Division of Hematology and Oncology, Department of Medicine A, Muenster University Hospital, Muenster, Germany.
Department of Hematology and Oncology, Georg August University Goettingen, Goettingen, Germany.
Blood. 2021 May 13;137(19):2646-2656. doi: 10.1182/blood.2020008825.
First-line therapy for younger patients with peripheral T-cell non-Hodgkin lymphoma (T-NHL) consists of 6 courses of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) with or without etoposide (CHOEP), consolidated by high-dose therapy and autologous stem cell transplantation (auto-SCT). We hypothesized that allogeneic stem cell transplantation (allo-SCT) could improve outcomes. 104 patients with peripheral T-cell non-Hodgkin lymphoma, except ALK+ anaplastic large cell lymphoma, 18 to 60 years, all stages, and all age adjusted International Prognostic Index scores, except 0 and stage I, were randomized to 4 cycles of CHOEP and 1 cycle of dexamethasone, cytosine-arabinoside, and platinum (DHAP) followed by high-dose therapy and auto-SCT or myeloablative conditioning and allo-SCT. The primary end point was event-free survival (EFS) at 3 years. After a median follow-up of 42 months, the 3-year EFS after allo-SCT was 43%, as compared with 38% after auto-SCT. Overall survival at 3 years was 57% vs 70% after allo- or auto-SCT, without significant differences between treatment arms. None of the 21 responding patients proceeding to allo-SCT relapsed, as opposed to 13 of 36 patients (36%) proceeding to auto-SCT. Eight of 26 patients (31%) and none of 41 patients died of transplant-related toxicity after allo- and auto-SCT, respectively. The strong graft-versus-lymphoma effect after allo-SCT was counterbalanced by transplant-related mortality. This trial is registered at www.clinicaltrials.gov as #NCT00984412.
对于年轻的外周 T 细胞非霍奇金淋巴瘤(T-NHL)患者,一线治疗包括 6 个疗程的环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP),加或不加依托泊苷(CHOEP),巩固治疗采用大剂量化疗和自体干细胞移植(auto-SCT)。我们假设异基因干细胞移植(allo-SCT)可以改善预后。104 例外周 T 细胞非霍奇金淋巴瘤患者,ALK+间变性大细胞淋巴瘤除外,年龄 18 至 60 岁,所有分期,除 0 期和 I 期外,所有年龄调整的国际预后指数评分,随机分为 4 个周期的 CHOEP 和 1 个周期的地塞米松、阿糖胞苷和铂(DHAP),然后进行大剂量化疗和自体 SCT 或清髓性预处理和 allo-SCT。主要终点是 3 年无事件生存(EFS)。中位随访 42 个月后,allo-SCT 后 3 年的 EFS 为 43%,而自体 SCT 后为 38%。3 年总生存率在 allo-SCT 组为 57%,自体 SCT 组为 70%,两组之间无显著差异。21 例allo-SCT 后缓解的患者中无 1 例复发,而 36 例自体 SCT 后缓解的患者中有 13 例(36%)复发。allo-SCT 和 auto-SCT 后分别有 8 例(31%)和 41 例(0%)患者死于移植相关毒性,无统计学差异。allo-SCT 后强烈的移植物抗淋巴瘤效应被移植相关死亡率所抵消。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT00984412。