and Daratumumab Versus Bortezomib and Dexamethasone in Relapsed or Refractory Multiple Myeloma (CASTOR)
New England Journal of Medicine (2016)
Phase III CASTOR trial establishing daratumumab-VD as superior to VD in relapsed/refractory myeloma with 69% PFS improvement.
MYD88 L265P somatic mutation in Waldenström's macroglobulinemia
New England Journal of Medicine (2012)
Landmark study identifying MYD88 L265P as the pathognomonic molecular driver of Waldenström macroglobulinemia, transforming diagnosis and therapeutic targeting.
Ibrutinib plus rituximab versus placebo plus rituximab for Waldenström's macroglobulinemia (iNNOVATE)
New England Journal of Medicine (2018)
Phase III iNNOVATE trial establishing ibrutinib-rituximab as standard of care for Waldenström macroglobulinemia.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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