Reduced-Intensity Allogeneic Hematopoietic Stem Cell Transplantation for Relapsed Multiple Myeloma

被引:29
|
作者
Efebera, Yvonne A. [1 ]
Qureshi, Sofia R. [1 ]
Cole, Suzanne M.
Saliba, Rima [1 ]
Pelosini, Matteo [1 ]
Patel, Ronak M. [1 ]
Koca, Ebru [1 ]
Mendoza, Floralyn L. [1 ]
Wang, Michael
Shah, Jatin
Alousi, Amin [1 ]
Hosing, Chitra [1 ]
Popat, Uday [1 ]
Kebriaei, Partow [1 ]
Anderlini, Paolo [1 ]
Khouri, Issa F. [1 ]
Champlin, Richard [1 ]
Giralt, Sergio [1 ]
Qazilbash, Muzaffar H. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
关键词
Reduce intensity allogeneic transplant; Multiple myeloma; Relapse/refractory; LENALIDOMIDE PLUS DEXAMETHASONE; VERSUS-HOST-DISEASE; AUTOLOGOUS TRANSPLANTATION; PROGNOSTIC-FACTORS; TRIAL; THERAPY; TANDEM; CHEMOTHERAPY; COMBINATION; THALIDOMIDE;
D O I
10.1016/j.bbmt.2010.02.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite recent advances, multiple myeloma (MM) remains incurable, and most patients eventually develop progressive disease. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) offers a potentially curative option in 10%-20% of patients with relapsed or refractory disease. We evaluated the outcome of patients undergoing allo-HSCT with reduced-intensity conditioning (RIC) for relapsed and/or refractory MM at our institution. The study cohort included 51 patients with heavily pretreated, relapsed MM who underwent RIC allo-HSCT between 1996 and 2006. The median time from diagnosis to allo-HSCT was 34 months, and median follow-up in surviving patients was 27 months (range, 3-98 months). Cumulative transplantation-related mortality at 1 year was 25%. Progression-free survival (PFS) and overall survival (OS) at 2 years were 19% and 32%, respectively. The incidences of grade II-IV acute and chronic graft-versus-host disease were 27% and 47%, respectively. At the time of this analysis, 12 patients (24%) were alive, 7 of whom (14%) were in remission for up to 6 years after allo-HSCT. A lower beta 2 microglobulin level (<3.3) and previous autologous HSCT were predictive of lower nonrelapse mortality and longer PFS and OS. Our findings indicate that allo-HSCT with RIC is associated with acceptable toxicity and durable remission and survival in relapsed or refractory MM. The use of RIC allo-HSCT earlier in the course of the disease may offer the greatest benefit. Biol Blood Marrow Transplant 16: 1122-1129 (2010) (C) 2010 American Society for Blood and Marrow Transplantation
引用
收藏
页码:1122 / 1129
页数:8
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