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Satraplatin for hormone-refractory prostate cancer.

机译:沙铂治疗激素难治性前列腺癌。

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摘要

Satraplatin, which is currently awaiting approval by the US Food and Drug Adminstration, significantly decreased the risk for disease progression in a phase III trial in hormone-refractory prostate cancer (HRPC), according to a study presented at the 3rd Prostate Cancer Symposium (Orlando, FL, USA; Feb 22-24, 2007). 950 patients who had failed treatment with at least one previous regimen were randomised to receive prednisone plus satraplatin, or placebo. Patients treated with satraplatin had a 40% decrease in the risk of disease progression compared with those in the placebo group. The improvement in progression-free survival (PFS) increased over time. At the median time, PFS was 11 weeks and 10 weeks in the satraplatin and placebo groups, respectively. At the 75th percentile, PFS improved by 89% (36 vs 19 weeks). After 6 months, 30% of the satraplatin and 17% of the placebo group had not progressed; and at 12 months, nonprogression was 16% and 7%, respectively.
机译:根据第三届前列腺癌专题讨论会(奥兰多)上发表的一项研究,目前正在等待美国食品和药物管理局批准的Satraplatin大大降低了激素难治性前列腺癌(HRPC)的III期临床试验中疾病进展的风险。 ,美国佛罗里达; 2007年2月22日至24日)。 950名在至少一种既往治疗方案下治疗失败的患者被随机分配接受泼尼松联合沙铂或安慰剂治疗。与安慰剂组相比,使用沙铂治疗的患者疾病进展的风险降低了40%。随着时间的推移,无进展生存期(PFS)的改善有所增加。在中位时间,沙铂和安慰剂组的PFS分别为11周和10周。在第75个百分点,PFS改善了89%(36对19周)。 6个月后,沙铂的30%和安慰剂组的17%没有进展;在12个月时,不进步度分别为16%和7%。

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