Phase II study evaluating oral triamcinolone in patients with androgen-independent prostate cancer
详细信息    查看全文
文摘

Objectives

To assess the effect of triamcinolone administration on the serum prostate-specific antigen (PSA) response and the time to progression in patients with androgen-independent prostate cancer (AIPC).

Methods

Patients with AIPC were prospectively treated with oral triamcinolone 4 mg twice daily, and their serum PSA and cortisol levels were measured monthly. Patients with greater than 25 % increases in serum PSA from baseline were considered to have progressive disease and were removed from the study. Those patients who had a decrease in serum PSA levels or stable disease continued in the study until disease progression. Bone scans were obtained every 12 weeks and at progression.

Results

Twenty-four patients with AIPC were treated from November 2002 to June 2004. A partial response with a more than 50 % decrease in serum PSA level was seen in 29 % . Another 21 % achieved stable disease. No statistically significant difference was found in the time to progression in the partial responders and patients with stable disease. The median time to progression in both groups was 7.5 months. Treatment was well tolerated without any grade 3 or 4 toxicity.

Conclusions

Oral triamcinolone was well tolerated by patients with AIPC, with 50 % of the patients exhibiting a good response to therapy in terms of serum PSA level and time to progression.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700