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Clinical Trial Summary

This is a multicenter, interventional, non-randomized study among patients with a relapsed or refractory Wilms tumor. The study will aim to assess efficacy of metronomic chemotherapy, in terms of disease control after two cycles of metronomic chemotherapy.


Clinical Trial Description

The main aim of this study is to assess efficacy of metronomic chemotherapy, in terms of disease control after two cycles of metronomic chemotherapy . Other objectives of the study include: - To evaluate disease control obtained with metronomic chemotherapy, in terms of progression-free survival (PFS) and overall survival (OS). - Evaluating early response after one cycle of treatment of metronomic treatment; - Evaluating best tumor response over the whole metronomic treatment duration; - Evaluating safety of the proposed metronomic chemotherapy; - Evaluating the feasibility of the proposed metronomic chemotherapy. - To evaluate quality of life using Kindl® Quality of Life questionnaire at baseline (before start of treatment), and approximately at weeks 7 and 13 of treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05384821
Study type Interventional
Source Centre Oscar Lambret
Contact Emilie Heyman - Decoupigny
Phone +33 (0)3 20 29 59 18
Email promotion@o-lambret.fr
Status Recruiting
Phase Phase 1/Phase 2
Start date September 14, 2022
Completion date October 2028

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