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免疫疗法在复发性和/或转移性头颈部鳞状细胞癌中的应用。

Immunotherapy in recurrent and or metastatic squamous cell carcinoma of the head and neck.

机构信息

Department of Medical Oncology, Centre Antoine Lacassagne.

Université Côte d'Azur, Nice, France.

出版信息

Curr Opin Oncol. 2019 May;31(3):146-151. doi: 10.1097/CCO.0000000000000522.

Abstract

PURPOSE OF REVIEW

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).

RECENT FINDINGS

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.

SUMMARY

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.

摘要

目的综述

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。

最新发现

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。

总结

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。

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