Houpert, Rémi http://orcid.org/0000-0001-6479-4135
Almont, Thierry
Belahreche, Rostom
Faro, Mamadi
Okouango, Jennie
Vestris, Mylène
Macni, Jonathan
Pierre-Louis, Olivier
Montabord, Christelle
Beaubrun-Renard, Murielle
Soumah, Naby
Boisseau, Martial
Véronique-Baudin, Jacqueline
Joachim, Clarisse
Article History
Received: 24 May 2023
Accepted: 22 November 2023
First Online: 6 December 2023
Declarations
:
: The cancer registry of Martinique is authorized by the French Data Protection Authority, Commission National Informatique et Liberté (CNIL), authorization N° 987001 of november 16, 1987. (Date of last CNIL amendment: June 05, 2015) Given their public health mandate, French cancer registries are authorized by the French Data Protection Authority “Commission National Informatique et Liberté” (CNIL), to collect data on cancer cases with a waiver for written informed consent (CNIL deliberation n°03–053 of November 27, 2003). Patients’ information is given by notices displayed in health care facilities, their attending physician or specialist. General information is also available on the National Cancer Institute website: ExternalRef removed. This study obtained ethics approval from the research ethic committee of the Comité de Protection des Personnes Ile de France IV Institutional Review Board Agreement of US Department of Health and Human Services, N°IRB 00003835. The Privacy Impact Assessment (PIA) was votted by the data protection ofcer of the University Hospital of Martinique (dpo@chu-martinique.fr) in accordance to the General Data Protection Regulation (GDPR). The study was performed in accordance with the Declaration of Helsinki.
: Not applicable. Consent for publication was not required since our project do not involve patients.
: The authors declare no competing interests.