Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Hubei Institute of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Institute of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Eur Urol Focus. 2018 Jul;4(4):529-539. doi: 10.1016/j.euf.2017.01.004. Epub 2017 Jan 23.
Androgen receptor splice variant 7 (AR-V7) may be associated with resistance to next-generation androgen receptor signaling (ARS) inhibitors in castration-resistant prostate cancer (CRPC) sensitive to chemotherapy.
To evaluate the prognostic value of AR-V7 for prostate specific antigen (PSA) response, progression-free survival (PFS), and overall survival (OS) among CRPC patients treated with ARS inhibitors or chemotherapy.
A search of PubMed, Embase, and Web of Science databases was performed using the keywords "prostate cancer", "prostate tumor", "prostate neoplasm", "prostate carcinoma"; "AR-V7", "AR3", "androgen receptor splicing variant-7" and "androgen receptor-3". Fourteen trials published up to August 2016 were selected.
A significantly greater proportion of CRPCs than newly diagnosed prostate cancers were AR-V7-positive (odds ratio [OR] 8.29, 95% confidence interval [CI] 5.06-13.57; p<0.001). AR-V7-positive patients treated with ARS inhibitors had a significantly lower PSA response than those who were AR-V7-negative (OR 0.05, 95% CI 0.02-0.16; p<0.001).The difference was not significant in chemotherapy-treated patients (OR 0.64, 95% CI 0.3-1.33; p=0.23). Both PFS (hazard ratio [HR] 4.05, 95% CI 1.91-8.59; p=0.0003) and OS (HR 4.79, 95% CI 2.14-10.72; p<0.001) were better in AR-V7-negative than AR-V7-positive CRPC patients treated with ARS inhibitors. In chemotherapy patients, AR-V7 status had no significant effect on PFS (HR 1.26, 95% CI 0.80-2.00; p=0.32).However, AR-V7-negative patients had significantly better OS (HR 2.82, 95% CI 1.72-4.62; p<0.001). The limitations of our meta-analysis were differences in study sample size and design, AR-V7 assay, and disease characteristics.
AR-V7 positivity was associated with poorer PSA response and PFS prognosis in CRPC patients treated with ARS inhibitors, but did not affect outcomes except OS for those treated with chemotherapy. Additional studies are warranted to confirm these findings.
We concluded from several studies that androgen receptor splice variant 7 (AR-V7) could predict the outcomes of prostate cancer. AR-V7-positive patients have poorer outcomes when treated with abiraterone or enzalutamide, but relatively better outcomes when treated by chemotherapy.
雄激素受体剪接变异体 7(AR-V7)可能与化疗敏感的去势抵抗性前列腺癌(CRPC)对下一代雄激素受体信号转导(ARS)抑制剂的耐药性有关。
评估 AR-V7 对接受 ARS 抑制剂或化疗治疗的 CRPC 患者前列腺特异性抗原(PSA)反应、无进展生存期(PFS)和总生存期(OS)的预后价值。
使用“前列腺癌”、“前列腺肿瘤”、“前列腺癌”、“前列腺癌”等关键词,在 PubMed、Embase 和 Web of Science 数据库中进行了搜索。 “AR-V7”、“AR3”、“雄激素受体剪接变异体-7”和“雄激素受体-3”。 选择了截至 2016 年 8 月发表的 14 项试验。
与新诊断的前列腺癌相比,CRPC 中 AR-V7 阳性的比例明显更高(比值比 [OR] 8.29,95%置信区间 [CI] 5.06-13.57;p<0.001)。接受 ARS 抑制剂治疗的 AR-V7 阳性患者的 PSA 反应明显低于 AR-V7 阴性患者(OR 0.05,95%CI 0.02-0.16;p<0.001)。接受化疗的患者差异不显著(OR 0.64,95%CI 0.3-1.33;p=0.23)。 AR-V7 阴性患者的 PFS(风险比 [HR] 4.05,95%CI 1.91-8.59;p=0.0003)和 OS(HR 4.79,95%CI 2.14-10.72;p<0.001)均优于 AR-V7 阳性患者接受 ARS 抑制剂治疗的患者。在化疗患者中,AR-V7 状态对 PFS(HR 1.26,95%CI 0.80-2.00;p=0.32)无显著影响。然而,AR-V7 阴性患者的 OS 明显更好(HR 2.82,95%CI 1.72-4.62;p<0.001)。我们的荟萃分析存在局限性,包括研究样本量和设计、AR-V7 检测和疾病特征的差异。
AR-V7 阳性与接受 ARS 抑制剂治疗的 CRPC 患者 PSA 反应和 PFS 预后较差相关,但对接受化疗治疗的患者的预后(除 OS 外)无影响。需要进一步的研究来证实这些发现。
我们从几项研究中得出结论,雄激素受体剪接变体 7(AR-V7)可以预测前列腺癌的结果。 AR-V7 阳性患者接受阿比特龙或恩杂鲁胺治疗的结局较差,但接受化疗治疗的结局相对较好。