Hematopoietic Cell Transplant and Cell Therapy Program, Massachusetts General Hospital, Boston, Massachusetts.
Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Transplant Cell Ther. 2022 Feb;28(2):109.e1-109.e8. doi: 10.1016/j.jtct.2021.11.002. Epub 2021 Nov 11.
Randomized clinical trials offer the highest-quality data for modifying clinical practice. Results of a phase III randomized trial of nonmyeloablative transplantation for adults with high-risk hematologic malignancies with 2 umbilical cord blood (UCB) units (n = 183) or HLA-haploidentical relative bone marrow (Haplo-BM; n = 154) revealed a 2-year progression-free survival (PFS) of 41% after Haplo-BM transplantation and 35% after 2-unit UCB transplantation (P = .41), with overall survival (OS) of 57% and 46%, respectively (P = .04). We sought to examine the generalizability of BMT CTN 1101 to a contemporaneous cohort beyond the trial's prespecified 2-year outcomes. All transplantations were performed between June 2012 and June 2018 in the United States. We hypothesized that the results of a rigorous phase III randomized trial would be generalizable. Changes in graft selection for HLA-haploidentical relative transplantation during the trial period allowed comparison of outcomes after transplantation with Haplo-BM with those after haploidentical peripheral blood (Haplo-PB). The trial's broad eligibility criteria were applied to the data source of the Center for International Blood and Marrow Transplant Research to select nontrial subjects. Extended follow-up of trial subjects was obtained from this data source. Three separate analyses were performed: (1) trial subjects beyond the trial's 2-year endpoint; (2) comparison of trial subjects with a contemporaneous cohort of nontrial subjects (195 2-unit UCB, 358 Haplo-BM, and 403 Haplo-PB); and (3) comparison of nontrial subjects by donor and graft type. Multivariate analyses were performed using Cox proportional hazards models for comparison of outcomes by treatment groups. With longer follow-up of the trial cohorts, 5-year PFS (37% versus 29%; P = .08) and OS (42% versus 36%; P = .06) were not significantly different between the treatment groups. We then compared the trial results with outcomes of comparable real-world transplantations. Five-year OS did not differ between trial and nontrial 2-unit UCB transplantations (36% versus 41%; P = .48) or between trial and nontrial Haplo-BM transplantations (42% versus 47%; P = .80), confirming generalizability. The randomized trial did not accrue as planned and therefore lacked the statistical power to detect a 15% difference in PFS. With substantially larger numbers of nontrial Haplo-BM transplantations, 5-year survival was higher after nontrial Haplo-BM compared with trial 2-unit UCB (47% versus 36%; P = .012). Nontrial patients who underwent Haplo-PB transplantation had higher 5-year survival (54%) compared with trial Haplo-BM (hazard ratio [HR], 0.76; P = .044) and nontrial Haplo-BM (HR, 0.78; P = .026). Similarly, survival was better after Haplo-PB compared with trial UCB (HR, 0.57; P < .0001) and nontrial UCB (HR, 0.63; P = .0002). When considering alternative donor low-intensity conditioning regimen transplantation, a haploidentical relative is preferred, and PB is the preferred graft source.
随机临床试验为修改临床实践提供了最高质量的数据。一项非清髓性移植治疗高危血液恶性肿瘤的 III 期随机试验的结果显示,183 例接受 2 个脐带血 (UCB) 单位(n = 183)或 HLA 单倍体相合亲缘骨髓 (Haplo-BM; n = 154) 治疗的成人患者,2 年无进展生存率 (PFS) 分别为 Haplo-BM 移植后 41%和 2 单位 UCB 移植后 35%(P =.41),总生存率 (OS) 分别为 57%和 46%(P =.04)。我们试图研究 BMT CTN 1101 在试验规定的 2 年结果之外对当代队列的普遍性。所有移植均于 2012 年 6 月至 2018 年 6 月在美国进行。我们假设严格的 III 期随机试验的结果具有普遍性。试验期间 HLA 单倍体相合亲缘移植的移植物选择的变化允许比较 Haplo-BM 移植后和 Haplo-PB 移植后的结果。该试验的广泛纳入标准适用于国际血液和骨髓移植研究中心的数据来源,以选择非试验对象。从该数据源获得了试验对象的扩展随访数据。进行了三项独立分析:(1) 试验对象超过试验的 2 年终点;(2) 比较试验对象与同时期的非试验对象队列(195 例 2 单位 UCB、358 例 Haplo-BM 和 403 例 Haplo-PB);(3) 按供体和移植物类型比较非试验对象。使用 Cox 比例风险模型进行多变量分析,比较治疗组的结果。随着试验队列的随访时间延长,5 年 PFS(37%比 29%;P =.08)和 OS(42%比 36%;P =.06)在治疗组之间没有显著差异。然后,我们将试验结果与可比真实世界移植的结果进行了比较。5 年 OS 在试验和非试验 2 单位 UCB 移植之间(36%比 41%;P =.48)或试验和非试验 Haplo-BM 移植之间(42%比 47%;P =.80)没有差异,证实了普遍性。该随机试验没有按计划累积,因此缺乏检测 PFS 差异 15%的统计学效力。由于接受非试验 Haplo-BM 移植的人数明显增加,与试验 2 单位 UCB 相比,非试验 Haplo-BM 的 5 年生存率更高(47%比 36%;P =.012)。接受 Haplo-PB 移植的非试验患者的 5 年生存率(54%)高于试验 Haplo-BM(风险比 [HR],0.76;P =.044)和非试验 Haplo-BM(HR,0.78;P =.026)。同样,Haplo-PB 后生存率优于试验 UCB(HR,0.57;P <.0001)和非试验 UCB(HR,0.63;P =.0002)。当考虑替代供体低强度预处理方案移植时,首选单倍体相合亲属,首选 PB 作为移植物来源。