Department of Stem Cell Transplantation and Cellular Therapy, University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
Biol Blood Marrow Transplant. 2010 Aug;16(8):1122-9. doi: 10.1016/j.bbmt.2010.02.015. Epub 2010 Feb 21.
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.
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。