Cell-Free DNA Alterations in the AR Enhancer and Locus Predict Resistance to AR-Directed Therapy in Patients With Metastatic Prostate Cancer

Author:

Dang Ha X.123,Chauhan Pradeep S.4,Ellis Haley14,Feng Wenjia4,Harris Peter K.4,Smith Grace4,Qiao Mark4,Dienstbach Katherine13,Beck Rachel13,Atkocius Andrew13,Qaium Faridi4,Luo Jingqin5,Michalski Jeff M.34,Picus Joel13,Pachynski Russell K.13,Maher Christopher A.1236,Chaudhuri Aadel A.34678

Affiliation:

1. Division of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO

2. McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO

3. Siteman Cancer Center, Barnes Jewish Hospital and Washington University School of Medicine, St Louis, MO

4. Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St Louis, MO

5. Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St Louis, MO

6. Department of Biomedical Engineering, Washington University School of Medicine, St Louis, MO

7. Department of Genetics, Washington University School of Medicine, St Louis, MO

8. Department of Computer Science and Engineering, Washington University in St Louis, St Louis, MO

Abstract

PURPOSE Cell-free DNA (cfDNA) and circulating tumor cell (CTC)–based liquid biopsies have emerged as potential tools to predict responses to androgen receptor (AR)–directed therapy in metastatic prostate cancer. However, because of complex mechanisms and incomplete understanding of genomic events involved in metastatic prostate cancer resistance, current assays (eg, CTC AR-V7) demonstrate low sensitivity and remain underutilized. The recent discovery of AR enhancer amplification in > 80% of patients with metastatic disease and its association with disease resistance presents an opportunity to improve on current assays. We hypothesized that tracking AR/enhancer genomic alterations in plasma cfDNA would detect resistance with high sensitivity and specificity. PATIENTS AND METHODS We developed a targeted sequencing and analysis method as part of a new assay called Enhancer and Neighboring Loci of Androgen Receptor Sequencing (EnhanceAR-Seq). We applied EnhanceAR-Seq to plasma collected from 40 patients with metastatic prostate cancer treated with AR-directed therapy to monitor AR/enhancer genomic alterations and correlated these events with therapy resistance, progression-free survival (PFS), and overall survival (OS). RESULTS EnhanceAR-Seq identified genomic alterations in the AR/enhancer locus in 45% of cases, including a 40% rate of AR enhancer amplification. Patients with AR/enhancer alterations had significantly worse PFS and OS than those without (6-month PFS, 30% v 71%; P = .0002; 6-month OS, 59% v 100%; P = .0015). AR/enhancer alterations in plasma cfDNA detected 18 of 23 resistant cases (78%) and outperformed the CTC AR-V7 assay, which was also run on a subset of patients. CONCLUSION cfDNA-based AR locus alterations, including of the enhancer, are strongly associated with resistance to AR-directed therapy and significantly worse survival. cfDNA analysis using EnhanceAR-Seq may enable more precise risk stratification and personalized therapeutic approaches for metastatic prostate cancer.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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