Department of Urology, Kobe University Graduate School of Medicine, 7-5-1, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Med Oncol. 2017 Aug 17;34(9):163. doi: 10.1007/s12032-017-1024-0.
The purpose of this study was to evaluate the efficacy of cabazitaxel for patients with metastatic castration-resistant prostate cancer (mCRPC) after sequential therapy with docetaxel (DTX) and single or dual regimens of novel androgen receptor-axis-targeted (ARAT) agents. We retrospectively reviewed 84 consecutive patients treated with cabazitaxel at Kobe University Hospital and related hospitals from September 2014 to September 2016. The association of each prognostic parameter with progression-free survival (PFS) was evaluated, including the sequence of therapy. Patients were divided according to their treatment after receiving cabazitaxel as follows: group 1 (after DTX and single regimen of novel ARAT agent) and group 2 (after DTX and dual novel ARAT agents). Median PFS for cabazitaxel treatment was 10.3 months (range 4.5-14.2 months). Prostate-specific antigen (PSA) response rates (≥30%) were 46.8 and 46.1% in group 1 and group 2, respectively [p = 0.96, hazard ratio (HR) 1.02, 95% confidence interval (CI) 0.57-1.80]. PSA response rates (≥50%) were 43.8 and 26.9% in patients of group 1 and group 2, respectively (p = 0.18, HR 1.54, 95% CI 0.78-3.04). Univariate analysis revealed that PFS for cabazitaxel treatment was significantly associated with baseline alkaline phosphatase, bone metastasis, and prior sequential therapy. Multivariate analysis revealed that bone metastasis and prior sequential therapy were independently associated with PFS. Prior sequential therapy with single regimen or dual regimens of novel ARAT agents was independently associated with PFS of patients with mCRPC treated with cabazitaxel. The effect of cabazitaxel after the administration of DTX and single novel ARAT agent was more sustained.
本研究旨在评估卡巴他赛治疗多西他赛(DTX)序贯治疗后转移性去势抵抗性前列腺癌(mCRPC)患者的疗效,以及新型雄激素受体轴靶向(ARAT)药物的单药或双药方案。我们回顾性分析了 2014 年 9 月至 2016 年 9 月期间在神户大学医院和相关医院接受卡巴他赛治疗的 84 例连续患者。评估了每个预后参数与无进展生存期(PFS)的关系,包括治疗顺序。根据患者接受卡巴他赛治疗后的治疗方法将其分为两组:组 1(接受 DTX 和新型 ARAT 药物单药治疗)和组 2(接受 DTX 和新型 ARAT 药物双药治疗)。卡巴他赛治疗的中位 PFS 为 10.3 个月(范围 4.5-14.2 个月)。组 1 和组 2 的 PSA 缓解率(≥30%)分别为 46.8%和 46.1%[p=0.96,风险比(HR)1.02,95%置信区间(CI)0.57-1.80]。PSA 缓解率(≥50%)分别为 43.8%和 26.9%(p=0.18,HR 1.54,95% CI 0.78-3.04)。单因素分析显示,卡巴他赛治疗的 PFS 与基线碱性磷酸酶、骨转移和序贯治疗显著相关。多因素分析显示,骨转移和序贯治疗与 PFS 独立相关。新型 ARAT 药物单药或双药方案序贯治疗与 mCRPC 患者接受卡巴他赛治疗的 PFS 独立相关。DTX 和新型 ARAT 药物单药序贯治疗后卡巴他赛的疗效更持久。