Division of Hematology/Oncology, Department of Medicine, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Cancer. 2023 May 1;129(9):1319-1350. doi: 10.1002/cncr.34683. Epub 2023 Feb 27.
The availability of agents targeting the programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) immune checkpoint has transformed treatment of advanced and/or metastatic non-small cell lung cancer (NSCLC). However, a substantial proportion of patients treated with these agents do not respond or experience only a brief period of clinical benefit. Even among those whose disease responds, many subsequently experience disease progression. Consequently, novel approaches are needed that enhance antitumor immunity and counter resistance to PD-(L)1 inhibitors, thereby improving and/or prolonging responses and patient outcomes, in both PD-(L)1 inhibitor-sensitive and inhibitor-resistant NSCLC. Mechanisms contributing to sensitivity and/or resistance to PD-(L)1 inhibitors in NSCLC include upregulation of other immune checkpoints and/or the presence of an immunosuppressive tumor microenvironment, which represent potential targets for new therapies. This review explores novel therapeutic regimens under investigation for enhancing responses to PD-(L)1 inhibitors and countering resistance, and summarizes the latest clinical evidence in NSCLC.
靶向程序性死亡蛋白 1(PD-1)/程序性死亡配体 1(PD-L1)免疫检查点的药物的出现改变了晚期和/或转移性非小细胞肺癌(NSCLC)的治疗方法。然而,相当一部分接受这些药物治疗的患者没有反应或仅经历短暂的临床获益。即使在那些疾病有反应的患者中,许多患者随后也会出现疾病进展。因此,需要新的方法来增强抗肿瘤免疫并对抗 PD-(L)1 抑制剂的耐药性,从而改善和/或延长对 PD-(L)1 抑制剂敏感和耐药性的 NSCLC 的反应和患者结局。导致 NSCLC 对 PD-(L)1 抑制剂的敏感性和耐药性的机制包括其他免疫检查点的上调和/或存在免疫抑制性肿瘤微环境,这代表了新疗法的潜在靶点。本综述探讨了正在研究用于增强对 PD-(L)1 抑制剂的反应和对抗耐药性的新治疗方案,并总结了 NSCLC 的最新临床证据。