Department of Hematology & Bone Marrow Transplantation, Ramban Medical Center, Haifa, Israel.
Clinical Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Bone Marrow Transplant. 2014 May;49(5):671-8. doi: 10.1038/bmt.2014.4. Epub 2014 Feb 10.
The objective of this retrospective analysis was to compare outcomes of patients with diffuse large B-cell lymphoma (DLBCL) who received either a matched sibling (sib) or an unrelated donor (URD) allogeneic hematopoietic cell transplantation (allo-HCT). Long-term outcome of 172 DLBCL patients receiving URD-HCT between 2000 and 2007 and reported to the European Group for Blood and Marrow Transplantation, was compared with that of 301 subjects, allografted from sib-HCT. With a median follow-up of 45 months, 3-year PFS approached 35% for both groups; overall survival (OS) was 42% for sib-HCT versus 37% for URD (NS). Multivariate analyses confirmed that donor type was not associated with differences in non-relapse mortality (NRM), relapse rate (RR), PFS or OS. Poor performance status (PS) and refractory disease adversely affected PFS and OS. Prior auto-SCT and multiple previous therapies predicted for shorter PFS. NRM was adversely affected by older age (⩾50 years), poor PS and refractory disease, and RR by time from diagnosis to allo-HCT of <36 months, prior auto-SCT, refractory disease, poor PS and in vivo T-cell depletion with alemtuzumab. This large study shows for the first time that URD-HCT is not inferior to sib-HCT, providing a reasonable therapeutic approach for DLBCL patients, having no HLA-identical sibling available.
本回顾性分析旨在比较接受匹配的同胞供体(sib)或无关供体(URD)异基因造血细胞移植(allo-HCT)的弥漫性大 B 细胞淋巴瘤(DLBCL)患者的结局。比较了 2000 年至 2007 年间接受 URD-HCT 的 172 例 DLBCL 患者和向欧洲血液和骨髓移植协会报告的 301 例接受 sib-HCT 的患者的长期结局。中位随访 45 个月,两组 3 年无进展生存率(PFS)均接近 35%;总体生存率(OS)为 sib-HCT 组 42%,URD 组 37%(NS)。多变量分析证实供体类型与非复发死亡率(NRM)、复发率(RR)、PFS 或 OS 无差异。一般状况差(PS)和难治性疾病对 PFS 和 OS 产生不利影响。既往自体-SCT 和多次先前治疗与较短的 PFS 相关。NRM 受年龄较大(≥50 岁)、PS 差和难治性疾病、RR 受从诊断到 allo-HCT 的时间<36 个月、既往自体-SCT、难治性疾病、PS 差和用阿仑单抗进行体内 T 细胞耗竭的影响。这项大型研究首次表明 URD-HCT 并不逊于 sib-HCT,为没有 HLA 完全匹配的同胞供体的 DLBCL 患者提供了一种合理的治疗方法。