Department of Medical Oncology, Centre Antoine Lacassagne.
Université Côte d'Azur, Nice, France.
Curr Opin Oncol. 2019 May;31(3):146-151. doi: 10.1097/CCO.0000000000000522.
Checkpoint inhibitors (CPI) are revolutionizing the treatment of advanced cancers including recurrent and or metastatic squamous cell carcinoma of the head and neck (RM-SCCHN).
In this review, we will summarize the results of prospective trials evaluating CPI and particularly antiprogrammed death 1 (PD-1)/antiprogrammed death-ligand 1 (PD-L1) in RM-SCCHN.
Nivolumab and Pembrolizumab, two anti-PD-1 CPI, were associated with longer overall survival than standard chemotherapy in pretreated RM-SCCHN in two randomized phase 3 trials (respectively CHECKMATE-141 and KEYNOTE-040). Both are now approved in this setting. In the KEYNOTE-048 trial, the pembrolizumab was also associated with a longer survival when compared with the EXTREME regimen in first-line RM-SCCHN patients whose tumors overexpressed PD-L1 (combined positive score ≥20%). This trial also showed a superiority of platinum-based chemotherapy and pembrolizumab vs. EXTREME regimen in unselected first-line RM-SCCHN. Pembrolizumab will probably be the next standard of care for first-line RM-SCCHN with high expression of PD-L1. Further evaluation of CPI combined with other antitumoral agents is ongoing in advanced and locally advanced SCCHN.
检查点抑制剂(CPI)正在彻底改变包括复发性和/或转移性头颈部鳞状细胞癌(RM-SCCHN)在内的晚期癌症的治疗方法。
在这篇综述中,我们将总结评估 CPI,特别是抗程序性死亡受体 1(PD-1)/抗程序性死亡配体 1(PD-L1)在 RM-SCCHN 中的前瞻性试验结果。
在两项随机 3 期试验(分别为 CHECKMATE-141 和 KEYNOTE-040)中,两种抗 PD-1 CPI 药物纳武单抗和帕博利珠单抗与标准化疗相比,在预处理的 RM-SCCHN 中总生存期更长。这两种药物目前均在此适应证中获得批准。在 KEYNOTE-048 试验中,与 EXTREME 方案相比,在 PD-L1 过表达(综合阳性评分≥20%)的一线 RM-SCCHN 患者中,pembrolizumab 也与更长的生存时间相关。该试验还显示,在未选择的一线 RM-SCCHN 中,含铂化疗和 pembrolizumab 优于 EXTREME 方案。对于高表达 PD-L1 的一线 RM-SCCHN,pembrolizumab 可能成为下一个标准治疗方案。CPI 联合其他抗肿瘤药物在晚期和局部晚期 SCCHN 中的进一步评估正在进行中。