Prospective Pilot Study of Second Primary Tumor Prevention With Erlotinib and Celecoxib in Early-Stage Squamous Cell Carcinoma of the Head and Neck: Long-Term Follow-Up.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 40296503.
- Also identified by DOI 10.1002/hed.28178 and PMC identifier 12339201.
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Abstract
Patients with early-stage head and neck squamous cell carcinoma (HNSCC) have an increased risk for secondary primary tumors (SPT) after definitive treatment. The aim of this pilot trial was to investigate the safety and efficacy of erlotinib and celecoxib in preventing SPTs. Ten patients with stage I/II HNSCC who completed definitive treatment received erlotinib with celecoxib for 6 months. Primary objectives were safety assessment and SPT-free survival after completion of erlotinib and celecoxib. Secondary objectives included assessing overall survival (OS) and progression-free survival (PFS). With a median follow-up of 9 (1.7-15.3) years, the median time to SPT-free survival was not reached. The estimated SPT-free survival was 78.8% at 15 years. Two patients had local recurrence, but none of our subjects developed mucosal squamous cell carcinoma at any site. All three doses of erlotinib and the fixed dose of celecoxib were well tolerated with excellent SPT-free survival with long-term follow-up. Clinicaltrials.gov identifier: NCT00400374.
Medical subject headings
- Antineoplastic Combined Chemotherapy Protocols
- Celecoxib
- Erlotinib Hydrochloride
- Neoplasms, Second Primary
- Squamous Cell Carcinoma of Head and Neck