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Induction chemotherapy in head and neck cancer: Results of a phase III trial

✍ Scribed by Dr. Jean-Jacques Mazeron; Michel Martin; Bernard Brun; Laval Grimard; Gilles Lelièvre; Laurence Vergnes; Elias Haddad; Frank Feuilhade; Pascal Piedbois; W. Strunski; Roger Peynègre; Bernard Pierquin; Jean-Paul Le Bourgeois


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
661 KB
Volume
14
Category
Article
ISSN
1043-3074

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✦ Synopsis


stage 11-Ill-IV squamous cell carcinoma of the oropharynx or oral cavity were randomized to induction chemotherapy, consisting of bleomycin (10 mg/m*/day in continuous infusion from day 1 to day 5), methotrexate (120 mg/m2 on day 2) followed by folink acid, 5-fluorouracil (5 FU) (600 mg/m2 on day 2), and cisplatin (120 mg/m2 on day 4) every 4 weeks for a total of three cycles followed by definitive locoregional treatment versus locoregional treatment alone. The modalities of definitive treatment (radiotherapy * surgery) were chosen prior to randomization. A total of 11 6 patients were evaluable. Of 55 patients in the chemotherapy arm, four (7%) had a complete response (CR) and 23 (42%) a partial response (PR) following the induction regimen. At the completion of locoregional treatment, 76% (42 of 55) of patients in the experimental group were in CR compared to 89% (54 of 61) in the control group. There was no difference in survival, cause-specific survival, and pattern of relapse between both groups. The median survival was 22 months in the chemotherapy group and 29 months in the control group. Responders to chemotherapy did not fare better than nonresponders. Chemotherapy-related toxicities were few and most of them related to cisplatin which was reduced to 100 mg/m2 for 35 patients. There were no treatment-related deaths From the


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