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一个验证的预后指数,预测对去势抵抗性前列腺癌的地塞米松和己烯雌酚的反应。

A validated prognostic index predicting response to dexamethasone and diethylstilbestrol in castrate-resistant prostate cancer.

机构信息

Department of Medical Oncology, Barts and the London National Health Service Trust, London, United Kingdom.

出版信息

Cancer. 2010 Aug 1;116(15):3595-602. doi: 10.1002/cncr.25194.

Abstract

BACKGROUND

The objective of this study was to identify subgroups of patients with castrate-resistant prostate cancer (CRPC) who had a prolonged response to combined dexamethasone and diethylstilbestrol (DS) therapy by constructing a prognostic index.

METHODS

Multivariate and cutoff point analyses with bootstrapping were performed 1 month after commencing DS therapy, and data were validated using an independent external dataset.

RESULTS

The median overall survival for 145 patients was 18.3 months (95% confidence interval [CI], 15.4-23.3 months). Only 2 factors were significant on multivariate analysis: a prostate-specific antigen (PSA) level below the median at the start of DS therapy and a decline>50% in the PSA level after 1 month on DS therapy. Subsequent cutoff point analyses revealed that a PSA level<88 ng/mL at the start of DS therapy and a reduction>53.1% in PSA after the first month of treatment were the most significant factors. These 2 factors were used to construct a prognostic index, which was validated successfully by the external dataset (median overall survival, 18.3 months [95% CI, 16.4-28.0 months]; concordance, 72% [95% CI, 68%-76%]). The prognostic index identified 3 prognostic groups: The 2-year overall survival rate for these 3 groups was 68% (95% CI, 57%-98%) for the good prognostic group, 40% (95% CI, 31%-52%) for the intermediate prognostic group, and 12% (95% CI, 5%-25%) for the poor prognostic group.

CONCLUSIONS

The easy-to-use prognostic index that the authors developed was able to identify a subgroup of patients with CRPC who had prolonged survival only 1 month after starting DS therapy.

摘要

背景

本研究的目的是通过构建预后指数来确定接受联合地塞米松和己烯雌酚(DS)治疗的去势抵抗性前列腺癌(CRPC)患者中对治疗有延长反应的亚组。

方法

在开始 DS 治疗后 1 个月进行多变量和截断点分析,并使用独立的外部数据集进行验证。

结果

145 例患者的中位总生存期为 18.3 个月(95%置信区间[CI],15.4-23.3 个月)。只有 2 个因素在多变量分析中具有显著性:DS 治疗开始时前列腺特异性抗原(PSA)水平低于中位数和 DS 治疗 1 个月后 PSA 水平下降>50%。随后的截断点分析显示,DS 治疗开始时 PSA<88ng/mL 和治疗第一个月 PSA 降低>53.1%是最重要的因素。这两个因素被用于构建预后指数,该指数在外数据集得到了成功验证(中位总生存期,18.3 个月[95%CI,16.4-28.0 个月];一致性,72%[95%CI,68%-76%])。该预后指数确定了 3 个预后组:这 3 组的 2 年总生存率分别为:预后良好组为 68%(95%CI,57%-98%)、中间预后组为 40%(95%CI,31%-52%)和预后不良组为 12%(95%CI,5%-25%)。

结论

作者开发的易于使用的预后指数能够在开始 DS 治疗后仅 1 个月就识别出 CRPC 患者的亚组,这些患者的生存时间延长。

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