Survivorship after cancer and its late effects (SCALA)
Objectif(s) de la recherche et intérêt pour la santé publique
Finalité de l'étude
Objectifs poursuivis
Domaines médicaux investigués
Bénéfices attendus
The population of cancer survivors is rapidly growing owing to improvements in early detection and treatment of cancer. Quality of life, which encompasses physical, psychological and social well-being, is often altered in cancer survivors and remains understudied. The SCALA study aims to identify the major late and long-term consequences of cancer and its treatment amongst cancer survivors, their determinants and their impact on quality of life, overall and by cancer type. The study will be embedded in two existing and prospective large French cohorts (Constances and Gazel) with existing quality of life, social, lifestyle and health data collected at baseline and annually. These cohorts are linked to the SNDS, which has information on cancer diagnosis and treatment. Furthermore, extensive quality of life information will be newly collected in cancer survivors participating in these cohorts using a validated questionnaire. Findings from the SCALA study will provide immediate insights into the late and long-term effects of cancer and its treatment experienced by cancer survivors and their impact on quality of life. The study will also generate evidence to inform tertiary prevention of cancer through lifestyle modification and will help identify cancer survivors at higher risk of developing late and long-term effects who would thus need reinforced surveillance and advice during their post-cancer life-course.
Données utilisées
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Justification du recours à cette(ces) variable(s) sensible(s)
Description of the study population
Recours au numéro d'identification des professionnels de santé
Plateforme utilisée pour l'analyse des données
Acteurs finançant et participant à l'étude
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Type de responsable de traitement 1
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Calendrier du projet
Base légale pour accéder aux données
Encadrement réglementaire
Destinataire(s) des données
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Durée de conservation aux fins du projet (en années)
8
Existence d'une prise de décision automatisée
Fondement juridique
Article 6 du RGPD (Licéité du traitement)
Article 9 du RGPD (Exception permettant de traiter des données de santé)
Transfert de données personnelles vers un pays hors UE
Droits des personnes
IARC/WHO processes personal data in accordance with the UN Principles and the IARC Data Protection Policy. IARC/WHO is committed to strive for the highest level of protection as it processes personal data, and will always respect the rights and freedoms of data subjects, such as the right to access, the right to rectification, right to erasure, right to restriction of processing, right to data portability. Where IARC/WHO, as data controller, is not in a position to identify the data subject, IARC/WHO will be able to provide data subject rights where the data subject, for the purpose of exercising his or her rights under the IARC Data Protection Policy, provides additional information enabling his or her identification.