Armstrong Andrew J, Luo Jun, Nanus David M, Giannakakou Paraskevi, Szmulewitz Russell Z, Danila Daniel C, Healy Patrick, Anand Monika, Berry William R, Zhang Tian, Harrison Michael R, Lu Changxue, Chen Yan, Galletti Giuseppe, Schonhoft Joseph D, Scher Howard I, Wenstrup Richard, Tagawa Scott T, Antonarakis Emmanuel S, George Daniel J, Halabi Susan
Duke Cancer Institute Center for Prostate and Urologic Cancers, Department of Medicine, Duke University, Durham, NC.
Department of Urology, Johns Hopkins University, Baltimore, MD.
JCO Precis Oncol. 2020 Oct 28;4. doi: 10.1200/PO.20.00200. eCollection 2020.
Androgen receptor splice variant 7 (AR-V7) detection in circulating tumor cells (CTCs) is associated with a low probability of response and short progression-free (PFS) and overall survival (OS) in men with metastatic castration-resistant prostate cancer (mCRPC) treated with enzalutamide or abiraterone. However, it is unclear whether such men benefit from taxane chemotherapy.
PROPHECY is a multicenter prospective blinded study of patients with poor-risk mCRPC starting abiraterone or enzalutamide and observed through subsequent progression and taxane chemotherapy. We assessed AR-V7 status using the Johns Hopkins modified AdnaTest CTC AR-V7 messenger RNA assay and the Epic Sciences CTC nuclear-localized AR-V7 protein assay before treatment. The primary objective was to validate the independent prognostic value of CTC AR-V7 status based on radiographic/clinical PFS. OS, confirmed prostate-specific antigen (PSA), and objective radiologic responses were secondary end points.
We enrolled 118 men with mCRPC treated with abiraterone or enzalutamide, 51 of whom received subsequent docetaxel or cabazitaxel. Pretreatment CTC AR-V7 status by the Johns Hopkins and Epic Sciences assays was independently associated with worse PFS (hazard ratio [HR], 1.7; 95% CI, 1.0 to 2.9 and HR, 2.1; 95% CI, 1.0 to 4.4, respectively) and OS (HR, 3.3; 95% CI, 1.7 to 6.3 and HR, 3.0; 95% CI, 1.4 to 6.3, respectively) and a low probability of confirmed PSA responses, ranging from 0% to 11%, during treatment with abiraterone or enzalutamide. At progression, subsequent CTC AR-V7 detection was not associated with an inferior PSA or radiographic response or worse PFS or OS with subsequent taxane chemotherapy after adjusting for CellSearch CTC enumeration and clinical prognostic factors.
Detection of AR-V7 in CTCs by two different blood-based assays is independently associated with shorter PFS and OS with abiraterone or enzalutamide, but such men with AR-V7-positive disease still experience clinical benefits from taxane chemotherapy.
在接受恩杂鲁胺或阿比特龙治疗的转移性去势抵抗性前列腺癌(mCRPC)男性患者中,循环肿瘤细胞(CTC)中的雄激素受体剪接变体7(AR-V7)检测与缓解概率低、无进展生存期(PFS)短和总生存期(OS)短相关。然而,尚不清楚这类男性患者是否能从紫杉烷类化疗中获益。
PROPHECY是一项多中心前瞻性盲法研究,研究对象为开始接受阿比特龙或恩杂鲁胺治疗的高危mCRPC患者,并对其后续进展和紫杉烷类化疗进行观察。我们在治疗前使用约翰霍普金斯大学改良的AdnaTest CTC AR-V7信使核糖核酸检测法和Epic Sciences CTC核定位AR-V7蛋白检测法评估AR-V7状态。主要目的是基于影像学/临床PFS验证CTC AR-V7状态的独立预后价值。OS、确诊的前列腺特异性抗原(PSA)和客观影像学缓解为次要终点。
我们纳入了118例接受阿比特龙或恩杂鲁胺治疗的mCRPC男性患者,其中51例随后接受了多西他赛或卡巴他赛治疗。通过约翰霍普金斯大学检测法和Epic Sciences检测法检测的治疗前CTC AR-V7状态分别与较差的PFS(风险比[HR],1.7;95%CI,1.0至2.9和HR,2.1;95%CI,1.0至4.4)和OS(HR,3.3;95%CI,1.7至6.3和HR,3.0;95%CI,1.4至6.3)以及在接受阿比特龙或恩杂鲁胺治疗期间确诊PSA缓解概率低(范围为0%至11%)独立相关。在疾病进展时,在对CellSearch CTC计数和临床预后因素进行校正后,后续CTC AR-V7检测与较差的PSA或影像学缓解、较差的PFS或OS以及后续紫杉烷类化疗无关。
通过两种不同的基于血液的检测方法检测CTC中的AR-V7与使用阿比特龙或恩杂鲁胺治疗时较短的PFS和OS独立相关,但这类AR-V7阳性疾病的男性患者仍能从紫杉烷类化疗中获得临床益处。