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Volume 64, Issue 4, Pages 983-994 (15 March 2006)


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French multicenter phase III randomized study testing concurrent twice-a-day radiotherapy and cisplatin/5-fluorouracil chemotherapy (BiRCF) in unresectable pharyngeal carcinoma: Results at 2 years (FNCLCC-GORTEC)

Presented at the 46th Annual Meeting of the American Society for Therapeutic Radiology and Oncology (ASTRO), Atlanta, GA, Oct 3–7, 2004.

René-Jean Bensadoun, M.D.Corresponding Author Informationemail address, Karen Bénézery, M.D., Olivier Dassonville, M.D., Nicolas Magné, M.D., Ph.D., Gilles Poissonnet, M.D., Alain Ramaïoli, M.D., Claire Lemanski, M.D.#, Sylvain Bourdin, M.D.⁎⁎, Jacques Tortochaux, M.D.††, Frédéric Peyrade, M.D., Pierre-Yves Marcy, M.D.§, Emmanuel Chamorey, Pharm.D., Jacques Vallicioni, M.D., Hang Seng, M.D.‡‡, Claude Alzieu, M.D.§§, Bernard Géry, M.D.∥∥, Pierre Chauvel, M.D., Maurice Schneider, M.D., Ph.D., José Santini, M.D., Ph.D., François Demard, M.D., Ph.D., Gilles Calais, M.D., Ph.D.¶¶

Received 6 May 2005; received in revised form 20 September 2005; accepted 27 September 2005. published online 23 December 2005.

Background: Unresectable carcinomas of the oropharynx and hypopharynx still have a poor long-term prognosis. Following a previous phase II study, this phase III multicenter trial was conducted between November 1997 and March 2002.

Methods: Nontreated, strictly unresectable cases were eligible. Twice-daily radiation: two fractions of 1.2 Gy/day, 5 days per week, with no split (D1→D46). Total tumor doses: 80.4 Gy/46 day (oropharynx), 75.6 Gy/44 day (hypopharynx). Chemotherapy (arm B): Cisplatin 100 mg/m2 (D1, D22, D43); 5FU, continuous infusion (D1→D5), 750 mg/m2/day cycle 1; 430 mg/m2/day cycles 2 and 3.

Results: A total of 163 evaluable patients. Grade 3–4 acute mucositis 82.6% arm B/69.5% arm A (NS); Grade 3–4 neutropenia 33.3% arm B/2.4% arm A (p < 0.05). Enteral nutrition through gastrostomy tube was more frequent in arm B before treatment and at 6 months (p < 0.01). At 24 months, overall survival (OS), disease-free survival (DFS), and specific survival (SS) were significantly better in arm B. OS: 37.8% arm B vs. 20.1% arm A (p = 0.038); DFS: 48.2% vs. 25.2% (p = 0.002); SS: 44.5% vs. 30.2% (p = 0.021). No significant difference between the two arms in the amount of side effects at 1 and 2 years.

Conclusion: For these unresectable cases, chemoradiation provides better outcome than radiation alone, even with an “aggressive” dose-intensity radiotherapy schedule.

 Department of Radiation Oncology, Centre Antoine Lacassagne, Nice, France

 Department of Head and Neck Surgery, Centre Antoine Lacassagne, Nice, France

 Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France

§ Department of Radiology, Centre Antoine Lacassagne, Nice, France

 Department of Statistics Unit, Centre Antoine Lacassagne, Nice, France

 Department of Otolaryngology, University Hospital, Nice, France

# Centre Val d’Aurelle—Paul Lamarque, Montpellier, France

⁎⁎ Centre René-Gauducheau, Nantes, France

†† Centre Jean-Perrin, Clermont-Ferrand, France

‡‡ Centre Henri-Becquerel, Rouen, France

§§ Institut Paoli-Calmettes, Marseille, France

∥∥ Centre François-Baclesse, Caen, France

¶¶ Hôpital Jean Bretonneau, Tours, France

Corresponding Author InformationReprint requests to: René-Jean Bensadoun, M.D., Centre Antoine Lacassagne, 33 avenue de Valombrose, 06189 Nice cedex 2, France. Tel: (+33) 4-9203-1270; Fax: (+33) 4-9203-1570

 The French “Fédération Nationale des Centres de Lutte Contre le Cancer” (FNCLCC) promoted the present study in relation with the “Groupe d’Oncologie Radiothérapie Tête et Cou” (GORTEC).

PII: S0360-3016(05)02712-4

doi:10.1016/j.ijrobp.2005.09.041


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