Timmerman, Laura M. http://orcid.org/0000-0002-2848-1681
Hensen, Lobke C. M. http://orcid.org/0000-0002-6207-5556
van Eijs, Mick J. M. http://orcid.org/0000-0002-9763-6704
Verheijden, Rik J. http://orcid.org/0000-0003-1966-1063
Suijkerbuijk, Karijn P. M. http://orcid.org/0000-0003-3604-5430
Meyaard, Linde http://orcid.org/0000-0003-0707-4793
van der Vlist, Michiel http://orcid.org/0000-0003-0931-8982
,
Meyaard, Linde
Kuball, Jürgen H. E.
Oldenburg, Bas
Leusen, Jeanette H. W.
Funding for this research was provided by:
Oncode Institute, which is partly funded by the Dutch Cancer Society
Article History
Received: 8 May 2024
Accepted: 13 June 2024
First Online: 5 July 2024
Declarations
:
: KPMS has advisory relationships with Sairopa, Pierre Fabre, AbbVie, and received research funding from Bristol-Myers Squibb, Genmab, Philips and TigaTx. All paid to institution. LM’s research laboratory at UMC Utrecht has received research funding from NextCure, NGM Biopharmaceuticals, Boehringer Ingelheim and argenx and has received consultancy fees from Eli Lilly, Third Rock Ventures and Abbvie. LM has not received personal fees or other personal benefits. MV’s research lab at UMC Utrecht has received research funding from Boehringer Ingelheim and argenx. MV has not received personal fees or other personal benefits.
: We confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. The UNICIT biobank study was not considered subject to the Dutch Medical Research with Human Subjects Law by the Medical Research Ethics Committee of the University Medical Center Utrecht. The Biobank Review Committee of the University Medical Center Utrecht gave ethical approval for the UNICIT biobank study (Toetsingscommissie biobanken TC-bio 18-123; biobank protocol) and granted permission for use of human biospecimens for the present study oetsingscommissie biobanken TC-bio 19-704; release review protocol).
: We confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.