Clinical Utility of Circulating Tumour Cell Androgen Receptor Splice Variant-7 Status in Metastatic Castration-resistant Prostate Cancer
- PMID: 31036442
- DOI: 10.1016/j.eururo.2019.04.006
Clinical Utility of Circulating Tumour Cell Androgen Receptor Splice Variant-7 Status in Metastatic Castration-resistant Prostate Cancer
Abstract
Background: Detection of androgen receptor splice variant-7 (AR-V7) mRNA in circulating tumour cells (CTCs) is associated with worse outcome in metastatic castration-resistant prostate cancer (mCRPC). However, studies rarely report comparisons with CTC counts and biopsy AR-V7 protein expression.
Objective: To determine the reproducibility of AdnaTest CTC AR-V7 testing, and associations with clinical characteristics, CellSearch CTC counts, tumour biopsy AR-V7 protein expression and overall survival (OS).
Design, setting, and participants: CTC AR-V7 status was determined for 227 peripheral blood samples, from 181 mCRPC patients with CTC counts (202 samples; 136 patients) and matched mCRPC biopsies (65 samples; 58 patients).
Outcome measurements and statistical analysis: CTC AR-V7 status was associated with clinical characteristics, CTC counts, and tissue biopsy AR-V7 protein expression. The association of CTC AR-V7 status and other baseline variables with OS was determined.
Results and limitations: Of the samples, 35% were CTC+/AR-V7+. CTC+/AR-V7+ samples had higher CellSearch CTC counts (median CTC; interquartile range [IQR]: 60, 19-184 vs 9, 2-64; Mann-Whitney test p<0.001) and biopsy AR-V7 protein expression (median H-score, IQR: 100, 63-148 vs 15, 0-113; Mann-Whitney test p=0.004) than CTC+/AR-V7- samples. However, both CTC- (63%) and CTC+/AR-V7- (62%) patients had detectable AR-V7 protein in contemporaneous biopsies. After accounting for baseline characteristics, there was shorter OS in CTC+/AR-V7+ patients than in CTC- patients (hazard ratio [HR] 2.13; 95% confidence interval [CI] 1.23-3.71; p=0.02); surprisingly, there was no evidence that CTC+/AR-V7+ patients had worse OS than CTC+/AR-V7- patients (HR 1.26; 95% CI 0.73-2.17; p=0.4). A limitation of this study was the heterogeneity of treatment received.
Conclusions: Studies reporting the prognostic relevance of CTC AR-V7 status must account for CTC counts. Discordant CTC AR-V7 results and AR-V7 protein expression in matched, same-patient biopsies are reported.
Patient summary: Liquid biopsies that determine circulating tumour cell androgen receptor splice variant-7 status have the potential to impact treatment decisions in metastatic castration-resistant prostate cancer patients. Robust clinical qualification of these assays is required before their routine use.
Keywords: Androgen receptor; Androgen receptor splice variant-7; Biomarker; Liquid biopsy; Metastatic castration-resistant prostate cancer; Prognostic.
Copyright © 2019 The Author(s). Published by Elsevier B.V. All rights reserved.
Comment in
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Circulating tumor cell-based or tissue biopsy-based AR-V7 detection: which provides the greatest clinical utility?Ann Transl Med. 2019 Dec;7(Suppl 8):S354. doi: 10.21037/atm.2019.09.92. Ann Transl Med. 2019. PMID: 32016072 Free PMC article. No abstract available.
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Current status of circulating tumor cell androgen receptor splice variant-7 in metastatic castration-resistant prostate cancer.Ann Transl Med. 2019 Dec;7(Suppl 8):S375. doi: 10.21037/atm.2019.12.137. Ann Transl Med. 2019. PMID: 32016093 Free PMC article. No abstract available.
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Considerations for AR-V7 testing in clinical routine practice.Ann Transl Med. 2019 Dec;7(Suppl 8):S378. doi: 10.21037/atm.2019.12.136. Ann Transl Med. 2019. PMID: 32016096 Free PMC article. No abstract available.
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