Global Regulatory and Scientific Policy, The Healthcare Business of Merck KGaA, Darmstadt, Germany.
Ecc-Oncology, Trier, Germany.
Clin Cancer Res. 2024 Nov 1;30(21):4822-4833. doi: 10.1158/1078-0432.CCR-24-0741.
Since 2011, the US FDA has approved 30 new drugs for use in advanced non-small cell lung cancer (NSCLC), mainly comprising tyrosine kinase inhibitors and immune checkpoint inhibitors. NSCLC with oncogene driver alterations is amenable to treatment with targeted drugs, usually small-molecule inhibitors. In these cases, the demonstration of high overall response rates, coupled with a lasting duration of response, has allowed for accelerated approval in the United States, based on single-cohort or multicohort trials. Confirmatory clinical evidence was subsequently provided through postmarketing trials. In NSCLC without such driver alterations, regulatory agencies in both the United States and the European Union set clinical evidence expectations that foster the conduct of studies primarily focused on determining survival or event-free survival, based on randomized controlled trial designs. This review analyzes the approval patterns of novel therapeutics for NSCLC with a focus on small-molecule inhibitors that target driver alterations, as well as biologics. The latter include mAbs inhibiting immune checkpoints like PD-(L)1 or cell surface receptors and antibody-drug conjugates, highly potent biologics linked to a cytotoxic compound. The differentiation of NSCLC into oncogene- and non-oncogene-addicted subtypes determines drug development strategies, the extent of the clinical development program, access to orphan drug development incentives, and regulatory approval strategies.
自 2011 年以来,美国食品和药物管理局(FDA)已批准 30 种新的药物用于治疗晚期非小细胞肺癌(NSCLC),主要包括酪氨酸激酶抑制剂和免疫检查点抑制剂。具有致癌基因驱动改变的 NSCLC 可以用靶向药物治疗,通常是小分子抑制剂。在这些情况下,由于单队列或多队列试验显示出高总缓解率,并且缓解持续时间较长,因此可以基于这些证据在美国加速批准。随后通过上市后试验提供了确认性临床证据。在没有这种驱动改变的 NSCLC 中,美国和欧盟的监管机构设定了临床证据期望,这些期望促进了主要侧重于确定生存或无事件生存的研究,这些研究基于随机对照试验设计。本综述分析了新型 NSCLC 治疗药物的批准模式,重点是针对驱动改变的小分子抑制剂以及生物制剂。后者包括 PD-(L)1 或细胞表面受体等免疫检查点的单克隆抗体抑制剂,以及与细胞毒性化合物连接的高效生物制剂抗体药物偶联物。将 NSCLC 分为致癌基因和非致癌基因依赖性亚型,决定了药物开发策略、临床开发计划的程度、获得孤儿药开发激励措施以及监管批准策略。