Suppr超能文献

肿瘤免疫治疗协会观点:利用患者富集生物标志物加速免疫肿瘤学早期药物研发

SITC perspective: leveraging patient enrichment biomarkers to accelerate early phase IO drug development.

作者信息

Emens Leisha A, Moussion Christine, Hwu Patrick, Gulley James L, Ohashi Pamela S, Bifulco Carlo B, Feltquate David

机构信息

Kaiser Permanente, South Sacramento, California, USA

Genentech, South San Francisco, California, USA.

出版信息

J Immunother Cancer. 2025 Jun 22;13(6):e010739. doi: 10.1136/jitc-2024-010739.

Abstract

Cancer immunotherapy (IO) enables patients to live well with cancer for many years, or even be cured. Several investigational IO agents recently failed in early-phase or late-phase trials, leading some to doubt the future of IO. Patient heterogeneity (eg, tumor characteristics, treatment history) increases the risk that a clinically active IO drug might be discarded. Enriching enrollment for patients with biomarkers hypothesized to reflect a higher probability of clinical benefit across clinical development should mitigate this risk. The Society for Immunotherapy of Cancer convened diverse IO stakeholders to discuss leveraging biomarkers at the earliest stages of drug development to accelerate the delivery of innovative IO agents to patients. This group developed a framework based on a biomarker-based enrichment strategy in early trials that evolves into the development of more precise predictive biomarkers in late phase trials. This framework integrates mechanistic insights related to the drug and its impact on the tumor microenvironment derived from preclinical data, digital pathology, exploratory multiomics, and artificial intelligence that are continuously refined through both adaptive and randomized clinical trials. Biomarker-based enrichment in early clinical development should de-risk late-stage trials, ultimately expanding the portfolio of innovative IO drugs available to patients.

摘要

癌症免疫疗法(IO)使患者能够与癌症长期共存,甚至实现治愈。近期,几种处于研究阶段的IO药物在早期或晚期试验中失败,这使得一些人对IO的未来产生怀疑。患者的异质性(如肿瘤特征、治疗史)增加了临床活性IO药物可能被弃用的风险。在临床开发过程中,为那些被认为更有可能从生物标志物中获得临床益处的患者增加入组人数,应可降低这一风险。癌症免疫治疗协会召集了不同的IO利益相关者,讨论如何在药物开发的最早阶段利用生物标志物,以加速将创新的IO药物提供给患者。该小组制定了一个框架,基于早期试验中基于生物标志物的富集策略,在后期试验中演变为开发更精确的预测性生物标志物。该框架整合了与药物及其对肿瘤微环境影响相关的机制见解,这些见解源自临床前数据、数字病理学、探索性多组学和人工智能,并通过适应性和随机临床试验不断完善。早期临床开发中基于生物标志物的富集应降低后期试验的风险,最终扩大可供患者使用的创新IO药物组合。

相似文献

3
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
8
Thrombolysis for acute ischaemic stroke.急性缺血性脑卒中的溶栓治疗
Cochrane Database Syst Rev. 2003(3):CD000213. doi: 10.1002/14651858.CD000213.

本文引用的文献

3
Five latent factors underlie response to immunotherapy.五项潜在因素可预测免疫治疗应答。
Nat Genet. 2024 Oct;56(10):2112-2120. doi: 10.1038/s41588-024-01899-0. Epub 2024 Sep 12.
5
Tertiary lymphoid structures in anticancer immunity.肿瘤免疫中的三级淋巴结构
Nat Rev Cancer. 2024 Sep;24(9):629-646. doi: 10.1038/s41568-024-00728-0. Epub 2024 Aug 8.
6
Advances and prospects of biomarkers for immune checkpoint inhibitors.免疫检查点抑制剂生物标志物的研究进展与展望
Cell Rep Med. 2024 Jul 16;5(7):101621. doi: 10.1016/j.xcrm.2024.101621. Epub 2024 Jun 20.
8
Myeloid-derived suppressor cells in cancer and cancer therapy.髓源性抑制细胞在癌症和癌症治疗中的作用。
Nat Rev Clin Oncol. 2024 Feb;21(2):147-164. doi: 10.1038/s41571-023-00846-y. Epub 2024 Jan 8.
9
Balancing act: the complex role of NK cells in immune regulation.平衡之举:NK 细胞在免疫调节中的复杂作用。
Front Immunol. 2023 Nov 2;14:1275028. doi: 10.3389/fimmu.2023.1275028. eCollection 2023.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验