Bergmann, Lina
Greimeier, Sarah
Riethdorf, Sabine
Rohlfing, Tina
Kaune, Moritz
Busenbender, Tobias
Strewinsky, Nadja
Dyshlovoy, Sergey
Joosse, Simon
Peine, Sven
Pantel, Klaus
von Amsberg, Gunhild
Werner, Stefan
Funding for this research was provided by:
Universitätsklinikum Hamburg-Eppendorf (UKE)
Article History
Received: 19 December 2024
Accepted: 17 March 2025
First Online: 3 April 2025
Declarations
:
: Blood samples were collected from patients with mPC at the University Medical Center Hamburg-Eppendorf in accordance with the Declaration of Helsinki and approved by the Ethics Committee of the City of Hamburg (Hamburger Ärztekammer, PV5392). All patients gave informed consent.
: All authors read and approved the final manuscript.
: Gunhild von Amsberg is consultant or advisor of Amgen, Roche, BMS, Astellas, Sanofi, Janssen, MSD, Ipsen, Pfizer, AstraZeneca, Merck, EISAI, Bayer. The other authors declare no potential conflicts of interest.
: Blood-based biomarkers of metastatic prostate cancer are urgently needed to identify patients with progression to aggressive and androgen-independent disease, and to monitor treatment response and emerging therapy resistance. We have developed a convenient PCR-based method to identify neuroendocrine prostate cancers based on their gene expression in circulating tumor cells. This test allows clinical monitoring of patients under androgen receptor-directed treatment and enables the early identification of progression to androgen-independent and therapy-induced neuroendocrine prostate cancer. In this way, suitable treatment strategies can be applied at an early stage before clinical symptoms and deterioration of general condition have occurred.