Takeda M et al. – Patients in arm A will receive docetaxel at 60mg/m2 and those in arm B will receive docetaxel at 60mg/m2 plus bevacizumab at 15mg/kg, with each drug administered on day 1 every 21 days until progression or unacceptable toxicity. The primary endpoint of the study is progression–free survival, with secondary endpoints including response rate, overall survival, and safety, for patients treated in either arm.
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