South Texas Accelerated Research Therapeutics (START), Center for Cancer Care, San Antonio, TX 78229, USA.
Cancer Chemother Pharmacol. 2012 Aug;70(2):305-13. doi: 10.1007/s00280-012-1916-9. Epub 2012 Jul 3.
Abiraterone is the active metabolite of the pro-drug abiraterone acetate (AA) and a selective inhibitor of CYP17, a key enzyme in testosterone synthesis, and improves overall survival in postdocetaxel metastatic castration-resistant prostate cancer (mCRPC). This open-label, single-arm phase 1b study was conducted to assess the effect of AA and abiraterone on the QT interval.
The study was conducted in 33 patients with mCRPC. Patients received AA 1,000 mg orally once daily + prednisone 5 mg orally twice daily. Electrocardiograms (ECGs) were collected in triplicate using 12-lead Holter monitoring. Baseline ECGs were obtained on Cycle 1 Day-1. Serial ECG recordings and time-matched pharmacokinetic (PK) blood samples were collected over 24 h on Cycle 1 Day 1 and Cycle 2 Day 1. Serial PK blood samples were also collected over 24 h on Cycle 1 Day 8.
After AA administration, the upper bound of the 2-sided 90 % confidence interval (CI) for the mean baseline-adjusted QTcF change was <10 ms; no patients discontinued due to QTc prolongation or adverse events. No apparent relationship between change in QTcF and abiraterone plasma concentrations was observed [estimated slope (90 % CI): 0.0031 (-0.0040, 0.0102)].
There is no significant effect of AA plus prednisone on the QT/QTc interval in patients with mCRPC.
阿比特龙是前药醋酸阿比特龙(AA)的活性代谢物,是睾酮合成关键酶 CYP17 的选择性抑制剂,可改善多西他赛化疗后转移性去势抵抗性前列腺癌(mCRPC)患者的总生存期。本开放标签、单臂 1b 期研究旨在评估 AA 和阿比特龙对 QT 间期的影响。
该研究纳入 33 例 mCRPC 患者。患者接受 AA 1000mg 口服,每日 1 次+泼尼松 5mg 口服,每日 2 次。使用 12 导联 Holter 监测器采集 3 份心电图(ECG)。第 1 周期第 1 天获取基线 ECG。第 1 周期第 1 天和第 2 周期第 1 天连续采集 24 小时的心电图记录和时间匹配的药代动力学(PK)血样。第 1 周期第 8 天还连续采集 24 小时的 PK 血样。
AA 给药后,平均基线校正后 QTcF 变化的双侧 90%置信区间(CI)上限<10ms;无患者因 QTc 延长或不良事件而停药。未观察到 QTcF 变化与阿比特龙血浆浓度之间存在明显关系[估计斜率(90%CI):0.0031(-0.0040,0.0102)]。
AA 加泼尼松对 mCRPC 患者的 QT/QTc 间期无显著影响。