The purpose of the study is to evaluate the ration of patients getting an lighten therapeutic strategy after 18F-fluoro-désoxyglucose positron emission tomography (PET-TDM) in grade I (cohort 1) or metastatic (cohort 2) seminoma
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
271
\- carboplatine: Dose (mg) = AUC x (GFR + 25) * GFR : glomérulaire filtration (ml/min) * AUC : area under curve (mg/ml x min)
100 mg/m2 D1 to D5
20 mg/m2 de D1 to D5
Gustave Roussy
Villejuif, Val de Marne, France
RECRUITINGRate of patients without pathological fixation
Rate of patients without pathological fixation at the time of the inclusion PET-TDM (cohort 1) or at the time of the PET-TDM following two cycles of chemotherapy (Etoposiede+Cisplatine) (cohort 2) and getting a lighten protocol
Time frame: Assessed at the time of inclusion or after 2 cycles of chemotherapy, up to 21 days
Rate of patients without pathological fixation
Rate of patients without pathological fixation at the time of the inclusion PET-TDM (cohort 1) or at the time of the PET-TDM following two cycles of chemotherapy (Etoposiede+Cisplatine) (cohort 2)
Time frame: Assessed at the time of inclusion or after 2 cycles of chemotherapy, up to 21 days
Progression Free Survival (PFS)
Time frame: Assessed up to 5 years
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