Short-course pembrolizumab and continuous afatinib therapy for recurrent or metastatic head and neck squamous cell

Hsiang-Fong Kao1, Huai-Cheng Huang2, Bin-Chi Liao1

  • 1Department of Medical Oncology, National Taiwan University Cancer Center, No.57, Ln. 155, Sec. 3, Keelung Rd, Da'an Dist, Taipei, 106, Taiwan.

BMC Cancer
|November 28, 2022
PubMed
Abstract

Insights

This study found that a short course of anti-PD-1 therapy combined with an EGFR inhibitor (afatinib) showed promising efficacy and acceptable toxicity in recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients.

Area of Science:

  • Oncology
  • Immunotherapy
  • Head and Neck Cancer Research

Background:

  • The optimal duration of anti-PD-1 therapy in combination regimens is not well-established.
  • Epidermal growth factor receptor (EGFR) pathway inhibitors enhance T-cell mediated tumor killing.
  • Recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) has limited treatment options.

Purpose of the Study:

  • To evaluate the efficacy and safety of a short course of anti-PD-1 therapy combined with continuous EGFR inhibition (afatinib).
  • To assess survival outcomes in patients with R/M HNSCC treated with this combination regimen.

Main Methods:

  • Retrospective analysis of a real-world cohort of 51 R/M HNSCC patients treated with pembrolizumab and afatinib.
  • Review of patient characteristics, treatment details, efficacy, and toxicity data.
  • Survival analysis including progression-free survival (PFS) and overall survival (OS).

Main Results:

  • The objective response rate was 54.9% with a median PFS of 5.9 months and median OS of 10.5 months.
  • Common toxicities included diarrhea (62.7%), skin rash (43.1%), and mucositis (31.4%).
  • Long-term survival rates at 12, 24, 36, and 48 months were 47.0%, 22.5%, 17.7%, and 12.6%, respectively.

Conclusions:

  • Short course pembrolizumab with afatinib demonstrates acceptable efficacy and manageable toxicity in R/M HNSCC.
  • The observed durable responses and survival rates are comparable to those in prospective trials.
  • Further prospective investigation of short-course anti-PD-1 therapy, particularly with EGFR inhibitors, is warranted.