Funding for this research was provided by:
Association pour la Recherche et l’Information Scientifique et Thérapeutique en Oncologie Thoracique (ARISTOT).
Received: 8 August 2022
Accepted: 9 May 2023
First Online: 23 June 2023
: This study was approved by our institutional review board, respecting reference methodology No. 004 (MR004), which concerns research not involving human subjects (studies and evaluations in the health field). Study ethics approval was obtained on 01 september 2021 (Comité d’Ethique des Centres d’Investigation Clinique Rhône-Alpes-Auvergne, Clermont-Ferrand, IRB 5891). At the time of this study, French law did not require the consent of participants, since no intervention was evaluated (Commission nationale de l’informatique et des libertés law of June 20 2018 number 2018 − 493, NOR : JUSC1732261L, Journal Officiel de la République Française number 0141, June 21 2018). An information and non-objection letter has been sent to living patients in the cohort. All relevant permissions were obtained to access the raw data and all methods were performed in accordance with the relevant guidelines and regulations.
: Not applicable.
: HP, SB, SC, PB have nothing to disclose. ACT received personal fees and non-financial support from Astra Zeneca, BMS, MSD, Novartis, Boehringer Ingelheim, Roche, Pfizer. DMS received grants from Roche, Astra Zeneca, BMS, Boehringer Ingelheim, Abbvie, Pfizer; received personal fees from Roche, Astra Zeneca, BMS, MSD, Lilly, Takeda, Boehringer Ingelheim, Abbvie, Becton Dickinson, Pfizer, Novartis; received non-financial support from Roche, Astra Zeneca, BMS, MSD, Lilly, Takeda, Boehringer Ingelheim and Pfizer.