Reduced-intensity allogeneic hematopoietic stem cell transplantation for relapsed multiple myeloma.
Reduced-intensity allogeneic hematopoietic stem cell transplantation for relapsed multiple myeloma.
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DOI:
10.1016/j.bbmt.2010.02.015
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发表时间:
2010-08
影响因子:
4.3
通讯作者:
Qazilbash, Muzaffar H.
中科院分区:
文献类型:
--
作者:
Efebera, Yvonne A.;Qureshi, Sofia R.;Cole, Suzanne M.;Saliba, Rima;Pelosini, Matteo;Patel, Ronak M.;Koca, Ebru;Mendoza, Floralyn L.;Wang, Michael;Shah, Jatin;Alousi, Amin;Hosing, Chitra;Popat, Uday;Kebriaei, Partow;Anderlini, Paolo;Khouri, Issa F.;Champlin, Richard;Giralt, Sergio;Qazilbash, Muzaffar H.
Despite recent advances, multiple myeloma remains incurable and most patients eventually develop progressive disease. Allogeneic hematopoietic stem cell transplantation (allo HCT) offers a potentially curative option in 10–20% of patients with relapsed or refractory disease. We evaluated the outcome of patients undergoing allo HCT with reduced-intensity conditioning (RIC) for relapsed and/or refractory myeloma at our institution. Fifty-one patients with heavily pretreated, relapsed myeloma, who received RIC allo HCT between 1996 and 2006, were included in this analysis. Median time from diagnosis to allo HCT was 34 months. Median follow-up in surviving patients was 27 months (3–98). Cumulative transplant-related mortality (TRM) at 1 year was 25%. Progression-free survival (PFS) and overall survival (OS) at 2 years were 19% and 32%, respectively. The incidence of grade II-IV acute or chronic graft-vs-host disease (GVHD) was 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 SCT. A lower β2 microglobulin (<3.3) and a prior autotransplant predicted a lower NRM, longer PFS and OS. Allo HCT with RIC regimens is associated with acceptable toxicity and durable remission and survival in relapsed or refractory myeloma. Use of RIC allo HCT earlier in the course of the disease may offer greater benefit.
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影响因子:
20.3
作者:
Kröger, N;Sayer, HG;Zander, AR
通讯作者:
Zander, AR
影响因子:
10.3
作者:
Kumar, Ambuj;Kharfan-Dabaja, Mohamed A.;Djulbegovic, Benjamin
通讯作者:
Djulbegovic, Benjamin
影响因子:
45.3
作者:
Barlogie, B;Kyle, RA;Crowley, JC
通讯作者:
Crowley, JC
影响因子:
158.5
作者:
Bruno, Benedetto;Rotta, Marcello;Boccadoro, Mario
通讯作者:
Boccadoro, Mario
影响因子:
4.8
作者:
de Lavallade, H.;El-Cheikh, J.;Mohty, M.
通讯作者:
Mohty, M.