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雄激素受体变异驱动的前列腺癌 II:临床研究进展。

Androgen receptor variant-driven prostate cancer II: advances in clinical investigation.

机构信息

Departments of Medicine, Surgery, and Pharmacology and Cancer Biology, Divisions of Medical Oncology and Urology, Duke Cancer Institute Center for Prostate and Urologic Cancers, Duke University, Durham, NC, USA.

Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Prostate Cancer Prostatic Dis. 2020 Sep;23(3):367-380. doi: 10.1038/s41391-020-0215-5. Epub 2020 Feb 24.

Abstract

BACKGROUND

Approximately 10-30% of men with mCRPC will test positive for AR-V7 using one of two analytically and clinically validated circulating tumor cell (CTC)-based assays. These men have poor outcomes with approved AR-targeting therapies but may retain sensitivity to chemotherapy. Here, we discuss the clinical implications of testing and strategies that may benefit AR splice variant (AR-V)-positive men and discuss whether such variants are passengers or drivers of aggressive clinical behavior.

METHODS

We conducted a systemic review of the literature, covering updates since our 2016 review on androgen receptor variants in mCRPC, outcomes, and existing and novel approaches to therapy. We provide an expert opinion about management strategies for AR-V7-positive men and key unanswered research questions.

RESULTS

AR-V7-positive men, defined by Epic nuclear protein detection or the modified AdnaTest mRNA detection in CTCs, identify a subset of men with mCRPC that have a low probability of response to AR-targeting therapy with short progression-free and overall survival in multivariable analyses. AR-variants do not exist in isolation, but rather in the context of a complex, heterogeneous, and evolving mCRPC genome and phenotype as well as patient-specific clinical heterogeneity, and multiple mechanisms of resistance likely exist in patients regardless of AR-V7 detection. Efforts to develop broader resistance assays are needed, and effective treatment strategies beyond taxanes are needed to address the causal driver role of AR-variants and to benefit patients with AR-V-expressing prostate cancer.

CONCLUSIONS

CTC AR-V7 detection using the AdnaTest mRNA or Epic nuclear protein assays represents the first analytically and prospective clinically validated liquid biopsy assays that may inform treatment decisions in men with mCRPC, particularly after failure of first-line AR-therapy. The importance of AR-variants is likely to increase with the earlier use of AR-targeting strategies in other settings, and novel interventions for these men are needed.

摘要

背景

约 10-30%的 mCRPC 男性患者使用两种经过分析和临床验证的基于循环肿瘤细胞(CTC)的检测方法中的一种,可检测到 AR-V7 呈阳性。这些男性使用已批准的 AR 靶向治疗的效果较差,但可能对化疗仍有敏感性。在这里,我们讨论了检测的临床意义以及可能使 AR 剪接变体(AR-V)阳性男性受益的策略,并讨论了这些变体是否是侵袭性临床行为的乘客或驱动因素。

方法

我们对文献进行了系统回顾,涵盖了自我们 2016 年关于 mCRPC 中雄激素受体变体的综述以来的最新更新、结局以及现有的和新的治疗方法。我们提供了有关 AR-V7 阳性男性管理策略的专家意见以及关键的未解决的研究问题。

结果

通过 Epic 核蛋白检测或 CTC 中改良的 AdnaTest mRNA 检测定义的 AR-V7 阳性男性,确定了 mCRPC 中一部分对 AR 靶向治疗反应可能性较低的男性,多变量分析显示其无进展生存期和总生存期较短。AR 变体并非孤立存在,而是存在于复杂、异质和不断演变的 mCRPC 基因组和表型以及患者特异性临床异质性中,并且无论是否检测到 AR-V7,患者中可能存在多种耐药机制。需要努力开发更广泛的耐药性检测方法,并且需要除紫杉烷以外的有效治疗策略来解决 AR 变体的因果驱动作用,并使表达 AR-V 的前列腺癌患者受益。

结论

使用 AdnaTest mRNA 或 Epic 核蛋白检测方法检测 CTC AR-V7 代表了第一种经过分析和前瞻性临床验证的液体活检检测方法,可能为 mCRPC 男性的治疗决策提供信息,特别是在一线 AR 治疗失败后。随着 AR 靶向策略在其他情况下的更早使用,AR 变体的重要性可能会增加,并且需要为这些男性提供新的干预措施。

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