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
. 2011 Jun;12(3):173-9.
doi: 10.1007/s11934-011-0187-z.

Current clinical trials in castrate-resistant prostate cancer

Affiliations
Review

Current clinical trials in castrate-resistant prostate cancer

Daniel P Petrylak. Curr Urol Rep. 2011 Jun.

Abstract

Seven years passed since docetaxel/prednisone demonstrated and overall survival benefit, leading to its approval by the FDA for metastatic castration resistant prostate cancer. In 2010, two new treatments, sipuleucel-T and cabazitaxel, were approved by the United States Food and Drug Administration for men with castration-resistant prostate cancer, based upon improvement in overall survival. The progress that has been made in understanding the biological basis of disease progression, particularly the role of the continued activation of the androgen receptor, have led to new treatments that will further improve survival in these patients. Abiraterone, a drug that depletes both intracellular and extracellular sources of testosterone, demonstrated a 3.9-month improvement in survival in patients who failed docetaxel-based chemotherapy. Other drugs targeting the androgen-receptor axis, such as TAK-700 and MDV3100, have demonstrated significant activity in phase 1 and 2 studies, and are currently in phase 3. Agents that target angiogenesis, bone, and novel apoptotic proteins currently are under investigation, either as single agents or in combination with chemotherapy. The challenge for the development of clinical trials will be how these compounds will be sequenced in the future.

PubMed Disclaimer

References

    1. BJU Int. 2010 Oct;106(7):966-73 - PubMed
    1. Cancer Biol Ther. 2009 Nov;8(22):2153-9 - PubMed
    1. Clin Cancer Res. 2008 Oct 1;14(19):6270-6 - PubMed
    1. J Clin Oncol. 2010 Sep 20;28(27):4247-54 - PubMed
    1. N Engl J Med. 2004 Oct 7;351(15):1513-20 - PubMed

MeSH terms

LinkOut - more resources