4.6 Article

Clinical Utility of Circulating Tumour Cell Androgen Receptor Splice Variant-7 Status in Metastatic Castration-resistant Prostate Cancer

Journal

EUROPEAN UROLOGY
Volume 76, Issue 5, Pages 676-685

Publisher

ELSEVIER
DOI: 10.1016/j.eururo.2019.04.006

Keywords

Androgen receptor; Androgen receptor splice variant-7; Liquid biopsy; Biomarker; Prognostic; Metastatic castration-resistant prostate cancer

Funding

  1. Department of Defense Prostate Cancer Research Program [W81XWH-14-2-0183, W81XWH-12-PCRP-TIA, W81XWH13-2-0070]
  2. Pacific Northwest Prostate Cancer SPORE [P50CA97186]
  3. Institute for Prostate Cancer Research (IPCR), Veterans Affairs Research Program
  4. NIH/National Cancer Institute [P01CA163227]
  5. Prostate Cancer Foundation [20131017, 20131017-1]
  6. Patrick C. Walsh Prostate Cancer Research Fund
  7. NIH [R01 CA185297]
  8. US Department of Defense Prostate Cancer Research Program [W81XWH-15-2-0050]
  9. Movember Foundation/Prostate Cancer UK [CEO13-2-002]
  10. US Department of Defense [W81XWH-13-2-0093]
  11. Stand Up To Cancer [SU2C-AACR-DT0712]
  12. Cancer Research UK [CRM108X-A25144]
  13. UK Department of Health through an Experimental Cancer Medicine Centre [ECMC-CRM064X]
  14. Medical Research Council [MR/M018618/1]
  15. Academy of Medical Sciences/Prostate Cancer UK [SGCL15]
  16. Prostate Cancer Foundation Young Investigator Award
  17. MRC [MR/M018318/1] Funding Source: UKRI

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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. (C) 2019 The Author(s). Published by Elsevier B.V.

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