Ternant, David http://orcid.org/0000-0003-4020-4545
Pfister, Marc
Le Tilly, Olivier
Mulleman, Denis
Picon, Laurence
Willot, Stéphanie
Passot, Christophe
Bejan-Angoulvant, Theodora
Lecomte, Thierry
Paintaud, Gilles
Koch, Gilbert
Article History
Accepted: 6 July 2021
First Online: 5 August 2021
Declarations
:
: This study was partly supported by the Higher Education and Research Ministry under the programme ‘Investissements d’avenir’ Grant Agreement: LabEx MAbImprove ANR-10-LABX-53-01.
: David Ternant acted as a consultant and has given lectures on behalf of his institution for Amgen, Sanofi, Boehringer-Ingelheim and Novartis. Marc Pfister is a part-time consultant at Certara, outside the submitted work. Denis Mulleman has acted as a consultant and given lectures on behalf of his institution for Pfizer, Novartis and Grifols; he has been invited to attend an international congress by Janssen-Cilag. His institution received grants for research from the non-governmental organisation Lions Club Tours Val de France. Laurence Picon has acted as a consultant for Abbvie, Janssen-Cilag, Pfizer and Takeda, outside the submitted work. Stephanie Willot has given lectures to Abbvie, outside the submitted work. Theodora Bejan-Angoulvant reports support for travel to congresses from Servier and BMS, outside the submitted work. She has given lectures on behalf of her institution to Amgen and Sanofi, outside the submitted work. Gilles Paintaud has received grants for his research team from Roche Pharma, Chugai, Pfizer, Novartis and Sanofi-Genzyme. Olivier le Tilly, Christophe Passot, Thierry Lecomte and Gilbert Koch have no conflicts of interest that are directly relevant to the content of this article.
: Ethical approval was not sought in this retrospective analysis of routine patients, which is in accordance with institutional guidelines.
: Informed consent was not sought in this retrospective analysis of routine patients, which is in accordance with institutional guidelines.
: Not applicable.
: Data and material are available on request to the corresponding author.
: The code is available on request to the corresponding author.
: DT designed the research, analysed the data, interpreted the results and wrote the manuscript. MP, GP and GK participated in the data analysis and interpretation of the results and reviewed the manuscript. OT contributed to the data analysis and interpretation of the results and reviewed the manuscript. DM, LP, SW CP and TL participated in the data acquisition and reviewed the manuscript.