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下一代肺癌免疫疗法

英文原题:The next generation of immunotherapies for lung cancers.

PubMed 2025/06/17(内容时间) Nat Rev Clin Oncol Q1 · IF 94.6(JCR 2025)

研究概要

免疫疗法,特别是靶向PD-(L)1或CTLA4的免疫检查点抑制剂(ICIs),已经彻底改变了肺癌的治疗;

中文摘要

免疫疗法,特别是靶向PD-(L)1或CTLA4的免疫检查点抑制剂(ICIs),已经彻底改变了肺癌的治疗格局;然而,许多患者对ICIs无应答,而大多数初始肿瘤有应答的患者最终因获得性耐药而出现疾病进展。在过去几年中,人们探索了大量治疗策略来解决ICIs原发性和获得性耐药的问题。2024年,双特异性PD-1 × VEGF抗体ivonescimab在中国获批用于治疗非小细胞肺癌,以及双特异性DLL3 × CD3 T细胞衔接器tarlatamab在美国获批用于小细胞肺癌患者,为利用新型免疫治疗药物克服ICI耐药挑战提供了临床概念验证,从而增强了探索下一代肺癌免疫疗法的热情。目前,大量具有不同靶点和作用机制的免疫疗法正在涉及肺癌患者的临床试验中进行测试。在本综述中,我们概述了这些正在临床开发中用于非小细胞肺癌和/或小细胞肺癌的新兴免疫疗法,包括新型免疫检查点调节剂、免疫细胞衔接器、过继性细胞疗法和治疗性癌症疫苗。我们描述了这些药物的设计以及它们可能克服对当前一代ICIs耐药的机制。我们还讨论了阻碍每种免疫治疗模态临床转化的障碍以及应对这些挑战的潜在策略,并使用了已进入后期临床测试阶段的代表性药物作为示例。

展开英文摘要原文

Immunotherapies, specifically immune-checkpoint inhibitors (ICIs) targeting PD-(L)1 or CTLA4, have revolutionized the treatment of lung cancer; however, many patients do not have a response to ICIs and most of those with an initial tumour response eventually have disease progression owing to acquired resistance. Over the past few years, numerous therapeutic strategies have been explored to address the problems of intrinsic and acquired resistance to ICIs. In 2024, regulatory approvals of the bispecific PD-1 × VEGF antibody ivonescimab for the treatment of non-small-cell lung cancer in China and the bispecific DLL3 × CD3 T cell engager tarlatamab for patients with small cell lung cancer in the USA provided clinical proof-of-concept for overcoming the challenge of ICI resistance using novel immunotherapeutic agents, thereby increasing enthusiasm for the exploration of next-generation immunotherapies for lung cancer. A large variety of immunotherapies with diverse targets and mechanisms of action are currently being tested in clinical trials involving patients with lung cancer. In this Review, we provide an overview of these emerging immunotherapies in clinical development for non-small-cell lung cancer and/or small cell lung cancer, including novel immune-checkpoint modulators, immune cell engagers, adoptive cell therapies and therapeutic cancer vaccines. We describe the designs of these agents and the mechanisms by which they might overcome resistance to the current generation of ICIs. We also discuss hurdles impeding the clinical translation of each immunotherapeutic modality and potential strategies to address these challenges, using representative examples of agents that have entered the later phases of clinical testing.

论文信息

作者
Zhao S、Zhao H、Yang W、Zhang L
第一作者单位
Department of Medical Oncology, Sun Yat-sen University Cancer Centre, State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Guangdong Provincial Clinical Research Centre for Cancer, Guangzhou, China.China
通讯作者单位
Department of Medical Oncology, Sun Yat-sen University Cancer Centre, State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Guangdong Provincial Clinical Research Centre for Cancer, Guangzhou, China. zhangli@sysucc.org.cn.China
文献类型
综述
期刊
Nature reviews. Clinical oncology2025 Aug
原文标识
PubMed 40528044 · DOI 10.1038/s41571-025-01035-9