It is a an open label, multicentric, phase II study assessing the efficacy of everolimus (given per os) as a first line treatment in kidney cancer of bad prognosis. 92 patients will be included (anticipated). The treatment by everolimus will continue until progression, significant toxicity or withdraw of consent
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
61
10 mg (1 tablet of 10 mg)
Gustave Roussy
Villejuif, Val de Marne, France
Overall Survival (OS)
Time frame: From inclusion to progression, significant toxicity or death wichever come first up to 56 months
Response rate
Response rate based on RECIST 1.1 criteria
Time frame: From inclusion to progression, significant toxicity or death whichever come first up to 56 months
Toxicity of Everolimus
Time frame: From inclusion to progression, significant toxicity or death whichever come first up to 56 months
Progression Free Survival (PFS)
Time frame: From inclusion to progression, significant toxicity or death whichever come first up to 56 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.