From the Departments of Oncology (E.S.A., H.W., B.L., J.T.I., R.N., C.J.P., S.R.D., M.A.C., M.A.E.), Pathology (H.L.F., T.L.L., Q.Z., A.M.D.M.), and Urology (C.L., M.N., J.C.R., Yan Chen, W.B.I., J.L.), Johns Hopkins University School of Medicine, Baltimore; and Greehey Children's Cancer Research Institute (T.A.M., Yidong Chen) and the Department of Epidemiology and Biostatistics (Yidong Chen), University of Texas Health Science Center at San Antonio, San Antonio.
N Engl J Med. 2014 Sep 11;371(11):1028-38. doi: 10.1056/NEJMoa1315815. Epub 2014 Sep 3.
The androgen-receptor isoform encoded by splice variant 7 lacks the ligand-binding domain, which is the target of enzalutamide and abiraterone, but remains constitutively active as a transcription factor. We hypothesized that detection of androgen-receptor splice variant 7 messenger RNA (AR-V7) in circulating tumor cells from men with advanced prostate cancer would be associated with resistance to enzalutamide and abiraterone.
We used a quantitative reverse-transcriptase-polymerase-chain-reaction assay to evaluate AR-V7 in circulating tumor cells from prospectively enrolled patients with metastatic castration-resistant prostate cancer who were initiating treatment with either enzalutamide or abiraterone. We examined associations between AR-V7 status (positive vs. negative) and prostate-specific antigen (PSA) response rates (the primary end point), freedom from PSA progression (PSA progression-free survival), clinical or radiographic progression-free survival, and overall survival.
A total of 31 enzalutamide-treated patients and 31 abiraterone-treated patients were enrolled, of whom 39% and 19%, respectively, had detectable AR-V7 in circulating tumor cells. Among men receiving enzalutamide, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 53%, P=0.004) and shorter PSA progression-free survival (median, 1.4 months vs. 6.0 months; P<0.001), clinical or radiographic progression-free survival (median, 2.1 months vs. 6.1 months; P<0.001), and overall survival (median, 5.5 months vs. not reached; P=0.002). Similarly, among men receiving abiraterone, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 68%, P=0.004) and shorter PSA progression-free survival (median, 1.3 months vs. not reached; P<0.001), clinical or radiographic progression-free survival (median, 2.3 months vs. not reached; P<0.001), and overall survival (median, 10.6 months vs. not reached, P=0.006). The association between AR-V7 detection and therapeutic resistance was maintained after adjustment for expression of full-length androgen receptor messenger RNA.
Detection of AR-V7 in circulating tumor cells from patients with castration-resistant prostate cancer may be associated with resistance to enzalutamide and abiraterone. These findings require large-scale prospective validation. (Funded by the Prostate Cancer Foundation and others.).
剪接变异体 7 编码的雄激素受体同工型缺乏配体结合域,这是恩扎鲁胺和阿比特龙的靶点,但作为转录因子仍然持续激活。我们假设,在接受恩扎鲁胺或阿比特龙治疗的转移性去势抵抗性前列腺癌患者的循环肿瘤细胞中检测到雄激素受体剪接变异体 7 信使 RNA(AR-V7),与对恩扎鲁胺和阿比特龙的耐药性有关。
我们使用定量逆转录-聚合酶链反应检测来评估前瞻性纳入的转移性去势抵抗性前列腺癌患者循环肿瘤细胞中的 AR-V7,这些患者正在接受恩扎鲁胺或阿比特龙治疗。我们检查了 AR-V7 状态(阳性与阴性)与前列腺特异性抗原(PSA)反应率(主要终点)、无 PSA 进展(PSA 无进展生存期)、临床或影像学无进展生存期和总生存期之间的关联。
共纳入 31 名接受恩扎鲁胺治疗的患者和 31 名接受阿比特龙治疗的患者,其中分别有 39%和 19%的患者循环肿瘤细胞中可检测到 AR-V7。在接受恩扎鲁胺治疗的男性中,AR-V7 阳性患者的 PSA 反应率低于 AR-V7 阴性患者(0%比 53%,P=0.004),PSA 无进展生存期(中位数,1.4 个月比 6.0 个月;P<0.001)、临床或影像学无进展生存期(中位数,2.1 个月比 6.1 个月;P<0.001)和总生存期(中位数,5.5 个月比未达到;P=0.002)更短。同样,在接受阿比特龙治疗的男性中,AR-V7 阳性患者的 PSA 反应率低于 AR-V7 阴性患者(0%比 68%,P=0.004),PSA 无进展生存期(中位数,1.3 个月比未达到;P<0.001)、临床或影像学无进展生存期(中位数,2.3 个月比未达到;P<0.001)和总生存期(中位数,10.6 个月比未达到,P=0.006)更短。在调整全长雄激素受体信使 RNA 的表达后,AR-V7 检测与治疗耐药性之间的关联仍然存在。
在去势抵抗性前列腺癌患者的循环肿瘤细胞中检测到 AR-V7 可能与恩扎鲁胺和阿比特龙的耐药性有关。这些发现需要大规模的前瞻性验证。(由前列腺癌基金会等资助)。