Literature DB >> 16515496

Controversies of androgen ablation therapy for metastatic prostate cancer.

Shandra S Wilson1, E David Crawford.   

Abstract

Ever since Huggins and Hodges won a Nobel Prize in 1966 for their work describing the relationship between testosterone and prostate cancer, androgen deprivation has continued to be an important component in the treatment of prostate cancer. Refinements in the therapy have occurred in the past 50 years, yet controversies still exist. This review details the controversies and advances in androgen deprivation for prostate cancer including: neoadjuvant androgen deprivation, combined androgen blockade, early versus late androgen deprivation treatment, intermittent versus continuous androgen deprivation monotherapy, anti-androgen monotherapy, anti-androgen and 5-alpha reductase inhibitor combinations, androgen deprivation with periodic intravenous bisphosphonate infusions, and androgen deprivation in conjunction with chemotherapy.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16515496     DOI: 10.2174/138161206776056056

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  3 in total

Review 1.  The diverse and contrasting effects of using human prostate cancer cell lines to study androgen receptor roles in prostate cancer.

Authors:  Sheng-Qiang Yu; Kuo-Pao Lai; Shu-Jie Xia; Hong-Chiang Chang; Chawnshang Chang; Shuyuan Yeh
Journal:  Asian J Androl       Date:  2008-12-22       Impact factor: 3.285

2.  Expression and colocalization of β-catenin and lymphoid enhancing factor-1 in prostate cancer progression.

Authors:  Tyler M Bauman; Chad M Vezina; Emily A Ricke; Richard B Halberg; Wei Huang; Richard E Peterson; William A Ricke
Journal:  Hum Pathol       Date:  2016-01-19       Impact factor: 3.466

Review 3.  Should finasteride be used to prevent prostate cancer?

Authors:  Neil Fleshner; Girish Kulkarni
Journal:  Curr Treat Options Oncol       Date:  2006-09
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.