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Authors
Jansen, Lina
Hermann, Silke
Bergbold, Susanne
Arndt, Volker
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Funding
Funding for this research was provided by:
Deutsches Krebsforschungszentrum (DKFZ)
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Article History
Received: 14 May 2024
Accepted: 1 October 2024
First Online: 22 October 2024
Declarations
:
: The authors declare no competing interests.
: Data collection within the cancer registry has been carried out according to the Cancer Registry Act of Baden-Württemberg. The notifying physician must inform the patient of the content of the notification and the further processing and use of his/her data by the authorities named in the Cancer Registry Act by handing out an information sheet and documenting the information in text form. The patient is informed that he/she has the right to object [§ 4 (2)]. The epidemiological cancer registry Baden-Württemberg is allowed to use the data for clinical-epidemiological analyses [§ 6 (2), § 7 (1)]. Due to the regulations in the Cancer Registry Act of Baden-Württemberg and as only anonymized data were used for the analyses, approval of an Ethical Committee is not necessary. The study was conducted in accordance with the recommendations of the Declaration of Helsinki by the World Medical Association.
