Zhang Yumeng, Rose Ashley, Khadka Sushmita, Cao Biwei, Eatrides Jennifer, Saeed Hayder, Shah Bijal D, Chavez Julio, Bello Celeste, Lazaryan Aleksandr, Khimani Farhad, Ibarz Javier Pinilla, Liu Hien D, Locke Frederick L, Jain Michael D, Zhang Ling, Kharfan-Dabaja Mohamed A, Kim Jongphil, Ayala Ernesto, Nishihori Taiga, Sokol Lubomir
Department of Malignant Hematology, Tampa, Florida.
Department of Malignant Hematology, University of Miami Health System, Miami, Florida.
Transplant Cell Ther. 2024 Sep;30(9):887.e1-887.e9. doi: 10.1016/j.jtct.2024.05.006. Epub 2024 May 11.
Nodal peripheral T cell lymphomas (PTCLs) are challenging subsets of non-Hodgkin lymphomas characterized by their heterogeneity and aggressive clinical behavior. Given the mixed outcomes reported in previous studies, the efficacy of autologous hematopoietic cell transplantation (auto-HCT) as a consolidation strategy following initial chemotherapy response remains uncertain. This study aims to evaluate the impact of upfront auto-HCT consolidation on overall survival (OS) and event-free survival (EFS) among patients with nodal PTCL who achieved a complete or partial response to initial chemotherapy. A retrospective cohort study was conducted at Moffitt Cancer Center, involving 123 patients with nodal PTCL treated between February 2005 and February 2021. Patients were stratified into 2 groups based on whether they received auto-HCT as part of their initial treatment strategy. Kaplan-Meier method and Cox proportional hazard models were used for statistical analysis to compare OS and EFS between groups. Patients undergoing auto-HCT after first response demonstrated significantly longer median OS (12.3 versus 4.3 yr; P = .035) and EFS (6.2 versus 2.2 yr; P = .003) compared to those who did not. Multivariate analyses indicated that auto-HCT at first response and younger age at diagnosis were favorable prognostic factors. The findings suggest that upfront auto-HCT consolidation can significantly improve long-term outcomes in patients with nodal PTCL, supporting the strategy of early auto-HCT consideration and referral following initial chemotherapy response. These results underscore the importance of integrating upfront auto-HCT into the treatment paradigm for nodal PTCL, emphasizing early referral to transplantation services to optimize patient outcomes.
结外外周T细胞淋巴瘤(PTCL)是非霍奇金淋巴瘤中具有挑战性的亚型,其特点是具有异质性和侵袭性临床行为。鉴于先前研究报告的结果参差不齐,自体造血细胞移植(auto-HCT)作为初始化疗反应后的巩固策略的疗效仍不确定。本研究旨在评估 upfront auto-HCT 巩固治疗对初始化疗取得完全或部分缓解的结外 PTCL 患者总生存期(OS)和无事件生存期(EFS)的影响。在莫菲特癌症中心进行了一项回顾性队列研究,纳入了2005年2月至2021年2月期间接受治疗的123例结外PTCL患者。根据患者是否接受auto-HCT作为初始治疗策略的一部分将其分为两组。采用Kaplan-Meier法和Cox比例风险模型进行统计分析,比较两组之间的OS和EFS。首次缓解后接受auto-HCT的患者与未接受的患者相比,中位OS(12.3年对4.3年;P = 0.035)和EFS(6.2年对2.2年;P = 0.003)显著更长。多因素分析表明,首次缓解时进行auto-HCT和诊断时年龄较小是有利的预后因素。研究结果表明, upfront auto-HCT巩固治疗可显著改善结外PTCL患者的长期预后,支持在初始化疗反应后早期考虑auto-HCT并转诊的策略。这些结果强调了将 upfront auto-HCT纳入结外PTCL治疗模式的重要性,强调早期转诊至移植服务以优化患者预后。