Anti-epidermal growth factor receptor therapy in combination with chemoradiotherapy for the treatment of locally advanced anal canal carcinoma: Results of a phase I dose-escalation study with panitumumab (FFCD 0904)

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TitreAnti-epidermal growth factor receptor therapy in combination with chemoradiotherapy for the treatment of locally advanced anal canal carcinoma: Results of a phase I dose-escalation study with panitumumab (FFCD 0904)
Type de publicationJournal Article
Year of Publication2019
AuteursVendrely V, Lemanski C, Gnep K, Barbier E, Hajbi FEl, Lledo G, Dahan L, Terrebonne E, Manfredi S, Mirabel X, Mammar V, Cowen D, Lepage C, Aparicio T, Collaborators FFCDInvestigat
JournalRADIOTHERAPY AND ONCOLOGY
Volume140
Pagination84-89
Date PublishedNOV
Type of ArticleArticle
ISSN0167-8140
Mots-clésAnal cancer, chemoradiotherapy, Epidermal growth factor receptor, Immunotherapy, Panitumumab, Squamous cell carcinoma
Résumé

Background and purpose: Standard treatment of epidermoid anal cancer is 5-fluorouracil (5FU) and mitomycin C (MMC) based chemoradiotherapy (CRT). This phase I study aims to evaluate the addition of panitumumab (Pmab) to CRT and to determine the maximum tolerated dose (MTD) of Pmab and 5-FU in combination with CRT. Materials and methods: Immunocompetent patients with locally advanced tumour without metastases (Stage T2, T3 or T4, whatever N stage; Stage N1-N3 whatever T stage) followed two RT periods (45 Gy in 5 weeks and 20 Gy in 2 weeks, separated by a 2-week break) with concomitant CT sessions of 5FU/MMC at RT weeks 1, 5 and 8. Pmab was administered on RT weeks 1, 3, 5, 8 and 10 according to a predefined dose escalation schedule. Results: Ten patients were enroled. One was excluded due to unmet dose constraints respect. Three patients received dose level (DL) 0 (Pmab 3 mg/kg + 5FU 600 mg/m(2)/day) and six received DL-1 (Pmab 3 mg/kg + 5FU 400 mg/m(2)/day). Dose-limiting toxicities occurred in all patients at DL 0 and 2 at DL-1. Most common grade 3-4 toxicities observed at DL 0 were haematologic (100%), dermatitis (67%), and anaemia (67%). No death occurred. Four months after ending CRT, five and two patients had a local complete response and a partial response, respectively. One patient had a colostomy with abdomino-perineal amputation due to a tumour recurrence. Conclusions: The MTD is 5FU at 400 mg/m(2)/day, MMC at 10 mg/m(2) and Pmab at 3 mg/kg. The effect of the MTD on tumour response is evaluated in the phase 2 study. (C) 2019 Elsevier B.V. All rights reserved.

DOI10.1016/j.radonc.2019.05.018