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Prognostic Index Model for Progression-Free Survival in Chemotherapy-Naïve Metastatic Castration-Resistant Prostate Cancer Treated With Abiraterone Acetate Plus Prednisone.醋酸阿比特龙联合泼尼松治疗初治转移性去势抵抗性前列腺癌无进展生存期的预后指数模型
Clin Genitourin Cancer. 2017 Jul 25. doi: 10.1016/j.clgc.2017.07.014.
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Management of Patients with Advanced Prostate Cancer: The Report of the Advanced Prostate Cancer Consensus Conference APCCC 2017.晚期前列腺癌患者的管理:2017 年晚期前列腺癌共识会议(APCCC)报告。
Eur Urol. 2018 Feb;73(2):178-211. doi: 10.1016/j.eururo.2017.06.002. Epub 2017 Jun 24.
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Clinical outcomes and survival surrogacy studies of prostate-specific antigen declines following enzalutamide in men with metastatic castration-resistant prostate cancer previously treated with docetaxel.恩杂鲁胺治疗后,转移性去势抵抗性前列腺癌患者(此前接受多西他赛治疗)前列腺特异性抗原下降的临床结局和生存替代研究
Cancer. 2017 Jun 15;123(12):2303-2311. doi: 10.1002/cncr.30587. Epub 2017 Feb 7.
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Enzalutamide in Men with Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer: Extended Analysis of the Phase 3 PREVAIL Study.恩杂鲁胺用于未经化疗的转移性去势抵抗性前列腺癌男性患者:3期PREVAIL研究的扩展分析
Eur Urol. 2017 Feb;71(2):151-154. doi: 10.1016/j.eururo.2016.07.032. Epub 2016 Jul 28.
5
Meta-Analysis Evaluating the Impact of Site of Metastasis on Overall Survival in Men With Castration-Resistant Prostate Cancer.评估转移部位对去势抵抗性前列腺癌男性患者总生存期影响的Meta分析
J Clin Oncol. 2016 May 10;34(14):1652-9. doi: 10.1200/JCO.2015.65.7270. Epub 2016 Mar 7.
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A prognostic index model for predicting overall survival in patients with metastatic castration-resistant prostate cancer treated with abiraterone acetate after docetaxel.一种用于预测多西他赛后接受醋酸阿比特龙治疗的转移性去势抵抗性前列腺癌患者总生存期的预后指数模型。
Ann Oncol. 2016 Mar;27(3):454-60. doi: 10.1093/annonc/mdv594. Epub 2015 Dec 18.
7
Plasma AR and abiraterone-resistant prostate cancer.血浆雄激素受体与阿比特龙耐药性前列腺癌
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Cell. 2015 May 21;161(5):1215-1228. doi: 10.1016/j.cell.2015.05.001.
9
Abiraterone acetate plus prednisone versus placebo plus prednisone in chemotherapy-naive men with metastatic castration-resistant prostate cancer (COU-AA-302): final overall survival analysis of a randomised, double-blind, placebo-controlled phase 3 study.醋酸阿比特龙联合泼尼松对比安慰剂联合泼尼松治疗化疗初治转移性去势抵抗性前列腺癌患者(COU-AA-302):一项随机、双盲、安慰剂对照的 3 期研究的最终总生存分析。
Lancet Oncol. 2015 Feb;16(2):152-60. doi: 10.1016/S1470-2045(14)71205-7. Epub 2015 Jan 16.
10
AR-V7 and resistance to enzalutamide and abiraterone in prostate cancer.AR-V7 与前列腺癌中对恩杂鲁胺和阿比特龙的耐药性。
N Engl J Med. 2014 Sep 11;371(11):1028-38. doi: 10.1056/NEJMoa1315815. Epub 2014 Sep 3.

开发和验证化疗初治转移性去势抵抗性前列腺癌男性患者总生存期的预后模型。

Development and validation of a prognostic model for overall survival in chemotherapy-naïve men with metastatic castration-resistant prostate cancer.

机构信息

Division of Medical Oncology and Urology, Duke Prostate and Urologic Cancer Center, Duke Cancer Institute Duke University, Durham.

Biostatistics (Lin) and Medical Affairs (Wong), Pfizer Inc, San Francisco.

出版信息

Ann Oncol. 2018 Nov 1;29(11):2200-2207. doi: 10.1093/annonc/mdy406.

DOI:10.1093/annonc/mdy406
PMID:30202945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6888025/
Abstract

BACKGROUND

Prognostic models are needed that reflect contemporary practice for men with metastatic castration-resistant prostate cancer (mCRPC). We sought to identify predictive and prognostic variables for overall survival (OS) in chemotherapy-naïve men with mCRPC treated with enzalutamide.

PATIENTS AND METHODS

Patients from the PREVAIL trial database (enzalutamide versus placebo) were randomly split 2 : 1 into training (n = 1159) and testing (n = 550) sets. Using the training set, 23 predefined variables were analyzed and a multivariable model predicting OS was developed and validated in an independent testing set.

RESULTS

Patient characteristics and outcomes were well balanced between training and testing sets; median OS was 32.7 months in each. The final validated multivariable model included 11 independent prognostic variables. Median OS for low-, intermediate-, and high-risk groups (testing set) defined by prognostic risk tertiles were not yet reached (NYR) (95% CI NYR-NYR), 34.2 months (31.5-NYR), and 21.1 months (17.5-25.0), respectively. Hazard ratios (95% CI) for OS in the low- and intermediate-risk groups versus high-risk group were 0.20 (0.14-0.29) and 0.40 (0.30-0.53), respectively. Secondary outcomes of response and progression differed widely in model-defined risk groups. Enzalutamide improved outcomes in all prognostic risk groups.

CONCLUSIONS

Our validated prognostic model incorporates variables routinely collected in chemotherapy-naïve men with mCRPC treated with enzalutamide, identifying subsets of patients with widely differing survival outcomes that provide useful information for external validation, patient care, and clinical trial design.

TRIAL REGISTRATION

ClinicalTrials.gov: NCT01212991.

摘要

背景

需要有反映转移性去势抵抗性前列腺癌(mCRPC)患者当代治疗实践的预后模型。我们旨在确定接受恩扎卢胺治疗的化疗初治 mCRPC 男性患者的总生存期(OS)的预测和预后变量。

患者和方法

来自 PREVAIL 试验数据库(恩扎卢胺对比安慰剂)的患者被随机分为 2:1 的训练(n=1159)和测试(n=550)组。使用训练集,分析了 23 个预先定义的变量,并在独立的测试集中开发和验证了预测 OS 的多变量模型。

结果

训练组和测试组之间患者特征和结局均衡;中位 OS 分别为 32.7 个月。最终验证的多变量模型包含 11 个独立的预后变量。通过预后风险三分位数定义的低、中、高危组(测试集)的中位 OS 尚未达到(NYR)(95%CI NYR-NYR),分别为 34.2 个月(31.5-NYR)、21.1 个月(17.5-25.0)。低危和中危组与高危组的 OS 风险比(95%CI)分别为 0.20(0.14-0.29)和 0.40(0.30-0.53)。模型定义的风险组中,反应和进展的次要结局差异很大。恩扎卢胺改善了所有预后风险组的结局。

结论

我们验证的预后模型纳入了化疗初治 mCRPC 患者接受恩扎卢胺治疗时常规收集的变量,确定了具有广泛不同生存结局的患者亚组,为外部验证、患者护理和临床试验设计提供了有用的信息。

试验注册

ClinicalTrials.gov:NCT01212991。