AR-V7 and Resistance to Enzalutamide and Abiraterone in Prostate Cancer

Emmanuel S. Antonarakis(Johns Hopkins University), Changxue Lu(Johns Hopkins University), Hao Wang(Johns Hopkins University), Brandon Luber(Johns Hopkins University), Mari Nakazawa(Johns Hopkins University), Jeffrey C. Roeser(Johns Hopkins University), Yan Chen(Johns Hopkins University), Tabrez A. Mohammad(The University of Texas at San Antonio Health Science Center), Yidong Chen(Cancer Research And Biostatistics), Helen Fedor(Johns Hopkins University), Tamara L. Lotan(Johns Hopkins University), Qizhi Zheng(Johns Hopkins University), Angelo M. De Marzo(Johns Hopkins University), John T. Isaacs(Johns Hopkins University), William B. Isaacs(Johns Hopkins University), Rosa Nadal(Johns Hopkins University), Channing J. Paller(Johns Hopkins University), Samuel R. Denmeade(Johns Hopkins University), Michael A. Carducci(Johns Hopkins University), Mario A. Eisenberger(Johns Hopkins University), Jun Luo(Johns Hopkins University)
New England Journal of Medicine
September 3, 2014
Cited by 2,676Open Access
Full Text

Abstract

BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.).


Related Papers

No related papers found

Powered by citation graph analysis