Gridelli Cesare, Ardizzoni Andrea, Barberis Massimo, Cappuzzo Federico, Casaluce Francesca, Danesi Romano, Troncone Giancarlo, De Marinis Filippo
Division of Medical Oncology, 'S. G. Moscati' Hospital, Avellino, Italy.
Department of Medical Oncology, AOU di Bologna, Policlinico S. Orsola Malpighi, Bologna, Italy.
Transl Lung Cancer Res. 2017 Jun;6(3):373-386. doi: 10.21037/tlcr.2017.05.09.
Unleashing the potential of immune system to fight cancer has become one of the main promising treatment modalities for advanced non-small cell lung cancer (NSCLC). The knowledge of numerous factors that come into play in the cancer-immunity cycle provide a wide range of potential therapeutic targets, including monoclonal antibodies that inhibits the programmed death-1 (PD-1) checkpoint pathway. Over the last two years, nivolumab, pembrolizumab and atezolizumab received approval for treatment of pretreated advanced NSCLC, and more recently, immunotherapy with pembrolizumab is the new standard of care as first-line in patients with high levels of programmed death-ligand 1 (PD-L1) expression. Selection of patients is mandatory and PD-L1 is the only biomarker currently available in clinical practice. However, PD-L1 staining is an imperfect marker, whose negativity does not exclude a response to immunotherapy, as well as the roughly half of patients are "not-responders" despite high tumor PD-L1 levels. The right cut-off, the differences among various immune checkpoint inhibitors and among various antibody clones, and a not trivial activity reported even in PD-L1 negative tumors are questions still open. New biomarkers beyond to PD-L1 assays as well as new strategies, including combination of immune checkpoint inhibitors are under investigation.
释放免疫系统对抗癌症的潜力已成为晚期非小细胞肺癌(NSCLC)主要的有前景的治疗方式之一。对癌症免疫循环中众多起作用的因素的了解提供了广泛的潜在治疗靶点,包括抑制程序性死亡-1(PD-1)检查点通路的单克隆抗体。在过去两年中,纳武单抗、派姆单抗和阿特珠单抗获批用于治疗经治的晚期NSCLC,最近,派姆单抗免疫疗法成为程序性死亡配体1(PD-L1)高表达患者一线治疗的新标准。患者选择至关重要,PD-L1是目前临床实践中唯一可用的生物标志物。然而,PD-L1染色是一种不完善的标志物,其阴性并不排除对免疫疗法有反应,而且尽管肿瘤PD-L1水平高,仍有大约一半的患者“无反应”。合适的临界值、各种免疫检查点抑制剂之间以及各种抗体克隆之间的差异,甚至在PD-L1阴性肿瘤中报道的显著活性,这些问题仍然悬而未决。除了PD-L1检测之外的新生物标志物以及包括免疫检查点抑制剂联合在内的新策略正在研究中。