Department of Urology, Nara Medical University, Kashihara, Japan.
Department of Urology, Osaka International Cancer Institute, Osaka, Japan.
Int J Urol. 2019 Aug;26(8):797-803. doi: 10.1111/iju.14009. Epub 2019 May 5.
To report long-term outcome survival analysis of docetaxel-based chemotherapy combined with dexamethasone in castration-resistant prostate cancer patients (Japan-Multinational Trial Organization Pca10-01 trial).
The Japan-Multinational Trial Organization Pca10-01 phase II trial was a multicenter, prospective single-arm, phase II trial both in non-metastatic and metastatic castration-resistant prostate cancer patients that was organized by The Japan-Multinational Trial Organization. Patients received 75 mg/m of docetaxel (every 21 days) and 0.5 mg of dexamethasone orally twice a day continuing throughout the treatment period. The primary end-point of this additional analysis was overall survival. Secondary end-points were progression-free survival and safety.
Between January 2011 and February 2014, a total of 76 chemotherapy-naïve castration-resistant prostate cancer patients were enrolled. The median overall survival time was 42.5 months. The median overall survival time of M1 patients was 40.5 months (M0: not reached). The median progression-free survival time was 13.2 months (M0: 15.7 months and M1: 12.3 months). The multivariate analysis predicting overall survival of M1 patients showed that time to castration-resistant prostate cancer (≥20 months) was an independent parameter (hazard ratio 0.39, P = 0.023). Regarding the safety analysis, 36 out of 74 patients (48.6%) suffered from any grade of adverse events after the protocol treatment, and 18 patients (24.3%) had grade ≥3 adverse events.
Docetaxel-based chemotherapy combined with dexamethasone can achieve excellent survival efficacy not only in M0 castration-resistant prostate cancer patients, but also in M1 castration-resistant prostate cancer patients.
报告多西他赛联合地塞米松化疗在去势抵抗性前列腺癌患者中的长期生存分析(日本多国试验组织前列腺癌 10-01 试验)。
日本多国试验组织前列腺癌 10-01 期 2 期试验是一项多中心、前瞻性、单臂、2 期试验,由日本多国试验组织组织,纳入非转移性和转移性去势抵抗性前列腺癌患者。患者接受 75mg/m 的多西他赛(每 21 天一次)和地塞米松 0.5mg 口服,每天两次,持续整个治疗期间。本次额外分析的主要终点是总生存。次要终点为无进展生存和安全性。
2011 年 1 月至 2014 年 2 月期间,共纳入 76 例化疗初治的去势抵抗性前列腺癌患者。中位总生存时间为 42.5 个月。M1 患者的中位总生存时间为 40.5 个月(M0:未达到)。中位无进展生存时间为 13.2 个月(M0:15.7 个月,M1:12.3 个月)。多变量分析预测 M1 患者的总生存情况显示,去势抵抗性前列腺癌时间(≥20 个月)是独立参数(风险比 0.39,P=0.023)。关于安全性分析,74 例患者中有 36 例(48.6%)在方案治疗后出现任何级别的不良事件,18 例(24.3%)发生≥3 级不良事件。
多西他赛联合地塞米松化疗不仅能在 M0 去势抵抗性前列腺癌患者中获得良好的生存疗效,而且能在 M1 去势抵抗性前列腺癌患者中获得良好的生存疗效。