Dalle, Stéphane
Mortier, Laurent
Corrie, Pippa
Lotem, Michal
Board, Ruth
Arance, Ana María
Meiss, Frank
Terheyden, Patrick
Gutzmer, Ralf
Buysse, Brian
Oh, Kelly
Brokaw, Jane
Le, T. Kim
Mathias, Susan D.
Scotto, Julie
Lord-Bessen, Jennifer
Moshyk, Andriy
Kotapati, Srividya
Middleton, Mark R.
Funding for this research was provided by:
This work was supported by Bristol Myers Squibb (no grant number is applicable).
Article History
Received: 20 November 2020
Accepted: 15 March 2021
First Online: 29 May 2021
Declarations
:
: This study was approved by the institutional review board/ethics committee at each participating centre (Additional file InternalRef removed) and was conducted in accordance with the Declaration of Helsinki and International Society for Pharmacoepidemiology Guidelines for Good Epidemiology Practices. Patients generally provided written consent for enrollment, but they could have provided verbal consent documented by the site staff if in accordance with local regulations and the institutional review board /ethics committee.
: Not applicable.
: SD has received institutional research grants from Bristol Myers Squibb and Merck Sharp & Dohme, and travel support from Bristol Myers Squibb. LM has received personal fees for French Medical Board expenses and congress travel support from Bristol Myers Squibb and Roche. PC has served on advisory boards, received speaker fees, and received institutional research support from Bristol Myers Squibb, Merck Sharp & Dohme, and Novartis. ML declares no conflicts to disclose. RB reports personal fees from Bristol Myers Squibb. AMA has served as an advisor, consultant, and speaker for Amgen, Bristol Myers Squibb, Merck Sharp & Dohme, Novartis, Pierre Fabre, Roche, and Sanofi. FM has served as an advisor to Bristol Myers Squibb, Novartis, Pierre Fabre, Roche, and Sanofi-Aventis; has served as a speaker for Merck Sharp & Dohme; and has received travel support from Bristol Myers Squibb, Novartis, Pierre Fabre, Roche, and Sanofi-Aventis. PT has worked as a consultant to Bristol Myers Squibb, Merck Serono, Novartis, Pierre Fabre, Roche, and Sanofi; has served as a speaker for Bristol Myers Squibb, CureVac, Merck Sharp & Dohme, Novartis, Pierre Fabre, and Roche; and has received travel support from Bristol Myers Squibb, and Pierre Fabre. RG has worked as an advisor to Almitall Hermal, Amgen, Bristol Myers Squibb, 4SC, Merck Serono, Merck Sharp & Dohme, Novartis, Pierre Fabre, Pfizer, Sanofi Regeneron, Sun Pharma, and Roche; has served as a speaker for Almitall Hermal, Amgen, Bristol Myers Squibb, Merck Serono, Merck Sharp & Dohme, Novartis, Pierre Fabre, Pfizer, Sanofi Regeneron, Sun Pharma, and Roche; has received meeting support from Bristol Myers Squibb, Merck Serono, Pierre Fabre, and Roche; and has received institutional research support from Bristol Myers Squibb. BB and KO are employees of Syneos Health, the contract research organisation that conducted the study including data collection and statistical analysis, but were not compensated for authorship. JB was an employee of Bristol Myers Squibb at the time of this study. TKL is an employee of Bristol Myers Squibb. SDM declares no conflicts to disclose. JS and SK are employees of Bristol Myers Squibb. JL and AM are employees of and stockholders in Bristol Myers Squibb. MRM has served as an advisor to Amgen, Array Biopharma, BiolineRx, Bristol Myers Squibb, GlaxoSmithKline, Immunocore, Kineta, Novartis, Rigontec, and Silicon Therapeutics; has received institutional research support from Array Biopharma, AstraZeneca, BiolineRx, Bristol Myers Squibb, Eisai, GlaxoSmithKline, Immunocore, Merck, Merck Sharp & Dohme, Millennium, Novartis, Pfizer, Regeneron, Replimune, Rigontec, and Roche; has received travel support from Immunocore, Merck, Merck Sharp & Dohme, and Replimune; and is a member of the Independent Data Safety Monitoring Committee for Eisai and Merck/Merck Sharp & Dohme.