Mes données de santé
The information site for patients treated within the Unicancer network or included in Unicancer network clinical trials. 
Objectives

To describe progression-free survival of patients treated by subsequent chemotherapy following PARPi exposure in relapsing high-grade ovarian cancer defined as time to second progression (the time between first progression to second progression or death)

a. To describe overall survival of patients treated by subsequent chemotherapy following PARPi exposure in relapsing high-grade ovarian cancer b. To describe progression-free and overall survivals of patients treated by subsequent chemotherapy following PARPi exposure in relapsing high-grade ovarian cancer defined as time to second progression (the time between first progression to second progression or death) in the following subgroups: • BRCA1/2 mutated population • HRD population • BRCA1/2 negative, HRP negative population • BRCA ½ negative and HRD status unknown c. To describe the prognosis of patients following PARPi progression by evaluating Overall survival

Data controller

Institut de Cancérologie de l'Ouest

Categories of data used
Données d’identification (sans donnée nominative) / Données de santé
Origine de données utilisées
Soins
Institut de Cancérologie de l'Ouest (Nantes et Angers)
2005
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
Population subject to research or data processing

Patientes atteintes d'une tumeur de l'ovaire

Legal basis

 6.1.e) RGPD le traitement est nécessaire à l'exécution d'une mission d'intérêt public

Internal and external data recipients

Institut de cancérologie de l'Ouest

Research start date
01/03/2022
Data retention period

Conservation pendant 2 ans après la valorisation (publication/article, these, présentation orale, poster, autre) des résultats de la recherche. Puis archivage avec un accès restreint aux personnes intervenant dans la recherche, pendant une durée limitée de 3 ans (5ans au total post publication)

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