Griesshammer, Martin
von der Heyde, Eyck
Schlag, Rudolf
Schmidt, Burkhard
Weniger, Steffi
Koenigsmann, Michael
Stauch, Martina
Gückel, Eva
Baum, Volker
Weide, Rudolf
Funding for this research was provided by:
Universitätsklinikum Knappschaftskrankenhaus Bochum GmbH
Article History
Received: 22 October 2025
Accepted: 9 March 2026
First Online: 12 May 2026
Declarations
:
: The study was approved by the ethics committees at each study site (leading ethics committee: “Ärztekammer Westfalen-Lippe und der Westfälischen Wilhelms Universität” responsible for the scientific expert (Prof. Griesshammer) was consulted before commencement of this study [positive vote on 13-May-2015]). The study was conducted in accordance with all local legal and regulatory requirements, as well as the general principles set forth in the International Ethical Guidelines for Biomedical Research Involving Human Patients, Guidelines for Good Clinical Practice, and the Declaration of Helsinki. All patients provided written informed consent prior to study inclusion.
: Not applicable for patients.
: Martin Griesshammer: Participated in advisory boards for and received grant support, consulting fees, honoraria, and meeting and travel support from Amgen, AOP Health, Eli Lilly, Novartis, BMS, AstraZeneca, and Janssen. Eyck von der Heyde: Received consulting fees and honoraria from Novartis, BMS, AstraZeneca, Ipsen, BeiGene, Iomedico, Boehringer Ingelheim and PierreFabre. Burkhard Schmidt: Participated in advisory boards and received honoraria and meeting and travel support from AbbVie, AOP, AstraZeneca, Beigene, BMS, Hexal, Incyte, Janssen, Menari Stemline, Novartis, Pfizer, Sanofi and SoBi Eva Gückel: Employee of Novartis Pharma, Germany. Volker Baum: Employee of Novartis Pharma, Germany The remaining authors declared no competing interests.