Lu David, Krupa Rachel, Harvey Melissa, Graf Ryon P, Schreiber Nicole, Barnett Ethan, Carbone Emily, Jendrisak Adam, Gill Audrey, Orr Sarah, Scher Howard I, Schonhoft Joseph D
Epic Sciences, San Diego, California - USA.
Exact Sciences, Madison, Wisconsin - USA.
J Circ Biomark. 2020 Oct 23;9:13-19. doi: 10.33393/jcb.2020.2163. eCollection 2020 Jan-Dec.
Here we describe the development of a protein immunofluorescent assay for the detection of nuclear-localized androgen receptor variant 7 (AR-V7) protein within circulating tumor cells (CTCs) identified in patient blood samples. Used in the clinic, the test result serves as a validated biomarker of futility for patients with progressing metastatic castration-resistant prostate cancer (mCRPC) who are treated with androgen receptor targeted therapies (AATT) in whom nuclear-localized AR-V7 CTCs are identified and have received level 2A evidence in the 2019 National Cancer Center Network (NCCN) guidelines (v1.0).
Assay development was completed on the Epic Sciences rare cell detection platform using control cell lines of known AR-V7 status and clinical testing of mCRPC patient samples obtained at the decision point in management.
Using these samples, all assay parameters, scoring criteria, and clinical cutoffs for positivity were prospectively selected and locked. After assay lock, blinded clinical validation testing was initiated on multiple, independent, clinical cohorts as reported by Scher et al (JAMA Oncol. 2016;2:1441-1449; JAMA Oncol. 2018;4:1179-1186) and Armstrong et al (J Clin Oncol. 2019;37:1120-1129).
在此,我们描述了一种蛋白质免疫荧光检测方法的开发,用于检测在患者血液样本中鉴定出的循环肿瘤细胞(CTC)内的核定位雄激素受体变体7(AR-V7)蛋白。在临床应用中,该检测结果可作为一种经过验证的生物标志物,用于判定接受雄激素受体靶向治疗(AATT)的转移性去势抵抗性前列腺癌(mCRPC)进展患者治疗无效,在这些患者中已鉴定出核定位AR-V7 CTC,且该检测结果在2019年美国国立综合癌症网络(NCCN)指南(v1.0)中获得了2A类证据。
在Epic Sciences稀有细胞检测平台上完成检测方法的开发,使用已知AR-V7状态的对照细胞系,并对在管理决策点获得的mCRPC患者样本进行临床检测。
使用这些样本,前瞻性地选择并锁定了所有检测参数、评分标准和阳性临床临界值。在检测方法锁定后,如Scher等人(《美国医学会肿瘤学杂志》。2016年;2:1441 - 1449;《美国医学会肿瘤学杂志》。2018年;4:1179 - 1186)和Armstrong等人(《临床肿瘤学杂志》。2019年;37:1120 - 1129)所报道的,在多个独立临床队列上启动了盲法临床验证检测。