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Spots Global Cancer Trial Database for Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Ovarian Cancer (CHIPPI)

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Trial Identification

Brief Title: Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Ovarian Cancer (CHIPPI)

Official Title: Phase III Randomized Clinical Trial Evaluating Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Ovarian Cancer Considering Two Different Settings: Primary Debulking Surgery (PDS) and Interval Debulking Surgery (IDS)

Study ID: NCT03842982

Interventions

HIPEC

Study Description

Brief Summary: This is a phase III, multicenter, interventional and randomized study which evaluates the use of Hyperthermic Intraperitoneal Chemotherapy (HIPEC) coupled with either Primary Debulking Surgery (PDS) or Interval Debulking Surgery (IDS), in patients with ovarian cancer. This study aims to assess the efficacy, in terms of disease-free survival (DFS), the use of HIPEC combined with standard care (PDS or IDS) or standard care alone.

Detailed Description: 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

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Cliniques universitaires St-Luc, Institut Roi Albert II, Bruxelles, , Belgium

Institut de Cancérologie de l'Ouest, Angers, , France

Institut Bergonié, Bordeaux, , France

Centre François Baclesse, Caen, , France

Centre Jean Perrin, Clermont-Ferrand, , France

Centre Oscar Lambret, Lille, , France

Hôpital Jeanne de Flandre, Lille, , France

Institut Paoli Calmettes, Marseille, , France

ICM-Val d'Aurelle, Montpellier, , France

Hôpital Européen Georges Pompidou, Paris, , France

Centre Hospitalier Lyon Sud, Pierre-Bénite, , France

Clinique Mathilde, Rouen, , France

Centre Henri Becquerel, Rouen, , France

Institut de Cancérologie de l'Ouest, Saint-Herblain, , France

Hôpital de Hautepierre, Strasbourg, , France

Institut de Cancérologie de Lorraine, Vandœuvre-lès-Nancy, , France

Institut Gustave Roussy, Villejuif, , France

Contact Details

Name: Fabrice NARDUCCI, MD

Affiliation: Centre Oscar Lambret, Lille, France

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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