What is the current status of second-line chemotherapy for castration-resistant prostate cancer?

被引:0
作者
Rosenberg, Jonathan E. [1 ,2 ]
Oh, William K. [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02446 USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
来源
NATURE CLINICAL PRACTICE UROLOGY | 2008年 / 5卷 / 12期
关键词
chemotherapy; chemotherapy resistance; mitoxantrone; prostate cancer; salvage treatment;
D O I
10.1038/ncpuro1232
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Patients with castration-resistant prostate cancer (CRPC) who show progression of disease after first-line chemotherapy with docetaxel have few proven treatment options. Mitoxantrone plus prednisone is frequently used in this setting. The retrospective analysis by Berthold et al. of mitoxantrone after first-line docetaxel in patients with CRPC suggests that mitoxantrone has a modest level of activity in this setting, with a second-line PSA response rate of 15% and a median time to PSA progression of 3.2 months. Patients with CRPC treated with docetaxel after progression on first-line mitoxantrone had a PSA response rate of 28% and a median time to PSA progression of 5.9 months. In this analysis, median survival of patients was 10 months and did not differ according to choice of first-line agent. Mitoxantrone therapy can be considered in select patients after failure of first-line docetaxel, and vice versa. Other cytotoxic agents such as carboplatin might have a limited role in this patient population. In general, patients with CRPC should be directed towards clinical trials, when available.
引用
收藏
页码:650 / 651
页数:2
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