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复发/难治性结外自然杀伤/T 细胞淋巴瘤的机制与干预

英文原题:Mechanisms and interventions in relapsed/refractory extranodal natural killer/T-cell lymphoma.

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Mechanisms and interventions in relapsed/refractory extranodal natural killer/T-cell lymphoma.

PubMed 2025/11/18(内容时间) Drug Discov Today Q1 · IF 8.7(JCR 2025)

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中文摘要

结外自然杀伤/T细胞淋巴瘤(ENKTL)是一种与Epstein-Barr病毒相关的侵袭性非霍奇金淋巴瘤,通常累及结外部位。传统的CHOP方案由于耐药已不再是标准治疗,而基于门冬酰胺酶的疗法已成为主要治疗手段。然而,耐药和肿瘤侵袭导致40-50%的患者复发,其中20%进展为复发/难治性ENKTL,中位生存期<12个月。ENKTL的管理仍然具有挑战性,存在未满足的临床需求。然而,尽管复发/难治性ENKTL的预后较差,但随着对该疾病认识的深入,新的治疗策略正在不断发展。本综述探讨了导致治疗耐药的因素、潜在的耐药机制以及克服ENKTL耐药的潜在策略。

展开英文摘要原文

Extranodal natural killer/T-cell lymphoma (ENKTL) is an aggressive non-Hodgkin's lymphoma associated with Epstein-Barr virus and typically involves extranodal sites. The traditional CHOP regimen is no longer standard owing to drug resistance, whereas asparaginase-based therapies have become the mainstay of treatment.

However, resistance and tumor invasion lead to relapses in 40-50% of patients, with 20% progressing to relapsed/refractory ENKTL, resulting in a median survival of <12 months. Management of ENKTL remains challenging, with an unmet clinical need.

However, although the prognosis for relapsed/refractory ENKTL is poor, the development of new treatment strategies is progressing with a better understanding of the disease. This review examines factors contributing to treatment resistance, underlying resistance mechanisms and potential strategies to overcome ENKTL resistance.

论文信息

作者
Lu Q、You T、Cheng Q、Chen ZS、Huang H
第一作者单位
National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China; Department of Hematology, Foresea Life Insurance Guangzhou General Hospital, Guangzhou, China.China
通讯作者单位
National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China. Electronic address: huanghaiwen@suda.edu.cn.China
文献类型
综述
期刊
Drug discovery today2025 Dec
原文标识
PubMed 41265515 · DOI 10.1016/j.drudis.2025.104549