Craig H. Moskowitz
克雷格·莫斯科维茨
MD
Division Chief, Hematology; Professor of Medicine, University of Miami Miller School of Medicine血液学部主任;迈阿密大学米勒医学院医学教授
👥Biography 个人简介
Craig H. Moskowitz, MD is Division Chief of Hematology and Professor of Medicine at the Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine. He is one of the most prominent clinical investigators in Hodgkin lymphoma (HL) globally, known for leading the ECHELON-1 trial — a phase III randomized study published in NEJM (2018) comparing brentuximab vedotin plus AVD (A+AVD) with standard ABVD chemotherapy in previously untreated advanced classical Hodgkin lymphoma. ECHELON-1 demonstrated that A+AVD significantly improved modified progression-free survival compared with ABVD, leading to FDA and EMA approval of A+AVD as a preferred frontline regimen for advanced HL and representing the first phase III improvement over ABVD in over three decades. Prior to ECHELON-1, Dr. Moskowitz made foundational contributions to salvage chemotherapy strategies in relapsed/refractory HL, including the development and validation of ICE (ifosfamide, carboplatin, etoposide) chemotherapy and the application of PET-adapted therapy to guide transplant eligibility decisions. He has also been a leading investigator in clinical trials of pembrolizumab in relapsed/refractory classical HL (KEYNOTE-204) and in the design of novel transplant consolidation strategies. Dr. Moskowitz formerly directed the Lymphoma Service at MSK for many years before joining Sylvester.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
ECHELON-1 Trial — A+AVD as New Frontline Standard for Advanced Hodgkin Lymphoma
Led the phase III ECHELON-1 trial (NEJM 2018) demonstrating that brentuximab vedotin plus AVD (A+AVD) improved modified PFS (HR 0.77) and long-term OS compared with ABVD in previously untreated advanced classical Hodgkin lymphoma, achieving FDA and EMA approval and establishing A+AVD as a preferred frontline option — the first survival improvement over ABVD shown in a randomized phase III trial for over 30 years.
ICE Salvage Chemotherapy and ASCT Strategy in Relapsed/Refractory HL
Developed and validated the ICE (ifosfamide, carboplatin, etoposide) salvage chemotherapy regimen at MSK as a standard pre-transplant mobilization approach in relapsed/refractory Hodgkin lymphoma, and led analyses using PET response after ICE to select patients most likely to benefit from high-dose therapy and autologous stem cell transplantation — defining a PET-adapted salvage framework widely adopted internationally.
PD-1 Blockade in Classical Hodgkin Lymphoma
Was a leading investigator in KEYNOTE-204, the phase III trial comparing pembrolizumab with brentuximab vedotin in relapsed/refractory classical HL, demonstrating superior PFS and response rates with pembrolizumab in patients failing ASCT or ineligible for transplant, and contributing to the approval of pembrolizumab in third-line+ HL.
Brentuximab Vedotin Post-Transplant Consolidation
Led the AETHERA trial, a randomized phase III study demonstrating that brentuximab vedotin as consolidation therapy following autologous stem cell transplantation significantly improved PFS in high-risk relapsed/refractory classical Hodgkin lymphoma, establishing brentuximab post-ASCT maintenance as a standard of care.
Representative Works 代表性著作
Brentuximab Vedotin with Chemotherapy for Stage III or IV Hodgkin's Lymphoma (ECHELON-1)
New England Journal of Medicine (2018)
Phase III ECHELON-1 trial demonstrating A+AVD superiority over ABVD in advanced Hodgkin lymphoma, establishing a new frontline standard for the first time in three decades.
Brentuximab vedotin as consolidation therapy after autologous stem-cell transplantation in patients with Hodgkin's lymphoma at risk of relapse or progression (AETHERA)
The Lancet (2015)
Phase III AETHERA trial establishing brentuximab vedotin post-ASCT maintenance as standard of care for high-risk relapsed/refractory Hodgkin lymphoma.
Pembrolizumab versus brentuximab vedotin in relapsed or refractory classical Hodgkin lymphoma (KEYNOTE-204)
Lancet Oncology (2021)
Phase III KEYNOTE-204 trial demonstrating superior PFS with pembrolizumab versus brentuximab vedotin in relapsed/refractory classical Hodgkin lymphoma after ASCT failure.
High-dose chemoradiotherapy and stem-cell rescue for patients with relapsed seminoma
Journal of Clinical Oncology (2001)
ICE chemotherapy regimen validation study at MSK demonstrating efficacy as salvage and mobilization therapy prior to ASCT in relapsed lymphoma and germ cell tumors.
🏆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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