Abstract

Recent studies have suggested the benefit of salvage chemotherapy (SCT) after immune checkpoint inhibitor (ICI) treatment for recurrent and metastatic head and neck squamous cell carcinoma (R/M HNSCC). We retrospectively examined the outcome of SCT and the usefulness of the serum C-reactive protein level (CRP) and neutrophil-to-lymphocyte ratio (NLR) as prognostic biomarkers. Thirty-nine patients with R/M HNSCC were enrolled in this study. Twenty-five patients (64.1%) received combination chemotherapy of weekly paclitaxel and cetuximab (PC) as SCT, and 14 patients (35.9%) received tegafur-gimestat-otastat potassium (S1), an oral fluoropyrimidine. In all patients, the response rate, disease control rate, median progression-free survival (PFS), and median overall survival (OS) were 45.2%, 85.7%, 6.5 months, and 13.5 months, respectively. No chemotherapy-related deaths were observed. These PC groups had low CRP (<1.2 mg/dL) or low NLR (<7.0) values at the time of SCT induction, which was significantly associated with an improved OS (p = 0.0440, p = 0.0354). A multivariate analysis also showed that a lower CRP value was significantly associated with a better OS (p = 0.0078). We clarified the usefulness of the PC and S1 regimens as SCT. In addition, SCT with the PC regimen showed a better prognosis with a lower CRP or NLR at induction than a higher CRP or NLR. This is the first report on biomarkers of SCT in R/M HNSCC.

Highlights

  • A paradigm shift in the treatment of recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) has occurred

  • From 1 April 2017 to 30 November 2019, 136 patients with R/M HNSCC were treated with nivolumab at Kyushu University Hospital, National Kyushu Cancer Center, and Kitakyushu Municipal

  • 39 patients were included in this retrospective study, including the 10 patients we have previously reported as a case series [11]

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Summary

Introduction

A paradigm shift in the treatment of recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) has occurred. For patients with progressive disease status after ICI treatment, another therapy sometimes could be administered to extend their life. Several studies have reported that salvage chemotherapy (SCT) administered after immunotherapy would be effective for patients with metastatic non-small-cell lung cancer (NSCLC), metastatic melanoma, B cell lymphoma, advanced gastric cancer, and metastatic urothelial carcinoma [3,4,5,6,7,8,9]. SCT has been reported to be an effective treatment for HNSCC in R/M as well as other carcinomas and is attracting attention as a sequential treatment [10,11]. Combination chemotherapy of weekly paclitaxel and cetuximab (PC) or oral tegafur-gimestat-otastat potassium (S1) is administered as SCT after ICI treatment in our institution and associated facilities. The long-term efficacy and prognosis vary greatly among patients

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