首页> 外文期刊>Journal of Clinical Oncology >Allogeneic stem-cell transplantation in patients with Waldenstrom macroglobulinemia: report from the Lymphoma Working Party of the European Group for Blood and Marrow Transplantation.
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Allogeneic stem-cell transplantation in patients with Waldenstrom macroglobulinemia: report from the Lymphoma Working Party of the European Group for Blood and Marrow Transplantation.

机译:Waldenstrom巨球蛋白血症患者的同种异体干细胞移植:欧洲​​血液和骨髓移植小组淋巴瘤工作组的报告。

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PURPOSE: Allogeneic stem-cell transplantation (alloSCT) is a curative therapeutic option for patients with low-grade lymphoid malignancies. Information regarding alloSCT in Waldenstrom macroglobulinemia (WM) is limited. This study presents the long-term outcome of a large series of patients with WM treated with alloSCT. PATIENTS AND METHODS: A total of 86 patients received allograft by using either myeloablative (MAC; n = 37) or reduced-intensity conditioning (RIC; n = 49) regimens and were retrospectively studied. The median age was 49 years (range, 23 to 64 years); 47 patients had received three or more previous lines of therapy, and eight patients had experienced failure on a prior autologous stem-cell transplantation. A total of 59 patients (68.6%) had chemotherapy-sensitive disease at the time of alloSCT. Median follow-up of the surviving patients was 50 months (7 to 142 months). RESULTS: Nonrelapse mortality (NRM) at 3 years was 33% for MAC and 23% for RIC. The overall response rate was 75.6%. The relapse rates (RRs) at 3 years were 11% for MAC and 25% for RIC. Fourteen patients received donor lymphocyte infusions (DLIs) for disease relapse. PFS and OS at 5 years were 56% and 62% for MAC and 49% and 64% for RIC, respectively. The occurrence of chronic graft-versus-host disease (cGVHD) was associated with a higher NRM and a lower RR, leading to an improvement in PFS. CONCLUSION: alloSCT can induce durable remissions in a selected population of young and heavily pretreated patients with WM. The low RR, the achievement of additional disease responses after DLIs, and the lower RR in patients developing cGVHD suggest the existence of a clinically relevant graft-versus-WM effect.
机译:目的:同种异体干细胞移植(alloSCT)是低度淋巴恶性肿瘤患者的治疗选择。关于Waldenstrom巨球蛋白血症(WM)的alloSCT的信息有限。这项研究显示了用alloSCT治疗的一系列WM患者的长期结果。患者与方法:共有86例患者接受了清髓治疗(MAC; n = 37)或降低强度调节(RIC; n = 49)的同种异体移植,并进行了回顾性研究。中位年龄为49岁(范围为23至64岁); 47名患者曾接受过3种或更多种以前的疗法,而8名患者在先前的自体干细胞移植中经历了失败。在进行alloSCT时,共有59例患者(68.6%)患有化疗敏感性疾病。存活患者的中位随访时间为50个月(7至142个月)。结果:MAC的3年非复发死亡率(NRM)为33%,RIC的为23%。总体回应率为75.6%。 MAC的3年复发率(RRs)为11%,RIC的复发率为25%。 14名患者因疾病复发接受了供体淋巴细胞输注(DLI)。 MAC的5年PFS和OS分别为MAC的56%和62%,RIC的49%和64%。慢性移植物抗宿主病(cGVHD)的发生与较高的NRM和较低的RR相关,从而改善了PFS。结论:alloSCT可以在选定的年轻且经过大量预处理的WM患者中诱导持久缓解。低RR,在DLI后获得额外的疾病反应以及在发生cGVHD的患者中RR较低表明存在临床相关的移植物抗WM效应。

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