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Phase 1 trial of concurrent erlotinib, celecoxib, and reirradiation for recurrent head and neck cancer
Author(s) -
Kao Johnny,
Genden Eric M.,
Chen ChienTing,
Rivera Michael,
Tong Charles C. L.,
Misiukiewicz Kryztof,
Gupta Vishal,
Gurudutt Vivek,
Teng Marita,
Packer Stuart H.
Publication year - 2011
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.25786
Subject(s) - medicine , erlotinib , head and neck cancer , regimen , mucositis , celecoxib , erlotinib hydrochloride , oncology , cetuximab , cancer , egfr inhibitors , surgery , epidermal growth factor receptor , radiation therapy , colorectal cancer
BACKGROUND: Concurrent inhibition of epidermal growth factor receptor (EGFR) and cyclooxygenase‐2 (COX‐2) is an active and well tolerated regimen in recurrent head and neck cancer (HNC). In the current phase 1 trial, the authors sought to determine the maximum tolerated dose (MTD) and efficacy of concurrent erlotinib and celecoxib as a radiosensitizing regimen. METHODS: Fourteen patients with previously irradiated HNC with no distant metastases who required reirradiation were eligible. Treatment consisted of daily erlotinib 150 mg and twice daily celecoxib (escalated from 200 mg to 600 mg using a 3 + 3 design with an expanded cohort at the MTD) starting on Day 1 and was continued during radiation. Daily radiation was started on Day 15, and maintenance erlotinib was recommended. RESULTS: The recommended phase 2 dose of celecoxib was 400 mg. Three dose‐limiting toxicities included late in‐field orocutaneous fistula (Dose Level 2), osteonecrosis (Dose Level 3), and trismus (Dose Level 3). Acute grade ≥3 toxicities were uncommon and included mucositis (21%) and dermatitis (14%). At a median follow‐up of 11 months, the 1‐year locoregional control, progression‐free survival, and overall survival rates were 60%, 37%, and 55%, respectively. CONCLUSIONS: Concurrent erlotinib, celecoxib, and reirradiation was a feasible and clinically active regimen in a population of patients with recurrent HNC who had a poor prognosis. Cancer 2011. © 2011 American Cancer Society.