新诊断的晚期结外自然杀伤/ T细胞淋巴瘤的治疗和预后:一项跨越二十年的单中心真实世界研究

IF 2 4区 医学 Q3 ONCOLOGY
Chemotherapy Pub Date : 2024-01-01 Epub Date: 2023-11-20 DOI:10.1159/000535128
Yu-Ce Wei, Fei Qi, Bo Chen, Chang-Gong Zhang, Hui Fang, Di Zhang, Shu-Nan Qi, Yue Chai, Ye-Xiong Li, Mei Dong
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引用次数: 0

摘要

导论:虽然目前以天冬酰胺酶为基础的化疗方案治疗晚期结外自然杀伤/ T细胞淋巴瘤(ENKTCLs)已经有了共识,但根据以往的文献报道,患者在现实环境中的生存情况仍然不容乐观,在联合治疗理念下的最佳化疗方案和不同治疗方法的整合仍需要进一步探索和验证。方法:回顾性收集近二十年来中国癌症中心新确诊的Ⅲ/Ⅳ期ENKTCL患者资料进行分析。总生存期(OS)和无进展生存期(PFS)作为主要终点。采用Log-rank检验和Cox比例风险模型来检验亚组间的生存差异,并检验单变量和多变量的关联。结果:该研究纳入83例新诊断的Ⅲ/Ⅳ期ENKTCL患者,中位OS为26.07个月,估计5年OS为41.3%,中位随访时间为82.13个月。一线天冬酰胺酶-与非天冬酰胺酶方案相比,显著延长PFS (P=0.007;HR=0.48, P=0.020),有改善OS的趋势(P=0.064;HR = 0.74, P = 0.359)。以吉西他滨为基础的方案也显示出改善PFS的趋势(P=0.048;HR=0.59, P=0.164)和OS (P=0.008;HR=0.67, P=0.282)。天冬酰胺酶和吉西他滨联合治疗的5年OS为55.0%,PFS显著优于对照组(P=0.020;HR=0.40, P=0.022), OS稍好(P=0.054;HR=0.79, P=0.495)。与单纯化疗相比,一线放化疗联合治疗提高了PFS (P=0.051)和OS (P=0.036)。4例自体造血干细胞移植受者的中位生存期为58.34个月。结论:天冬酰胺酶联合吉西他滨对PFS和OS有较好的影响;天冬酰胺酶联合吉西他滨化疗的疗效、缓解时间和生存期均最佳。联合治疗包括强效化疗辅以放疗和/或巩固性移植可以改善新诊断的晚期enktcl的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment and Prognosis of Newly Diagnosed Advanced-Stage Extranodal Natural Killer/T-Cell Lymphoma: A Single-Center Real-World Study across Two Decades.

Introduction: Although there is now a consensus on asparaginase-based chemotherapy regimens in the treatment of advanced-stage extranodal natural killer/T-cell lymphomas (ENKTCLs), patient survival in the real-world setting is still not optimistic according to previous literature reports, and the optimal chemotherapeutic regimens and integration of different therapeutic methods under the concept of combined-modality treatment still need to be further explored and verified.

Methods: Newly diagnosed stage Ⅲ/Ⅳ ENKTCL patients from Chinese National Cancer Center in the last two decades were retrospectively collected and analyzed. Overall survival (OS) and progression-free survival (PFS) were determined as primary endpoints. Log-rank tests and Cox proportional hazard models were performed to test for survival differences between subgroups and examine the univariable and multivariable associations.

Results: The study included 83 newly diagnosed stage Ⅲ/Ⅳ ENKTCL patients and reported a median OS of 26.07 months and an estimated 5-year OS of 41.3% with a median follow-up of 82.13 months. First-line asparaginase-based regimens compared to non-asparaginase-based regimens significantly prolonged PFS (p = 0.007; HR = 0.48, p = 0.020) and showed a tendency to improve OS (p = 0.064; HR = 0.74, p = 0.359). Gemcitabine-based regimens also exhibited a trend toward improved PFS (p = 0.048; HR = 0.59, p = 0.164) and OS (p = 0.008; HR = 0.67, p = 0.282) compared to non-gemcitabine-based ones. The asparaginase and gemcitabine combinations yielded a 5-year OS of 55.0% and led to significantly superior PFS (p = 0.020; HR = 0.40, p = 0.022) and slightly better OS (p = 0.054; HR = 0.79, p = 0.495) compared to the remaining regimens. First-line combined-modality treatment integrating chemotherapy and radiotherapy improved PFS (p = 0.051) and OS (p = 0.036) compared to chemotherapy alone. Four autologous hematopoietic stem cell transplantation recipients reached a median OS of 58.34 months.

Conclusion: Asparaginase and gemcitabine alone brought a favorable impact on PFS and OS; and the asparaginase and gemcitabine combination chemotherapy yielded the optimal efficacy, response duration, and survival outcomes. Combined-modality treatment including potent chemotherapy supplemented by radiotherapy and/or consolidative transplantation could improve prognosis in newly diagnosed advanced-stage ENKTCLs.

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来源期刊
Chemotherapy
Chemotherapy 医学-药学
CiteScore
5.80
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: This journal publishes original research articles and state-of-the-art reviews on all aspects of antimicrobial and antitumor chemotherapy. The results of experimental and clinical investigations into the microbiological and pharmacologic properties of antibacterial, antiviral and antitumor compounds are major topics of publication. Papers selected for the journal offer data concerning the efficacy, toxicology, and interactions of new drugs in single or combined applications. Studies designed to determine the pharmacokinetic and pharmacodynamics properties of similar preparations and comparing their efficacy are also included. Special emphasis is given to the development of drug-resistance, an increasing problem worldwide.
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