Finding studies
Finding studies
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Lead
Centre Oscar Lambret
The primary objective of this study is to assess the efficacy, in terms of disease-free survival (DFS), the use of HIPEC treatment combined with standard care (PDS or IDS) or standard care alone (PDS or IDS alone). Secondary objectives of the study include: * Evaluating the efficacy of HIPEC in terms of overall survival (OS) in combination with standard of care * Evaluating the morbidity associated with HIPEC. * Evaluating the trade-off between efficacy and morbidity using the Q-TWiST approach. * Evaluating the impact of HIPEC in terms of quality of life. Exploratory objectives (optional) include: * Evaluating the impact of HIPEC on the count of residual viable cells (evaluated by flow cytometry) in abdominal drainage fluids for patients recruited in Centre Oscar Lambret only. * Constituting a biobank (tumoral samples and blood samples) for future translational researches
Age
18–76
Sex
FEMALE
Healthy volunteers
Not accepted
