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[AR-V7雄激素受体变体作为用于治疗去势抵抗性转移性前列腺癌的雄激素受体靶向药物反应的预测指标]

[AR-V7 Androgen Receptor Variant as a Predictor of Response to Androgen-receptor Targeting Agents Used to Treat Castration-refractory Metastatic Prostate Cancer].

作者信息

Büchler Tomáš, Bobek Vladimír, Kološtová Katarína

出版信息

Klin Onkol. 2017 Winter;31(1):9-14. doi: 10.14735/amko20189.

Abstract

BACKGROUND

Several systemic treatment options are currently available for patients with metastatic castration-refractory prostate cancer (mCRPC), including the androgen-receptor targeting agents (ARTA) enzalutamide and abiraterone, the taxanes docetaxel and cabazitaxel, and the radioisotope drug 223-radium dichloride. In some patients with mCRCP, alternative splicing of androgen receptor (AR) mRNA occurs, resulting in the formation of a truncated AR lacking the androgen-binding domain. These receptors activate downstream signalling pathways even without the ligand. Recent studies show that the presence of the AR-V7 (ARV - AR variants) splicing variant is associated with resistance to ARTA. Bec>ause the presence of AR-V7 does not affect the efficacy of other systemic therapies used in mCRCPs, particularly taxanes, AR-V7 is a candidate predictive biomarker for the individualisation of mCRCP treatment. Two types of assays based on mRNA or abnormal protein detection are used to detect AR-V7 in circulating tumour cells.

AIM

To describe the current status of AR-V7 testing in mCRPC and possible applications of this method for predicting outcomes of ARTA therapy.

CONCLUSION

The percentage of CTC AR-V7+ in ARTA-naive men is relatively low at baseline, but in patients pretreated with ARTA, the prevalence of AR-V7 increases to 19-34%. Given the relatively high expected prevalence, AR-V7 testing may be economically feasible in this population. The proportion of AR-V7+ patients responding to ARTA retreatment appears to be very low, at only 4.8%. AR-V7 testing could thus be useful if an ARTA switch is considered in a patient progressing onto an ARTA drug. Both protein-based tests and mRNA-based tests are currently undergoing clinical validation in prospective studies, with results expected within a year.Key words: prostate cancer - abiraterone - enzalutamide - alternative splicing - drug resistanceSubmitted: 30. 8. 2017Accepted: 5. 11. 2017 doc. MUDr. Tomáš Büchler, Ph.D. received honorary lectures and publications from Astellas and Janssen and a travel grant from Janssen. Supported by Ministry of Health, Czech Republic - conceptual development of research organization Thomayer Hospital - TN 0064190. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.

摘要

背景

目前,转移性去势抵抗性前列腺癌(mCRPC)患者有多种全身治疗选择,包括雄激素受体靶向药物(ARTA)恩杂鲁胺和阿比特龙、紫杉烷类药物多西他赛和卡巴他赛,以及放射性同位素药物二氯化镭223。在一些mCRCP患者中,雄激素受体(AR)mRNA发生可变剪接,导致形成一种缺乏雄激素结合域的截短型AR。这些受体即使在没有配体的情况下也能激活下游信号通路。最近的研究表明,AR-V7(AR变异体)剪接变异体的存在与对ARTA的耐药性有关。由于AR-V7的存在不影响用于mCRCP的其他全身治疗的疗效,特别是紫杉烷类药物,AR-V7是mCRCP治疗个体化的候选预测生物标志物。基于mRNA或异常蛋白检测的两种检测方法用于检测循环肿瘤细胞中的AR-V7。

目的

描述mCRPC中AR-V7检测的现状以及该方法在预测ARTA治疗结果方面的可能应用。

结论

在未接受过ARTA治疗的男性中,基线时循环肿瘤细胞AR-V7阳性的比例相对较低,但在接受过ARTA预处理的患者中,AR-V7的患病率增加到19%至34%。鉴于预期患病率相对较高,AR-V7检测在该人群中可能在经济上可行。对ARTA再治疗有反应的AR-V7阳性患者比例似乎非常低,仅为4.8%。因此,如果考虑在进展到ARTA药物的患者中进行ARTA转换,AR-V7检测可能会有用。基于蛋白质的检测和基于mRNA的检测目前都在进行前瞻性研究的临床验证,预计一年内会有结果。

关键词

前列腺癌 - 阿比特龙 - 恩杂鲁胺 - 可变剪接 - 耐药性

提交日期

2017年8月30日

接受日期

2017年11月5日

医学博士Tomáš Büchler博士接受了安斯泰来和杨森公司的荣誉讲座和出版物,并获得了杨森公司的旅行资助。由捷克共和国卫生部资助 - Thomayer医院研究组织的概念发展 - TN 0064190。编辑委员会声明该手稿符合ICMJE关于生物医学论文的建议。

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