A Pilot Clinical Trial of Cetuximab Combined With Tislelizumab as Neoadjuvant Therapy for Locally Advanced Oral Squamous Cell Carcinoma

BACKGROUND: Chemotherapy-free neoadjuvant strategies remain undefined for patients with locally advanced oral squamous cell carcinoma (OSCC) who are medically unsuitable for conventional cytotoxic chemotherapy. METHODS: In this prospective single-arm pilot trial, 15 patients received two cycles of neoadjuvant tislelizumab plus cetuximab before planned surgery. The primary endpoint was major pathological response (MPR). RESULTS: All patients completed neoadjuvant treatment and underwent radiographic assessment. The objective response rate was 73.3%. Twelve patients underwent surgery; five achieved MPR and two achieved pathological complete response. At a median follow-up of 23 months, the 2-year event-free survival and overall survival rates were 66.0% and 78.3%, respectively. No treatment-related deaths occurred. CONCLUSIONS: Neoadjuvant cetuximab plus tislelizumab showed feasible delivery, encouraging antitumor activity, and acceptable safety in patients with locally advanced OSCC who were medically unsuitable for conventional cytotoxic chemotherapy.

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Publication Details

Journal
Head & Neck
Published
2026-09-06
DOI
https://doi.org/10.1002/hed.70463
Primary Topic
Head and Neck Cancer Studies
Type
article
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article

A Pilot Clinical Trial of Cetuximab Combined With Tislelizumab as Neoadjuvant Therapy for Locally Advanced Oral Squamous Cell Carcinoma

Pu-Gen An, Wenjie Wu, Jian-Yun Zhang, Yan Chen et al.
Head & Neck
Head and Neck Cancer Studies
article

A Pilot Clinical Trial of Cetuximab Combined With Tislelizumab as Neoadjuvant Therapy for Locally Advanced Oral Squamous Cell Carcinoma

Pu-Gen An, Wenjie Wu, Jian-Yun Zhang, Yan Chen, Xiao Hu, Jie Yao, Jie Zhang
article en

Abstract

BACKGROUND: Chemotherapy-free neoadjuvant strategies remain undefined for patients with locally advanced oral squamous cell carcinoma (OSCC) who are medically unsuitable for conventional cytotoxic chemotherapy. METHODS: In this prospective single-arm pilot trial, 15 patients received two cycles of neoadjuvant tislelizumab plus cetuximab before planned surgery. The primary endpoint was major pathological response (MPR). RESULTS: All patients completed neoadjuvant treatment and underwent radiographic assessment. The objective response rate was 73.3%. Twelve patients underwent surgery; five achieved MPR and two achieved pathological complete response. At a median follow-up of 23 months, the 2-year event-free survival and overall survival rates were 66.0% and 78.3%, respectively. No treatment-related deaths occurred. CONCLUSIONS: Neoadjuvant cetuximab plus tislelizumab showed feasible delivery, encouraging antitumor activity, and acceptable safety in patients with locally advanced OSCC who were medically unsuitable for conventional cytotoxic chemotherapy.

Head & Neck
King University (US), Capital Medical University (CN), Peking University (CN), National Clinical Research Center for Digestive Diseases (CN), Peking University School and Hospital of Stomatology (CN), National Clinical Research (US)
Good health and well-being
Openalex Percentile: Top 8%
Head and Neck Cancer Studies
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