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Clinical Trial Summary

The purpose of this study is to determine if pharmacokinetics of docetaxel is modified by the body composition (assessed by the BMI but also by CT-scan) in patients treated by docetaxel as adjuvant treatment of a localized breast cancer


Clinical Trial Description

Half of the patients treated for a localized breast cancer are obese or overweighted. Recently published post-hoc analyses of a large randomised trial (BIG-2-98) revealed that BMI could impact the benefit of a docetaxel based chemotherapy, but not of an anthracyclin based chemotherapy. One of the hypothesis is that the distribution volume of hydrophobic drugs, such as docetaxel, may be influenced by the BMI, and more precisely by the amount of total fat. In that context, we aim to assess the docetaxel pharmacokinetics during its first exposure for localized breast cancer, and compare these results according to 3 groups of patients (lean, overweight and obese). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05858398
Study type Interventional
Source Centre Henri Becquerel
Contact Florian Clatot, Prof
Phone +33232082231
Email florian.clatot@chb.unicancer.fr
Status Not yet recruiting
Phase N/A
Start date May 30, 2023
Completion date May 2, 2026

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