Department of Urology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Institute of Clinical Chemistry and Pathobiochemistry, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany; German Cancer Consortium, partner site Munich, Germany; German Cancer Research Center, Heidelberg, Germany.
Eur Urol. 2017 Nov;72(5):828-834. doi: 10.1016/j.eururo.2017.07.024. Epub 2017 Aug 14.
It has been demonstrated that androgen receptor splice variant 7 (AR-V7) expression in circulating tumor cells (CTCs) predicts poor treatment response in metastatic castration-resistant prostate cancer (mCRPC) patients treated with abiraterone or enzalutamide.
To develop a practical and robust liquid profiling approach for direct quantification of AR-V7 in peripheral whole blood without the need for CTC capture and to determine its potential for predicting treatment response in mCRPC patients.
DESIGN, SETTING, AND PARTICIPANTS: Whole blood samples from a prospective biorepository of 85 mCRPC patients before treatment initiation with abiraterone (n=56) or enzalutamide (n=29) were analyzed via droplet digital polymerase chain reaction.
The association of AR-V7 status with prostate-specific antigen (PSA) response defined by PSA decline ≥50% and with PSA-progression-free survival (PSA-PFS), clinical PFS, and overall survival (OS) was assessed.
High AR-V7 expression levels in whole blood were detectable in 18% (15/85) of patients. No patient with high AR-V7 expression achieved a PSA response, and AR-V7 status was an independent predictor of PSA response in multivariable logistic regression analysis (p=0.03). High AR-V7 expression was associated with shorter PSA-PFS (median 2.4 vs 3.7 mo; p<0.001), shorter clinical PFS (median 2.7 vs 5.5 mo; p<0.001), and shorter OS (median 4.0 vs. 13.9 mo; p<0.001). On multivariable Cox regression analysis, high AR-V7 expression remained an independent predictor of shorter PSA-PFS (hazard ratio [HR] 7.0, 95% confidence interval [CI] 2.3-20.7; p<0.001), shorter clinical PFS (HR 2.3, 95% CI 1.1-4.9; p=0.02), and shorter OS (HR 3.0, 95% CI 1.4-6.3; p=0.005).
Testing of AR-V7 mRNA levels in whole blood is a simple and promising approach to predict poor treatment outcome in mCRPC patients receiving abiraterone or enzalutamide.
We established a method for determining AR-V7 status in whole blood. This test predicted treatment resistance in patients with metastatic castration-resistant prostate cancer undergoing treatment with abiraterone or enzalutamide. Prospective validation is needed before application to clinical practice.
已有研究表明,雄激素受体剪接变异体 7(AR-V7)在循环肿瘤细胞(CTC)中的表达可预测接受阿比特龙或恩扎鲁胺治疗的转移性去势抵抗性前列腺癌(mCRPC)患者的治疗反应不佳。
开发一种实用且稳健的液体分析方法,可直接定量检测外周全血中的 AR-V7,无需捕获 CTC,并确定其在 mCRPC 患者中预测治疗反应的潜力。
设计、设置和参与者:在开始接受阿比特龙(n=56)或恩扎鲁胺(n=29)治疗前,前瞻性生物库中 85 例 mCRPC 患者的全血样本通过液滴数字聚合酶链反应进行分析。
评估 AR-V7 状态与前列腺特异性抗原(PSA)应答的关系,PSA 应答定义为 PSA 下降≥50%,以及与 PSA-无进展生存期(PSA-PFS)、临床无进展生存期(clinical PFS)和总生存期(OS)的关系。
在 85 例患者中,有 18%(15/85)的患者可检测到高 AR-V7 表达水平。没有高 AR-V7 表达的患者达到 PSA 应答,AR-V7 状态是多变量逻辑回归分析中 PSA 应答的独立预测因素(p=0.03)。高 AR-V7 表达与 PSA-PFS 更短(中位数 2.4 与 3.7 个月;p<0.001)、临床 PFS 更短(中位数 2.7 与 5.5 个月;p<0.001)和 OS 更短(中位数 4.0 与 13.9 个月;p<0.001)相关。在多变量 Cox 回归分析中,高 AR-V7 表达仍然是 PSA-PFS 更短的独立预测因素(风险比[HR]7.0,95%置信区间[CI]2.3-20.7;p<0.001)、临床 PFS 更短(HR 2.3,95% CI 1.1-4.9;p=0.02)和 OS 更短(HR 3.0,95% CI 1.4-6.3;p=0.005)。
检测全血中的 AR-V7 mRNA 水平是一种简单且有前途的方法,可预测接受阿比特龙或恩扎鲁胺治疗的 mCRPC 患者的治疗结局不佳。
我们建立了一种在全血中确定 AR-V7 状态的方法。该检测可预测接受阿比特龙或恩扎鲁胺治疗的转移性去势抵抗性前列腺癌患者的治疗耐药性。在应用于临床实践之前需要进行前瞻性验证。