Lim Sun Min, Hong Min Hee, Kim Hye Ryun
Division of Hematology-Medical Oncology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Immune Netw. 2020 Jan 27;20(1):e10. doi: 10.4110/in.2020.20.e10. eCollection 2020 Feb.
Immune checkpoint inhibitors (ICIs) have shown remarkable benefit in the treatment of patients with non-small-cell lung cancer (NSCLC) and have emerged as an effective treatment option even in the first-line setting. ICIs can block inhibitory pathways that restrain the immune response against cancer, restoring and sustaining antitumor immunity. Currently, there are 4 PD-1/PD-L1 blocking agents available in clinics, and immunotherapy-based regimen alone or in combination with chemotherapy is now preferred option. Combination trials assessing combination of ICIs with chemotherapy, targeted therapy and other immunotherapy are ongoing. Controversies remain regarding the use of ICIs in targetable oncogene-addicted subpopulations, but their initial treatment recommendations remained unchanged, with specific tyrosine kinase inhibitors as the choice. For the majority of patients without targetable driver oncogenes, deciding between therapeutic options can be difficult due to lack of direct cross-comparison studies. There are continuous efforts to find predictive biomarkers to find those who respond better to ICIs. PD-L1 protein expressions by immunohistochemistry and tumor mutational burden have emerged as most well-validated biomarkers in multiple clinical trials. However, there still is a need to improve patient selection, and to establish the most effective concurrent or sequential combination therapies in different NSCLC clinical settings. In this review, we will introduce currently used ICIs in NSCLC and analyze most recent trials, and finally discuss how, when and for whom ICIs can be used to provide promising avenues for lung cancer treatment.
免疫检查点抑制剂(ICIs)在非小细胞肺癌(NSCLC)患者的治疗中已显示出显著疗效,甚至在一线治疗中也已成为一种有效的治疗选择。ICIs可以阻断抑制免疫反应对抗癌症的抑制途径,恢复并维持抗肿瘤免疫力。目前,临床上有4种PD-1/PD-L1阻断剂,基于免疫疗法的方案单独使用或与化疗联合使用现在是首选方案。评估ICIs与化疗、靶向治疗及其他免疫疗法联合使用的试验正在进行。关于ICIs在可靶向致癌基因成瘾亚群中的使用仍存在争议,但其初始治疗建议保持不变,仍选择特定的酪氨酸激酶抑制剂。对于大多数没有可靶向驱动致癌基因的患者,由于缺乏直接的交叉比较研究,在治疗方案之间做出决定可能很困难。人们一直在努力寻找预测生物标志物,以找出那些对ICIs反应更好的患者。通过免疫组织化学检测的PD-L1蛋白表达和肿瘤突变负荷已在多项临床试验中成为最得到充分验证的生物标志物。然而,仍有必要改进患者选择,并在不同的NSCLC临床环境中建立最有效的同步或序贯联合治疗方法。在这篇综述中,我们将介绍目前在NSCLC中使用的ICIs并分析最新试验,最后讨论ICIs如何、何时以及适用于哪些患者,以为肺癌治疗提供有前景的途径。