Tsao Che-Kai, Sfakianos John, Liaw Bobby, Gimpel-Tetra Kiev, Kemeny Margaret, Bulone Linda, Shahin Mohammad, Oh William Kyu, Galsky Matthew David
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA
Department of Urology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Oncologist. 2016 Dec;21(12):1414-e9. doi: 10.1634/theoncologist.2016-0026. Epub 2016 Oct 14.
The safety and activity findings of abiraterone acetate plus prednisone treatment in black men with mCRPC were similar to results from previously conducted studies with largely white populations.Poor trial accrual continues to be a challenge in black men with mCRPC and further efforts are needed to address such underrepresentation.
Self-identified black men have higher incidence and mortality from prostate cancer in the United States compared with white men but are dramatically underrepresented in clinical trials exploring novel therapies for metastatic castration-resistant prostate cancer (mCRPC).
Black men with mCRPC were treated with abiraterone acetate (AA), 1,000 mg daily, and prednisone (P), 5 mg twice daily. The primary objective was to determine antitumor activity (defined by a ≥30% decline in prostate-specific antigen [PSA] level) and to correlate germline polymorphisms in androgen metabolism genes with antitumor activity. Secondary objectives included determining safety, post-treatment changes in measurable disease, and time to disease progression.
From April 2013 to March 2016, a total of 11 black men were enrolled and received AA plus P (AA+P); 7 of 10 evaluable patients were docetaxel naive. Post-treatment declines in PSA level of ≥30% were achieved in 90% of patients. The side effect profile was consistent with prior clinical trials exploring AA+P in mCRPC. Due to poor accrual, the study was closed prematurely with insufficient sample size for the planned pharmacogenetic analyses.
In this small prospective study terminated for poor accrual, the safety and activity of AA+P in black men with mCRPC was similar to that reported in prior studies exploring AA in largely white populations. Further efforts are needed to address underrepresentation of black men in mCRPC trials.
醋酸阿比特龙联合泼尼松治疗转移性去势抵抗性前列腺癌(mCRPC)黑人男性的安全性和活性研究结果,与之前主要针对白人人群进行的研究结果相似。在mCRPC黑人男性中,试验入组率低仍然是一个挑战,需要进一步努力解决这种代表性不足的问题。
在美国,自我认定的黑人男性前列腺癌的发病率和死亡率高于白人男性,但在探索转移性去势抵抗性前列腺癌(mCRPC)新疗法的临床试验中,他们的代表性极低。
mCRPC黑人男性患者接受醋酸阿比特龙(AA)治疗,每日1000毫克,泼尼松(P)治疗,每日两次,每次5毫克。主要目标是确定抗肿瘤活性(定义为前列腺特异性抗原[PSA]水平下降≥30%),并将雄激素代谢基因中的种系多态性与抗肿瘤活性相关联。次要目标包括确定安全性、可测量疾病的治疗后变化以及疾病进展时间。
2013年4月至2016年3月,共有11名黑人男性入组并接受AA加P(AA + P)治疗;10名可评估患者中有7名未接受过多西他赛治疗。90%的患者治疗后PSA水平下降≥30%。副作用情况与之前探索AA + P治疗mCRPC的临床试验一致。由于入组率低,该研究提前结束,样本量不足,无法进行计划中的药物遗传学分析。
在这项因入组率低而终止的小型前瞻性研究中,AA + P治疗mCRPC黑人男性的安全性和活性与之前在主要为白人人群中探索AA的研究报告相似。需要进一步努力解决mCRPC试验中黑人男性代表性不足的问题。