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

被引:2397
作者
Antonarakis, Emmanuel S. [1 ]
Lu, Changxue [3 ]
Wang, Hao [1 ]
Luber, Brandon [1 ]
Nakazawa, Mary [3 ]
Roeser, Jeffrey C. [3 ]
Chen, Yan [3 ]
Mohammad, Tabrez A. [4 ]
Chen, Yidong [4 ,5 ]
Fedor, Helen L. [2 ]
Lotan, Tamara L. [2 ]
Zheng, Qizhi [2 ]
De Marzo, Angelo M. [2 ]
Isaacs, John T. [1 ]
Isaacs, William B. [3 ]
Nadal, Rosa [1 ]
Paller, Channing J. [1 ]
Denmeade, Samuel R. [1 ]
Carducci, Michael A. [1 ]
Eisenberger, Mario A. [1 ]
Luo, Jun [3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21287 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Greehey Childrens Canc Res Inst, San Antonio, TX 78229 USA
[5] Univ Texas Hlth Sci Ctr San Antonio, Dept Epidemiol & Biostat, San Antonio, TX 78229 USA
基金
美国国家卫生研究院;
关键词
RECEPTOR SPLICE VARIANTS; ACTIVE ANDROGEN RECEPTOR; INCREASED SURVIVAL; INHIBITOR; ACETATE; CHEMOTHERAPY; TUMORS;
D O I
10.1056/NEJMoa1315815
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
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.
引用
收藏
页码:1028 / 1038
页数:11
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