To evaluate the efficacy of the concomitant combination of radiotherapy and docetaxel with or without cisplatin in terms of objective response rates (WHO criteria).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
86
Sanofi-Aventis
Paris, France
Objective response rates
Time frame: evaluated 8 weeks after the end of radiotherapy
Duration of the responses and overall survival
Time frame: time until progression
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