Patients treated on the first line of Sunitinib-targeted therapy for metastatic kidney cancer. Collection of additional blood tubes during routine blood tests for patient follow-up, to evaluate the plasma concentration of Sunitinib and its active metabolite desethyl-Sunitinib (DES)
Study Type
OBSERVATIONAL
Enrollment
6
blood sample performed on C1D1, C1D14, C2D1, C3D1 and C6D1
CHU de ROUEN
Rouen, France
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
Time frame: At the end of Cycle 1 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
Time frame: At the end of Cycle 2 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
Time frame: At the end of Cycle 3 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
Time frame: At the end of Cycle 4 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
Time frame: At the end of Cycle 5 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biologicalas according to the plasma concentration of Sunitinib
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Time frame: At the end of Cycle 6 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 1 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 2 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 3 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 4 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 5 (each cycle is 28 days)
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
hazard ratio of a severe toxicity, grade 3-4 clinical and / or biological according to the plasma concentration of desethyl-Sunitinib
Time frame: At the end of Cycle 6 (each cycle is 28 days)
plasma desethyl-Sunitinib (DES) concentration
influence of plasma DES concentration on patients survival
Time frame: Cycle1 Day14 (each cycle is 28 days)
plasma Sunitinib concentration
influence of plasma Sunitinib concentration on patients survival
Time frame: Cycle1 Day14 (each cycle is 28 days)
plasma Sunitinib concentration
influence of plasma Sunitinib concentration on patients survivall
Time frame: Cycle1 Day28 (each cycle is 28 days)
plasma DES concentration
influence of plasma Sunitinib concentration on patients survival
Time frame: Cycle1 Day28 (each cycle is 28 days)
plasma Sunitinib concentration
influence of plasma Sunitinib concentration on patients survival
Time frame: Cycle2 Day28(each cycle is 28 days)
plasma DES concentration
influence of plasma DES concentration on patients survival
Time frame: Cycle2 Day28 (each cycle is 28 days)
plasma Sunitinib concentration
influence of plasma Sunitinib concentration on patients survival
Time frame: Cycle3 Day28 (each cycle is 28 days)
plasma DES concentration
Evaluate the influence of plasma DES concentration on patients survival
Time frame: Cycle3 Day28 (each cycle is 28 days)
plasma Sunitinib concentration
influence of plasma Sunitinib concentration on patients survival
Time frame: Cycle6 Day28 (each cycle is 28 days)
plasma DES concentration
influence of plasma DES concentration on patients survival
Time frame: Cycle6 Day28 (each cycle is 28 days)