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前瞻性随机 AATT 研究(自体或异体移植治疗外周 T 细胞淋巴瘤)的长期随访。

Long-Term Follow-Up of the Prospective Randomized AATT Study (Autologous or Allogeneic Transplantation in Patients With Peripheral T-Cell Lymphoma).

机构信息

Service d'Hématologie Clinique et de Thérapie Cellulaire, CHU Estaing, EA7453 CHELTER and CIC-1405, Université Clermont Auvergne, Clermont-Ferrand, France.

Institute for Medical Informatics, Statistics, and Epidemiology, University Leipzig, Leipzig, Germany.

出版信息

J Clin Oncol. 2024 Nov 10;42(32):3788-3794. doi: 10.1200/JCO.24.00554. Epub 2024 Sep 13.

Abstract

JCO Primary analysis of the phase III randomized AATT study showed that younger patients with peripheral T-cell lymphoma (PTCL) consolidated with autologous or allogeneic transplantation (alloSCT) had similar event-free survival (EFS) and overall survival (OS). Seven-year EFS of patients randomly assigned to alloSCT was 38% (95% CI, 25 to 52) compared with 34% (95% CI, 22 to 47) for patients randomly assigned to autologous transplantation of hematopoietic stem cells (autoSCT); OS was 55% (95% CI, 41 to 69) and 61% (95% CI, 47 to 74). Among patients undergoing alloSCT (n = 26) or autoSCT (n = 41) on study, the cumulative progression/relapse rate was 8% (95% CI, 0 to 19) and 55% (95% CI, 35 to 74). Nonrelapse mortality (NRM) was 31% (95% CI, 13 to 49) and 3% (95% CI, 0 to 8) after alloSCT and autoSCT, respectively. Fifteen of 30 patients with early progression and 11 of 20 patients with progression/relapse after autoSCT received alloSCT. Seven-year OS after salvage alloSCT was 61% (95% CI, 47 to 74); NRM was 23% (95% CI, 6 to 40). Long-term follow-up documents the strong graft versus lymphoma effect of alloSCT independent of the timing of transplantation. Survival of patients unable to undergo transplantation was dismal. AlloSCT is the treatment of choice for younger, transplant-eligible patients with relapsed/refractory PTCL. AlloSCT is currently not recommended as part of first-line consolidation.

摘要

JCO 三期随机 AATT 研究的主要分析显示,年轻的外周 T 细胞淋巴瘤(PTCL)患者巩固自体或异基因移植(alloSCT)后,无事件生存(EFS)和总生存(OS)相似。随机分配到 alloSCT 的患者 7 年 EFS 为 38%(95%CI,25 至 52),而随机分配到自体造血干细胞移植(autoSCT)的患者为 34%(95%CI,22 至 47);OS 为 55%(95%CI,41 至 69)和 61%(95%CI,47 至 74)。在接受 alloSCT(n=26)或 autoSCT(n=41)的患者中,累积进展/复发率分别为 8%(95%CI,0 至 19)和 55%(95%CI,35 至 74)。alloSCT 和 autoSCT 后非复发死亡率(NRM)分别为 31%(95%CI,13 至 49)和 3%(95%CI,0 至 8)。15 例早期进展患者和 20 例 autoSCT 后进展/复发患者中的 11 例接受 alloSCT。挽救性 alloSCT 后 7 年 OS 为 61%(95%CI,47 至 74);NRM 为 23%(95%CI,6 至 40)。长期随访证明 alloSCT 具有强大的移植物抗淋巴瘤效应,与移植时机无关。无法进行移植的患者的生存情况较差。alloSCT 是年轻、适合移植的复发/难治性 PTCL 患者的治疗选择。alloSCT 目前不建议作为一线巩固治疗的一部分。

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