4.7 Article

Afatinib and Pembrolizumab for Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (ALPHA Study): A Phase II Study with Biomarker Analysis

期刊

CLINICAL CANCER RESEARCH
卷 28, 期 8, 页码 1560-1571

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-21-3025

关键词

-

类别

资金

  1. Boehringer Ingelheim Taiwan for drug supply (afatinib)
  2. Merck Sharp & Dohme Corp (I.A.) LCC, Taiwan Branch for drug supply (pembrolizumab) - Ministry of Education, Taiwan [NTU-107L9014]
  3. Ministry of Science and Technology, Taiwan [MOST 107-3017-F-002-002]

向作者/读者索取更多资源

The study explores the potential of afatinib to enhance the efficacy of pembrolizumab in treating recurrent or metastatic HNSCC, promoting antigen presentation and immune activation to improve patient outcomes.
Purpose: EGFR pathway inhibition may promote anti- programmed cell death protein 1 (PD-1) responses in preclinical models, but how EGFR inhibition affects tumor antigen presentation during anti-PD-1 monotherapy in humans remain unknown. We hypothesized that afatinib, an irreversible EGFR tyrosine kinase inhibitor, would improve outcomes in patients treated with pembrolizumab for recurrent or metastatic head and neck squamous cell carcinoma (HNSCC) by promot-ing antigen presentation and immune activation in the tumor microenvironment. Patients and Methods: The ALPHA study (NCT03695510) was a single-arm, Phase II study with Simon's 2-stage design. Afatinib and pembrolizumab were administered to patients with platinum-refractory, recurrent, or metastatic HNSCC. The primary endpoint was the objective response rate (ORR). The study applied gene expression analysis using a NanoString PanCancer Immune Profiling Panel and next-generation sequencing using FoundationOne CDx. Results: From January 2019 to March 2020, the study enrolled 29 eligible patients. Common treatment-related adverse events were skin rash (75.9%), diarrhea (58.6%), and paronychia (44.8%). Twelve patients (41.4%) had an objective partial response to treatment. The median progression-free survival was 4.1 months, and the median overall survival was 8.9 months. In a paired tissue analysis, afatinib- pembrolizumab were found to upregulate genes involved in antigen presentation, immune activation, and natural killer cell-mediated cytotoxicity. Unaltered methylthioadenosine phosphorylase and EGFR amplification may predict the clinical response to the therapy. Conclusions: Afatinib may augment pembrolizumab therapy and improve the ORR in patients with HNSCC. Bioinformatics analysis suggested the enhancement of antigen presentation machinery in the tumor microenvironment.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据