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弥漫性大 B 细胞淋巴瘤:过去 5 年我们看到了哪些临床进展?

英文原题:Diffuse large B-cell lymphoma: what clinical progress have we seen in the last 5 years?

查看英文原题

Diffuse large B-cell lymphoma: what clinical progress have we seen in the last 5 years?

PubMed 2025/11/24(内容时间) Expert Opin Investig Drugs Q2 · IF 4.3(JCR 2025)

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研究概要

在现代 DLBCL 治疗中,识别 R-CHOP 原发治疗失败风险增加的个体至关重要,这些患者随后可能在一线治疗中接受 Polatuzumab Vedotin 或其他靶向治疗的添加。CAR-T 现已成为原发难治或早期复发疾病患者二线治疗的标准,ASCT 则保留给适合的晚期复发患者,这些患者随后可能在第三线接受 CAR-T。不适合 ASCT 的患者也因 CAR-T 和包含新型药物的增强治疗而面临改善的结局。未来,分子和基因组肿瘤分析可能通过识别对不同靶向药物敏感的生物学上不同的淋巴瘤,来指导患者的最佳治疗。

研究思路结论见上方概要

弥漫性大B细胞淋巴瘤是非霍奇金淋巴瘤最常见的亚型,其治疗格局正在迅速演变。对于原发治疗失败风险增加的患者以及复发/难治性疾病的患者,新兴的治疗类别已显著改善了结局。涵盖领域:本综述描述了评估DLBCL一线治疗以及适合强化治疗和不适合强化治疗患者的复发/难治性治疗中最重要的试验。特别关注CAR-T、双特异性抗体和分子靶向治疗的合理治疗排序和选择。

展开英文摘要原文

INTRODUCTION: Diffuse large B-cell lymphoma is the most common subtype of non-Hodgkin lymphoma and has a rapidly evolving treatment landscape. For patients at increased risk of primary treatment failure and those with relapsed/refractory disease, emerging therapeutic classes have significantly improved outcomes. AREAS COVERED: This review describes the most important trials evaluating treatment for DLBCL in frontline and the relapsed/refractory setting for both fit patients and patients ineligible for intensive therapy. Particular attention is paid to rational treatment sequencing and selection for CAR-T, bispecific antibodies and molecularly targeted therapies.

EXPERT OPINION: In modern DLBCL therapy, it is critical to identify individuals at increased risk of primary treatment failure with R-CHOP, who may then be offered the addition of Polatuzumab Vedotin or other targeted therapies in frontline. CAR-T is now a treatment standard in second line for patients with primary refractory or early relapsed disease, with ASCT reserved for eligible patients with later relapse, who may subsequently receive CAR-T in third-line.

ASCT ineligible patients also face improved outcomes with CAR-T and enhanced therapies incorporating novel agents. Molecular and genomic tumor profiling is likely in the future to direct optimal treatment for patients by identifying biologically distinct lymphomas sensitive to distinct targeted agents.

论文信息

作者
Nolan J、Kuruvilla J
单位
Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.Canada
文献类型
综述
期刊
Expert opinion on investigational drugs2025 Nov
原文标识
PubMed 41204727 · DOI 10.1080/13543784.2025.2587276