Emens Leisha A, Moussion Christine, Hwu Patrick, Gulley James L, Ohashi Pamela S, Bifulco Carlo B, Feltquate David
Kaiser Permanente, South Sacramento, California, USA
Genentech, South San Francisco, California, USA.
J Immunother Cancer. 2025 Jun 22;13(6):e010739. doi: 10.1136/jitc-2024-010739.
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.
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。