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Article History

Received: 13 January 2023

Accepted: 8 May 2023

First Online: 5 June 2023

Declarations

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: Agmal Scherzad, Manuel Stöth, Till J. Meyer, Lukas Haug, Thomas Gehrke, Svenja Meierjohann, Matthias Scheich, Rudolf Hagen and Stephan Hackenberg have no conflicts of interest to declare that are relevant to the content of this article. B. Schilling is on the advisory board or has received honoraria from Almirall, Pfizer, Sanofi, Incyte, Novartis, Roche, Bristol-Myers Squibb and MSD Sharp & Dohme, research funding from Novartis, Pierre Fabre Pharmaceuticals, Bristol-Myers Squibb and MSD Sharp & Dohme and travel support from Novartis, Roche, Bristol-Myers Squibb, Pierre Fabre Pharmaceuticals, MSD Sharp & Dohme and Amgen, outside the submitted work. A. Gesierich received speaker´s honoraria from Almirall, Bristol-Myers Squibb, MSD Sharp & Dohme and Roche; intermittent advisory board relationships with Amgen, Bristol-Myers Squibb, Novartis, MSD Sharp & Dohme, Pierre Fabre Pharmaceuticals, Pfizer, Roche and Sanofi Genzyme; travel and congress fee support from Bristol-Myers Squibb, MSD Sharp & Dohme, Novartis, Pierre Fabre Pharmaceuticals and Roche. Clinical studies: Amgen, Array, Bristol-Myers Squibb, GSK, Novartis, Merck, MSD Sharp & Dohme, Pfizer and Roche.

: This study protocol was reviewed and approved by the ethics committee of the medical faculty of the Julius-Maximilians-University Würzburg, approval number 2020110301. Patient informed consent was waived due to the study’s retrospective nature, taking into account the national legal bases. Data collection and publication were carried out in compliance with the guidelines for ensuring good scientific practice and in accordance with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Only data generated in compliance with relevant legal requirements and professional ethics were evaluated. The applicable data protection regulations and the institute's internal guidelines for handling patient data were observed.