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肿瘤免疫治疗的当前趋势

英文原题:Current trends on immunotherapy for oncology.

查看英文原题

Current trends on immunotherapy for oncology.

PubMed 2025/07/31(内容时间) Bioinformation

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中文摘要

免疫治疗利用患者自身免疫系统识别并清除肿瘤细胞,彻底改变了肿瘤学,并使多种恶性肿瘤获得持久应答。过去十年,靶向CTLA-4、PD-1和PD-L1的免疫检查点抑制剂已成为多种实体瘤的标准治疗,而嵌合抗原受体(CAR)T细胞疗法治疗血液系统恶性肿瘤也显示出显著疗效。尽管取得这些成功,原发性和获得性耐药、免疫相关毒性及治疗成本高等挑战仍限制其更广泛应用。新兴策略包括靶向LAG-3、TIGIT等新型检查点、开发新一代细胞疗法、癌症疫苗和溶瘤病毒,目前均在积极研究,以扩大治疗选择并改善患者结局。开发用于患者筛选的生物标志物,以及将免疫疗法与化疗、靶向药物和放疗联合,对于克服耐药机制至关重要。展望未来,利用肿瘤新抗原和肿瘤微环境的个体化免疫治疗方法,有望带来更精准有效的治疗。

展开英文摘要原文

Immunotherapy has revolutionized oncology by harnessing the patient's own immune system to recognize and eliminate tumor cells, leading to durable responses in a variety of malignancies. Over the past decade, immune checkpoint inhibitors targeting CTLA-4, PD-1, and PD-L1 have become standard of care across multiple solid tumors, while chimeric antigen receptor (CAR) T-cell therapies have demonstrated remarkable efficacy in hematologic cancers. Despite these successes, challenges such as primary and acquired resistance, immune-related toxicities, and high treatment costs continue to limit broader application.

Emerging strategies including novel checkpoint targets ( e. g. , LAG-3, TIGIT), next-generation cellular therapies, cancer vaccines, and oncolytic viruses are under active investigation to expand therapeutic options and improve patient outcomes.

Biomarker development for patient selection and combination regimens with chemotherapy, targeted agents, and radiation are critical to overcoming resistance mechanisms. Looking ahead, personalized immunotherapy approaches leveraging tumor neoantigens and the tumor microenvironment hold promise for more precise and effective treatments.

论文信息

作者
Chander NK、A P、Chandra Ravi P、Muthiah A、Sharma Y、Suriyanarayanan G、P S S
第一作者单位
Institute of Internal Medicine, Madras Medical College & Rajiv Gandhi Government General Hospital, Chennai, India.India
通讯作者单位
Institute of Internal Medicine, Madras Medical College, Chennai, India.India
期刊
Bioinformation2025
原文标识
PubMed 41170078 · DOI 10.6026/973206300211880