PD1/PD-L1 Axis Blockers in Head and Neck Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis of Efficacy and Safety Outcomes

PD1/PD-L1轴阻滞剂在头颈部鳞状细胞癌中的应用:疗效和安全性结果的系统评价和荟萃分析

阅读:1

Abstract

Cancers of the head and neck are common, and this review aimed to systematically analyze the safety and efficacy of anti-PD1/PD-L1 inhibitors (API) therapies in head and neck squamous cell carcinoma (HNSCC). This is a systematic review of randomized controlled trials (RCTs) showcasing the safety and efficacy of APIs in HNSCC. An online literature search of PubMed, Cochrane database, and ClinicalTrials.gov was conducted till May 31, 2024, to identify RCTs involving anti-PD1/PD-L1 therapies in oral cancer. The data were analyzed using Review Manager (RevMan) (Cochrane, London, United Kingdom), and the risk of bias was assessed for methodological quality. This study included nine RCTs with 3933 study participants. API treatment showed a significant improvement in overall survival (OS) compared to standard therapy in HNSCC (hazard ratio (HR) =0.85 (0.76,0.95), I(2)=26%, P=0.004). Even participants with PD-L1≥1%, treated with APIs, manifested substantial advancement of OS. Duration of response (DOR) was notably improved with API (HR= 0.31 (0.20, 0.50), I(2)=0%, P <0.00001) compared to standard therapy. Safety outcomes revealed comparatively reduced incidence of treatment-related adverse events and Grade 3/4 adverse effects when treated with APIs compared to standard therapy. In the era of emerging immunotherapy, APIs may be considered an alternative therapy in HNSCC, which could improve the OS, OS in patients with >1% PD-L1 expression, and DOR, as well as with a better safety profile as compared to chemotherapy and combination ICI. APIs pave the way for novel therapeutic strategies incorporating immune checkpoint inhibitors in HNSCC management.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。