Shanghai Institute of Immunology, Department of Immunology and Microbiology, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
School of Life Science and Technology, Changchun University of Science and Technology, Changchun, People's Republic of China.
Oncologist. 2019 Feb;24(Suppl 1):S31-S41. doi: 10.1634/theoncologist.2019-IO-S1-s05.
The use of immune checkpoint inhibitors (ICIs) has become one of the most promising approaches in the field of cancer therapy. Unlike the current therapies that target tumor cells, such as chemotherapy, radiotherapy, or targeted therapy, ICIs directly restore the exhausted host antitumor immune responses mediated by the tumors. Among multiple immune modulators identified, the programmed cell death protein 1 (PD-1)/programmed cell death protein ligand 1 (PD-L1) axis leading to the exhaustion of T-cell immunity in chronic infections and tumors has been widely investigated. Therefore, blocking antibodies targeting PD-1 or PD-L1 have been developed and approved for the treatment of various advanced cancers, including non-small-cell lung cancer (NSCLC), making them the most successful ICIs. Compared with chemotherapy or radiotherapy, PD-1/PD-L1 blockade therapy significantly improves the durable response rate and prolongs long-term survival with limited adverse effects in both monotherapy and combination therapy for advanced NSCLC. However, extensive challenges exist for further clinical applications, such as a small fraction of benefit population, primary and acquired resistance, the lack of predictive and prognostic biomarkers, and treatment-related adverse effects. In this article, we summarize the latest clinical applications of PD-1/PD-L1 blockade therapy in advanced NSCLC worldwide, as well as in China, and discuss the bottlenecks related to the use of this therapy in clinical practice. An exploration of the underlying mechanism of PD-1/PD-L1 blockade therapy and biomarker identification will maximize the application of ICIs in advanced NSCLC and facilitate bedside-to-bench studies in cancer immunotherapy as well. IMPLICATIONS FOR PRACTICE: Immune checkpoint inhibitors (ICIs) targeting programmed cell death protein 1 (PD-1) and programmed cell death protein ligand 1 (PD-L1) display apparent benefits for the treatment of advanced non-small-cell lung cancer (NSCLC). However, the clinical applications of these therapies are challenged by the limited benefit population with additional high economic burden and adverse events. This review discusses the bottlenecks of ICI therapy in clinical practice and provides appropriate guidance in the development of predictive biomarkers, the establishment of the criteria for combining PD-1/PD-L1 blockade therapy with the existing therapies, and the management of adverse events observed both in monotherapy and combination therapy, which will help maximize the applications of ICIs in advanced NSCLC.
免疫检查点抑制剂(ICIs)的应用已成为癌症治疗领域最有前途的方法之一。与目前针对肿瘤细胞的治疗方法(如化疗、放疗或靶向治疗)不同,ICIs 直接恢复肿瘤介导的耗尽的宿主抗肿瘤免疫反应。在已鉴定的多种免疫调节剂中,程序性细胞死亡蛋白 1(PD-1)/程序性细胞死亡蛋白配体 1(PD-L1)轴导致慢性感染和肿瘤中 T 细胞免疫衰竭已得到广泛研究。因此,已开发并批准了针对各种晚期癌症(包括非小细胞肺癌(NSCLC))的靶向 PD-1 或 PD-L1 的阻断抗体,使其成为最成功的 ICIs。与化疗或放疗相比,PD-1/PD-L1 阻断治疗在晚期 NSCLC 的单药和联合治疗中均具有显著提高持久缓解率和延长长期生存的作用,且不良反应有限。然而,进一步的临床应用仍面临广泛挑战,例如受益人群比例较小、原发和获得性耐药、缺乏预测和预后生物标志物以及与治疗相关的不良反应。本文总结了 PD-1/PD-L1 阻断治疗在全球和中国晚期 NSCLC 中的最新临床应用,并讨论了该治疗方法在临床实践中应用的相关瓶颈。探索 PD-1/PD-L1 阻断治疗的潜在机制和生物标志物鉴定将最大限度地提高 ICIs 在晚期 NSCLC 中的应用,并促进癌症免疫治疗的床旁到基础研究。
针对程序性细胞死亡蛋白 1(PD-1)和程序性细胞死亡蛋白配体 1(PD-L1)的免疫检查点抑制剂(ICIs)在治疗晚期非小细胞肺癌(NSCLC)方面显示出明显的益处。然而,这些治疗方法的临床应用受到受益人群有限、额外的高经济负担和不良反应的挑战。本文讨论了 ICI 治疗在临床实践中的瓶颈,并为预测生物标志物的开发、建立 PD-1/PD-L1 阻断治疗与现有治疗方法相结合的标准以及管理单药和联合治疗中观察到的不良反应提供了适当的指导,这将有助于最大限度地提高 ICIs 在晚期 NSCLC 中的应用。