Savolitinib plus cetuximab in recurrent/metastatic head and neck squamous cell carcinoma with EGFR and MET amplification after cetuximab-based therapy: A case report

The limited availability of targetable genomic alterations in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC) often results in suboptimal outcomes when utilizing targeted therapies. This case report describes a 57-year-old non-smoker male patient who was initially diagnosed with stage I (pT1cN0M0) tongue squamous cell carcinoma (AJCC 8th edition), characterized by EGFR overexpression. The combination therapy with TPEx regimen (Cetuximab, docetaxel, and cisplatin) led to a partial response. Over the following two years, the patient developed multiple metastatic lesions, including a lung lesion confirmed as metastatic squamous cell carcinoma harboring EGFR and MET co-amplification. Treatment with Savolitinib plus Cetuximab was associated with a reduction in metastatic lesions within two months, with a best response of partial response and a progression-free survival of 8.1 months. Unfortunately, the disease advanced, leading to liver metastasis and subsequent multi-organ failure. This case highlights that patients with MET amplification following progression on EGFR-targeted therapies may attain considerable clinical benefit from combination therapy with Savolitinib and Cetuximab, potentially overcoming MET-mediated resistance to EGFR inhibitors. These findings suggested that this combination may have clinical activity and supports further investigation in similar clinical scenarios.

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Publication Details

Journal
Medical Reports
Published
2026-11-01
DOI
https://doi.org/10.1016/j.hmedic.2026.100517
Primary Topic
Head and Neck Cancer Studies
Type
article
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article

Savolitinib plus cetuximab in recurrent/metastatic head and neck squamous cell carcinoma with EGFR and MET amplification after cetuximab-based therapy: A case report

Jiacheng Dai, Lin Zhang, Yaqian Han, Zheng Wu et al.
Medical Reports
Head and Neck Cancer Studies
article

Savolitinib plus cetuximab in recurrent/metastatic head and neck squamous cell carcinoma with EGFR and MET amplification after cetuximab-based therapy: A case report

Jiacheng Dai, Lin Zhang, Yaqian Han, Zheng Wu, Huai Liu, Yongchang Zhang, Hongzhi Ma
article en

Abstract

The limited availability of targetable genomic alterations in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC) often results in suboptimal outcomes when utilizing targeted therapies. This case report describes a 57-year-old non-smoker male patient who was initially diagnosed with stage I (pT1cN0M0) tongue squamous cell carcinoma (AJCC 8th edition), characterized by EGFR overexpression. The combination therapy with TPEx regimen (Cetuximab, docetaxel, and cisplatin) led to a partial response. Over the following two years, the patient developed multiple metastatic lesions, including a lung lesion confirmed as metastatic squamous cell carcinoma harboring EGFR and MET co-amplification. Treatment with Savolitinib plus Cetuximab was associated with a reduction in metastatic lesions within two months, with a best response of partial response and a progression-free survival of 8.1 months. Unfortunately, the disease advanced, leading to liver metastasis and subsequent multi-organ failure. This case highlights that patients with MET amplification following progression on EGFR-targeted therapies may attain considerable clinical benefit from combination therapy with Savolitinib and Cetuximab, potentially overcoming MET-mediated resistance to EGFR inhibitors. These findings suggested that this combination may have clinical activity and supports further investigation in similar clinical scenarios.

Medical Reports
Central South University (CN), Hunan Cancer Hospital (CN)
Openalex Percentile: Top 9%
Head and Neck Cancer Studies
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Savolitinib plus cetuximab in recurrent/metastatic head and neck squamous cell carcinoma with EGFR and MET amplification after cetuximab-based therapy: A case report — Jiacheng Dai, Lin Zhang, et al. · Medical Reports (2026) | TGRS Research Map | TGRS