Müller, Lukas
Gairing, Simon Johannes
Kloeckner, Roman
Foerster, Friedrich
Schleicher, Eva Maria
Weinmann, Arndt
Mittler, Jens
Stoehr, Fabian
Halfmann, Moritz Christian
Düber, Christoph
Galle, Peter Robert
Hahn, Felix https://orcid.org/0000-0001-5122-9014
Funding for this research was provided by:
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Article History
Received: 4 May 2022
Accepted: 31 August 2022
First Online: 24 September 2022
Declarations
:
: The ethics committee of the Medical Association of Rhineland Palatinate, Mainz, Germany, approved this study (permit number 837.199.10). The requirement for informed consent was waived for the retrospective analysis of clinical data.
: Not applicable.
: RK reports personal fees from Boston Scientific, personal fees from Bristol-Myers Squibb, personal fees from Guerbet, personal fees from SIRTEX, personal fees from Roche, personal fees from BTG, personal fees from Ipsen, personal fees from Siemens, personal fees from MSD - Merck Sharp & Dohme. FF reports receiving consulting and lectures fees from Roche; lectures fees from Lilly and Pfizer. AW received compensations as a member of scientific advisory boards for Bayer, BMS, Eisai, and Sanofi and served as a speaker for Leo Pharma, Eisai, Ipsen, and Roche and received travel support from Merck and Servier. PRG reports receiving consulting and lectures fees from Adaptimmune, AstraZeneca, Bayer, BMS, Boston Scientific, Eisai, Guerbet, Ipsen, Lilly, MSD, Roche, Sirtex. None of these influenced the conduction of this study. None of the other authors reports a conflict of interest.