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CTC 衍生的 AR-V7 检测作为晚期前列腺癌的预后和预测生物标志物。

CTC-derived AR-V7 detection as a prognostic and predictive biomarker in advanced prostate cancer.

机构信息

a Department of Oncology , Hospital Sirio-Libanes , Sao Paulo , Brazil.

b Departments of Oncology and Urology, Sidney Kimmel Comprehensive Cancer Center , Johns Hopkins University School of Medicine , Baltimore , MA , USA.

出版信息

Expert Rev Mol Diagn. 2018 Feb;18(2):155-163. doi: 10.1080/14737159.2018.1427068. Epub 2018 Jan 16.

DOI:10.1080/14737159.2018.1427068
PMID:29319382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6088794/
Abstract

Prostate cancer is a highly heterogeneous disease, with remarkably different prognosis across all stages. Increased circulating tumor cell (CTC) count (≥ 5) using the CellSearch assay has been identified as one of the markers that can be used to predict survival, with added value beyond currently available prognostic factors. Recently, androgen receptor splice variant 7 (AR-V7) detection has been associated with worse outcomes for patients with castration-resistant prostate cancer (CRPC) treated with novel androgen receptor-signaling (ARS) inhibitors such as abiraterone and enzalutamide but not taxane chemotherapies. Areas covered: In this manuscript, the authors review the available biomarkers in CRPC and discuss emerging data on the value of CTC-derived AR-V7 status to assess prognosis and its potential role to guide treatment selection for patients with advanced prostate cancer. Expert commentary: Current evidence supports AR-V7 status as a prognostic biomarker and also as a potential predictive biomarker for patients with mCRPC. The authors expect that the incorporation of AR-V7 status and other biomarkers (e.g. AR mutations) in the sequential assessment of patients with advanced prostate cancer will lead to a more rational use of available and future therapies, with significant improvements in outcomes for our patients.

摘要

前列腺癌是一种高度异质性疾病,在所有阶段的预后差异显著。使用 CellSearch 检测方法检测到的循环肿瘤细胞 (CTC) 计数增加(≥5)已被确定为可用于预测生存的标志物之一,其价值超过了目前可用的预后因素。最近,雄激素受体剪接变体 7 (AR-V7) 的检测与接受新型雄激素受体信号 (ARS) 抑制剂(如阿比特龙和恩杂鲁胺)治疗的去势抵抗性前列腺癌 (CRPC) 患者的预后较差相关,但与紫杉烷化疗无关。

涵盖领域

在本文中,作者回顾了 CRPC 中可用的生物标志物,并讨论了关于 CTC 衍生的 AR-V7 状态评估预后的价值及其潜在作用,以指导晚期前列腺癌患者治疗选择的新兴数据。

专家评论

目前的证据支持 AR-V7 状态作为一种预后生物标志物,也可能作为 mCRPC 患者的潜在预测生物标志物。作者预计,在对晚期前列腺癌患者进行连续评估时,将 AR-V7 状态和其他生物标志物(如 AR 突变)纳入其中,将导致更合理地使用现有和未来的治疗方法,并显著改善我们患者的预后。

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JCO Precis Oncol. 2017;2017. doi: 10.1200/PO.17.00127. Epub 2017 Oct 30.
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Novel Junction-specific and Quantifiable In Situ Detection of AR-V7 and its Clinical Correlates in Metastatic Castration-resistant Prostate Cancer.新型接头特异性和可量化原位检测转移性去势抵抗性前列腺癌中的 AR-V7 及其临床相关性。
Eur Urol. 2018 May;73(5):727-735. doi: 10.1016/j.eururo.2017.08.009. Epub 2017 Sep 1.
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Phenotypic Heterogeneity of Circulating Tumor Cells Informs Clinical Decisions between AR Signaling Inhibitors and Taxanes in Metastatic Prostate Cancer.
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The Role of Circulating Tumor Cells as a Liquid Biopsy for Cancer: Advances, Biology, Technical Challenges, and Clinical Relevance.循环肿瘤细胞作为癌症液体活检的作用:进展、生物学特性、技术挑战及临床相关性
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