From the Division of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Cancer J. 2020 Nov/Dec;26(6):507-516. doi: 10.1097/PPO.0000000000000483.
Immune checkpoint inhibitors (ICIs) have revolutionized the treatment paradigm for advanced non-small cell lung cancer (NSCLC). Although certain patients achieve significant, long-lasting responses from checkpoint blockade, the majority of patients with NSCLC do not and may be unnecessarily exposed to inadequate therapies and immune-related toxicities. Therefore, there is a critical need to identify biomarkers predictive of immunotherapy response. While tumor and immune cell expression of programmed death ligand-1 and, more recently, tumor mutational burden are used in clinical practice and may correlate with immunotherapy response in selected circumstances, neither consistently predicts an individual patient's likelihood of clinical benefit from ICI therapy. More recently, innovative approaches such as blood-based assays and combination biomarker strategies are under active investigation. This review will focus on the current role and challenges of programmed death ligand-1 and tumor mutational burden as predictive biomarkers for immunotherapy response in advanced NSCLC and explore promising novel biomarker strategies.
免疫检查点抑制剂 (ICIs) 彻底改变了晚期非小细胞肺癌 (NSCLC) 的治疗模式。尽管某些患者对检查点阻断有显著且持久的反应,但大多数 NSCLC 患者并未如此,并且可能不必要地接受了不充分的治疗和免疫相关毒性。因此,迫切需要识别预测免疫治疗反应的生物标志物。虽然肿瘤和免疫细胞程序性死亡配体-1 的表达,以及最近的肿瘤突变负担,在临床实践中得到了应用,并且在某些情况下可能与免疫治疗反应相关,但它们都不能一致地预测个体患者从 ICI 治疗中获益的可能性。最近,基于血液的检测和联合生物标志物策略等创新方法正在积极研究中。本文将重点讨论程序性死亡配体-1 和肿瘤突变负担作为晚期 NSCLC 免疫治疗反应预测生物标志物的当前作用和挑战,并探讨有前途的新型生物标志物策略。