AR-V7 and Resistance to Enzalutamide and Abiraterone in Prostate Cancer
Johns Hopkins University · The University of Texas at San Antonio Health Science Center · +3 more institutions
Abstract
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.
Citation impact
- FWCI
- 216.43
- Percentile
- 100%
- References
- 34
Authors
21- ESEmmanuel S. AntonarakisCorresponding
Johns Hopkins University, The University of Texas at San Antonio Health Science Center, Johns Hopkins Medicine, Anna Needs Neuroblastoma Answers
- CLChangxue Lu
Johns Hopkins University, Johns Hopkins Medicine
- HWHao Wang
Johns Hopkins University, Johns Hopkins Medicine
- BLBrandon Luber
Johns Hopkins University, Johns Hopkins Medicine
- MNMari Nakazawa
Johns Hopkins University, Johns Hopkins Medicine
Topics & keywords
- Enzalutamide
- Medicine
- Prostate cancer
- Androgen receptor
- Internal medicine
- Oncology
- Progression-free survival
- Urology
- Good health and well-being