Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Feb;52(2):219-25.
doi: 10.1007/s00120-012-3054-8.

[Pathophysiology and therapy of castration-resistant prostate cancer]

[Article in German]
Affiliations
Review

[Pathophysiology and therapy of castration-resistant prostate cancer]

[Article in German]
A S Merseburger et al. Urologe A. 2013 Feb.

Abstract

Advanced prostate cancer that progresses under androgen deprivation therapy has long been thought to be refractory to further hormonal treatment. The identification of the mechanism of cancer cells has revolutionized this understanding. Today it is known that castration-resistant prostate cancer (CRPC) still receives signals through the androgen receptor transduction pathways and furthermore is sensitive to hormone therapy. New substances, such as abiraterone, enzalutamide (MDV3100) and TAK 700 target these mechanisms of resistance of cancer cells, stop testosterone production and show not only better tolerance but also effective antitumor activity. Due to the heterogeneity of tumors with cells in varying states of differentiation, the treatment of CRPC with androgen deprivation therapy remains a cornerstone of disease management. To what extent the experimental findings and the recommendations in the guidelines are put into practice was the subject of a survey among urologists analyzing their treatment strategies with CRPC patients.

PubMed Disclaimer

References

    1. Oncogene. 2003 Feb 6;22(5):734-9 - PubMed
    1. J Clin Oncol. 2002 Jul 1;20(13):3001-15 - PubMed
    1. Cancer Res. 2010 Oct 15;70(20):7992-8002 - PubMed
    1. Lancet. 2010 Apr 24;375(9724):1437-46 - PubMed
    1. Clinics (Sao Paulo). 2012;67(4):389-94 - PubMed

MeSH terms

LinkOut - more resources