Finding studies
Finding studies
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Lead
University of Turin, Italy
Primary Objective: To compare the activity of the 2 regimens The primary end point will be the clinical complete response rate of each treatment arm among all registered cases (intent to treat analysis). Secondary Objectives: To compare the 2 treatment arms with respect to: * Toxicity * Progression Free Survival * Overall survival Ancillary studies To evaluate before and after treatment a number of markers of hypoxia, neoangiogenesis, apoptosis, EGFR activating pathways.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted