Petrioli Roberto, Roviello Giandomenico, Fiaschi Anna I, Laera Letizia, Bianco Vincenzo, Ponchietti Roberto, Barbanti Gabriele, Francini Edoardo
Medical Oncology Unit, Santa Maria alle Scotte Hospital, University of Siena, Italy.
Medical Oncology Unit, Santa Maria alle Scotte Hospital, University of Siena, Italy.
Clin Genitourin Cancer. 2015 Oct;13(5):441-6. doi: 10.1016/j.clgc.2015.03.004. Epub 2015 Mar 26.
The aim of this phase 2 study was to evaluate the activity and tolerability of low-dose estramustine phosphate (EMP) with concomitant low-dose acetylsalicylic acid (ASA) as a thromboprophylactic agent in heavily pretreated patients with advanced castration-resistant prostate cancer.
Patients received 420 mg of oral EMP twice daily and oral ASA 100 mg once daily. The primary endpoint was prostate-specific antigen response. All of the patients had been previously treated with docetaxel and abiraterone acetate, and 12 had also received cabazitaxel.
Thirty-one patients were enrolled. Prostate-specific antigen response was observed in 9 patients (29.0%; 95% confidence interval [CI], 14-48). Median progression-free survival was 3.6 months (95% CI, 2.2-5.6), and median overall survival was 7.6 months (95% CI, 6.9-9.7). Treatment was generally well tolerated, and no grade 3/4 toxicity was observed. Ten patients (32.2%) had grade 2 nausea and vomiting. No cardiovascular event and no major bleeding occurred. No venous thromboembolism event was observed.
Low-dose EMP with concomitant low-dose ASA seems to be a safe treatment option with some activity for patients with advanced castration-resistant prostate cancer who have been heavily pretreated.
本2期研究旨在评估低剂量磷酸雌莫司汀(EMP)联合低剂量乙酰水杨酸(ASA)作为血栓预防药物,在接受过大量治疗的晚期去势抵抗性前列腺癌患者中的活性和耐受性。
患者每日口服两次420 mg的EMP,每日口服一次100 mg的ASA。主要终点是前列腺特异性抗原反应。所有患者此前均接受过多西他赛和醋酸阿比特龙治疗,12例患者还接受过卡巴他赛治疗。
共纳入31例患者。9例患者(29.0%;95%置信区间[CI],14 - 48)观察到前列腺特异性抗原反应。中位无进展生存期为3.6个月(95% CI,2.2 - 5.6),中位总生存期为7.6个月(95% CI,6.9 - 9.7)。治疗总体耐受性良好,未观察到3/4级毒性。10例患者(32.2%)出现2级恶心和呕吐。未发生心血管事件和大出血。未观察到静脉血栓栓塞事件。
低剂量EMP联合低剂量ASA似乎是一种安全的治疗选择,对接受过大量治疗的晚期去势抵抗性前列腺癌患者有一定活性。