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降低强度异基因造血干细胞移植治疗复发性多发性骨髓瘤。

Reduced-intensity allogeneic hematopoietic stem cell transplantation for relapsed multiple myeloma.

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Aug;16(8):1122-9. doi: 10.1016/j.bbmt.2010.02.015. Epub 2010 Feb 21.

Abstract

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 beta2 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.

摘要

尽管最近取得了进展,但多发性骨髓瘤(MM)仍然无法治愈,大多数患者最终会发展为进行性疾病。异基因造血干细胞移植(allo-HSCT)为 10%-20%的复发或难治性疾病患者提供了一种潜在的治愈选择。我们评估了我们机构中接受减轻强度预处理(RIC)的复发和/或难治性 MM 患者进行 allo-HSCT 的结果。研究队列包括 51 名接受过大量预处理、复发 MM 的患者,他们在 1996 年至 2006 年间接受了 RIC allo-HSCT。从诊断到 allo-HSCT 的中位时间为 34 个月,存活患者的中位随访时间为 27 个月(范围 3-98 个月)。1 年时累积移植相关死亡率为 25%。2 年时无进展生存期(PFS)和总生存期(OS)分别为 19%和 32%。急性和慢性移植物抗宿主病的发生率分别为 27%和 47%。在本分析时,12 名患者(24%)存活,其中 7 名(14%)在 allo-HSCT 后长达 6 年仍处于缓解状态。较低的β2 微球蛋白水平(<3.3)和先前的自体 HSCT 是较低的非复发死亡率和更长的 PFS 和 OS 的预测因素。我们的研究结果表明,RIC allo-HSCT 与可接受的毒性和复发性或难治性 MM 的持久缓解和生存相关。在疾病早期使用 RIC allo-HSCT 可能会带来最大的益处。

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