An update on androgen deprivation therapy for prostate cancer

被引:133
作者
Sharifi, Nima [1 ]
Gulley, James L. [2 ,3 ]
Dahut, William L. [2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Div Hematol & Oncol, Dept Internal Med, Dallas, TX 75390 USA
[2] NCI, Med Oncol Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[3] NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
GONADOTROPIN-RELEASING-HORMONE; RANDOMIZED CONTROLLED-TRIAL; PREVENT BONE LOSS; I CLINICAL-TRIAL; ABIRATERONE ACETATE; CARDIOVASCULAR MORTALITY; ANTITUMOR-ACTIVITY; INTERIM ANALYSIS; ANTIGEN DECLINE; ZOLEDRONIC ACID;
D O I
10.1677/ERC-10-0187
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Androgen deprivation therapy (ADT) with gonadal testosterone depletion is the frontline treatment for advanced prostate cancer. Other hormonal interventions have a role in the treatment of prostate cancer. We sought to examine systematically the evidence for hormonal interventions in prostate cancer, risks of ADT, and interventions that mitigate these risks. Search results for therapeutic studies were focused primarily on randomized controlled clinical trials, and the Jadad scale criteria were used to evaluate the quality of these studies. Four trials of the efficacy of intermittent ADT versus continuous ADT were included. One randomized study analysis and six postrandomization analyses were included on the effects of ADT on cardiovascular mortality. Seven randomized controlled trials of pharmacologic interventions were included for the treatment of metabolic effects due to ADT. One randomized trial of GnRH antagonist versus GnRH agonist was included. Six phase I/II clinical trials of secondary hormonal therapies with novel mechanisms of action were included. Randomized studies completed to date indicate that intermittent ADT might be equivalent to continuous ADT. Although adverse effects of ADT include risk factors for cardiovascular disease, effects on cardiovascular mortality are uncertain. Bone loss and increased risk of fracture may be effectively treated with pharmacologic interventions. Benefits of ADT must be balanced with a consideration of the risks. Endocrine-Related Cancer (2010) 17 R305-R315
引用
收藏
页码:R305 / R315
页数:11
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