Zhang Tian, Dhawan Mallika S, Healy Patrick, George Daniel J, Harrison Michael R, Oldan Jorge, Chin Bennett, Armstrong Andrew J
Duke Cancer Institute, Divisions of Medical Oncology and Urology, Departments of Medicine and Surgery, Duke University Medical Center, Durham, NC.
University of California - San Francisco, San Francisco, CA.
Clin Genitourin Cancer. 2015 Aug;13(4):392-399. doi: 10.1016/j.clgc.2015.01.004. Epub 2015 Jan 24.
Abiraterone acetate (AA) has demonstrated improved outcomes in men with metastatic castration-resistant prostate cancer (mCRPC). However, data are lacking on the effect of AA on subsequent efficacy of enzalutamide or docetaxel.
We included men with mCRPC who received AA and subsequent enzalutamide or docetaxel by August 12, 2013. Patients were separated into 3 groups: group A, treated with AA then enzalutamide before chemotherapy; group B, treated with AA then docetaxel; and group C, treated with AA and enzalutamide after chemotherapy. The primary objective was to describe the response and overall survival with subsequent therapy.
There were 28 evaluable patients who received enzalutamide after AA (9 in group A and 19 in group C) and 13 patients who received docetaxel after AA (group B). Group A patients had more visceral disease and higher baseline prostate-specific antigen (PSA) levels, and group C men had a higher level of pain and multiple poor prognostic features. Median progression-free survival was 3.6, 5.1, and 2.8 months, respectively, and median overall survival was 8.5, not reached, and 9.6 months, respectively. A ≥ 50% PSA decline was achieved in 11%, 63%, and 5% of group A, B, and C patients, respectively. Radiographic or clinical progression as best response was noted in 55.5%, 30.8%, and 68.4% in each respective group.
In this chart review of consecutive men with progressive mCRPC after AA, we found modest activity for enzalutamide and docetaxel, with clear cross-resistance for AA and enzalutamide. These data might inform the complex treatment decisions after AA treatment.
醋酸阿比特龙(AA)已证明可改善转移性去势抵抗性前列腺癌(mCRPC)男性患者的预后。然而,关于AA对恩杂鲁胺或多西他赛后续疗效的影响的数据尚缺。
我们纳入了在2013年8月12日前接受AA及后续恩杂鲁胺或多西他赛治疗的mCRPC男性患者。患者被分为3组:A组,先接受AA治疗,然后在化疗前接受恩杂鲁胺治疗;B组,先接受AA治疗,然后接受多西他赛治疗;C组,在化疗后接受AA和恩杂鲁胺治疗。主要目的是描述后续治疗的反应和总生存期。
有28例可评估患者在接受AA治疗后接受了恩杂鲁胺治疗(A组9例,C组19例),13例患者在接受AA治疗后接受了多西他赛治疗(B组)。A组患者内脏疾病更多,基线前列腺特异性抗原(PSA)水平更高,C组男性疼痛程度更高且有多种不良预后特征。无进展生存期的中位数分别为3.6个月、5.1个月和2.8个月,总生存期的中位数分别为8.5个月、未达到和9.6个月。A、B、C组患者中分别有11%、63%和5%的患者PSA下降≥50%。各相应组中分别有55.5%、30.8%和68.4%的患者出现影像学或临床进展作为最佳反应。
在本次对AA治疗后病情进展的连续性mCRPC男性患者的病历回顾中,我们发现恩杂鲁胺和多西他赛有一定活性,且AA和恩杂鲁胺之间存在明显的交叉耐药性。这些数据可能为AA治疗后的复杂治疗决策提供参考。