Ueda Yujiro, Matsubara Nobuaki, Takizawa Itsuhiro, Nishiyama Tsutomu, Tabata Ken-Ichi, Satoh Takefumi, Kamiya Naoto, Suzuki Hiroyoshi, Kawahara Takashi, Uemura Hiroji
Department of Breast and Medical Oncology, National Cancer Center Hospital East, Chiba.
Department of Breast and Medical Oncology, National Cancer Center Hospital East, Chiba
Jpn J Clin Oncol. 2015 Aug;45(8):774-9. doi: 10.1093/jjco/hyv070. Epub 2015 May 15.
Abiraterone acetate and docetaxel are promising treatment options for metastatic castration-resistant prostate cancer patients. However, the optimal sequencing of these agents is unclear, and no previous reports discuss Japanese metastatic castration-resistant prostate cancer patients. The purpose of this analysis is to reveal the outcomes of Japanese metastatic castration-resistant prostate cancer patients treated with abiraterone acetate followed by docetaxel.
We retrospectively reviewed Japanese Phase 1 and Phase 2 trials of metastatic castration-resistant prostate cancer patients treated with abiraterone acetate until disease progression and subsequently treated with docetaxel. The primary outcome measure was the rates of prostate-specific antigen declines ≧30 and ≧50%, respectively, with docetaxel. Secondary outcome measures included progression-free survival with docetaxel, and overall survival after initiation of abiraterone acetate and docetaxel. We performed correlation analysis between previous prostate-specific antigen response to abiraterone acetate and subsequent prostate-specific antigen response to docetaxel.
We identified 15 patients had experienced disease progression with abiraterone acetate and subsequently were treated with docetaxel. Prostate-specific antigen declines ≧30 and ≧50% with docetaxel were observed in five patients (33%) and two patients (13%), respectively. The median progression-free survival with docetaxel was 3.7 months (95% confidence interval: 2.9-4.6). The median overall survival from initiation of docetaxel and abiraterone acetate were 14.4 months (95% confidence interval: 6.3-22.4), and 25.7 months (95% confidence interval: 20.1-30.7), respectively. No significant correlation was observed between these prostate-specific antigen responses (Pearson r = 0.206, P = 0.46).
The efficacy of docetaxel in Japanese mCRPC patients that was resistant to abiraterone acetate was modest. The prostate-specific antigen response to previous abiraterone acetate could not predict the efficacy of subsequent docetaxel. Larger prospective trials are needed to validate these findings.
醋酸阿比特龙和多西他赛是转移性去势抵抗性前列腺癌患者很有前景的治疗选择。然而,这些药物的最佳用药顺序尚不清楚,且之前没有关于日本转移性去势抵抗性前列腺癌患者的报道。本分析的目的是揭示接受醋酸阿比特龙序贯多西他赛治疗的日本转移性去势抵抗性前列腺癌患者的治疗结果。
我们回顾性分析了日本针对转移性去势抵抗性前列腺癌患者开展的1期和2期试验,这些患者先接受醋酸阿比特龙治疗直至疾病进展,随后接受多西他赛治疗。主要结局指标分别是接受多西他赛治疗后前列腺特异性抗原下降≥30%和≥50%的比例。次要结局指标包括接受多西他赛治疗后的无进展生存期,以及开始使用醋酸阿比特龙和多西他赛治疗后的总生存期。我们对之前醋酸阿比特龙治疗时前列腺特异性抗原的反应与随后多西他赛治疗时前列腺特异性抗原的反应进行了相关性分析。
我们确定有15例患者在接受醋酸阿比特龙治疗后疾病进展,随后接受了多西他赛治疗。接受多西他赛治疗后,分别有5例患者(33%)和2例患者(13%)的前列腺特异性抗原下降≥30%和≥50%。接受多西他赛治疗的中位无进展生存期为3.7个月(95%置信区间:2.9 - 4.6)。从开始使用多西他赛和醋酸阿比特龙治疗后的中位总生存期分别为14.4个月(95%置信区间:6.3 - 22.4)和25.7个月(95%置信区间:20.1 - 30.7)。这些前列腺特异性抗原反应之间未观察到显著相关性(Pearson相关系数r = 0.206,P = 0.46)。
多西他赛对醋酸阿比特龙耐药的日本mCRPC患者的疗效一般。之前醋酸阿比特龙治疗时前列腺特异性抗原的反应无法预测随后多西他赛治疗的疗效。需要开展更大规模的前瞻性试验来验证这些发现。