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.
Ann Oncol. 2018 Nov 1;29(11):2200-2207. doi: 10.1093/annonc/mdy406.
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 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.
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.
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.
ClinicalTrials.gov: NCT01212991.
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。
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。
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。
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。
ClinicalTrials.gov:NCT01212991。