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一项自体与异体移植作为一线治疗不良预后外周 T-NHL 方案的随机 3 期临床试验。

A randomized phase 3 trial of autologous vs allogeneic transplantation as part of first-line therapy in poor-risk peripheral T-NHL.

机构信息

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.

出版信息

Blood. 2021 May 13;137(19):2646-2656. doi: 10.1182/blood.2020008825.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93d9/9635528/805dfe1c78f7/bloodBLD2020008825absf1.jpg

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