Abstract
Introduction: Plasma androgen receptor (AR) copy number (CN) status identifies castration-resistant prostate cancer (CRPC) patients with worse outcome on abiraterone/enzalutamide. However, the impact of AR CN changes on clinical outcome in CRPC is unknown.Materials and Methods: Plasma samples from 73 patients treated with abiraterone or enzalutamide were collected at baseline and at the time of progression disease (PD). Droplet digital polymerase chain reaction was used to assess AR CN status.Results: We showed that 11 patients (15.1%) changed AR CN status from baseline to PD (9 patients from normal to gain, 2 from gain to normal). Patients changing AR CN status from normal at baseline to gain at PD had intermediate median overall survival (OS) of 20.5 months (95% CI = 8.0–44.2) between those who remained AR CN normal from baseline to PD (27.3 months [95% CI = 21.9–34.4]) and those who remained AR CN gain from baseline to PD (9.1 months [95% CI = 3.8–14.5], p < 0.0001). Patients changing AR CN from normal at baseline to gain at PD had a median progression-free survival (PFS) of 9.2 months (95% CI = 2.0–14.7), patients who remained AR CN normal had a median PFS of 9.1 months (95% CI = 7.2–10.1), and patients who remained AR CN gain had a median PFS of 5.4 (95% CI = 3.6–6.5, p = 0.0005). Both OS and PFS were not significantly different between patients with AR CN that changes from normal to gain and patients with stable AR CN normal.Conclusions: We showed that CRPC patients changing AR CN status from baseline to progression time point had intermediate OS and we suggested that AR CN evaluation at baseline could be the most informative for clinical outcome of CRPC patients treated with abiraterone or enzalutamide. Larger prospective studies are warranted.
Highlights
Plasma androgen receptor (AR) copy number (CN) status identifies castration-resistant prostate cancer (CRPC) patients with worse outcome on abiraterone/enzalutamide
We evaluate the role of plasma Androgen receptor (AR) Copy number (CN) changes on clinical outcome in CRPC patients treated with abiraterone or enzalutamide
We found that 84% [49] of 58 patients with AR CN normal and 87% [13] of 15 with AR CN gain at baseline showed no changes in AR CN status in their Progression disease (PD) sample (Figure 1A), observing a 15.1% conversion rate of AR CN status from baseline to PD time point
Summary
Plasma androgen receptor (AR) copy number (CN) status identifies castration-resistant prostate cancer (CRPC) patients with worse outcome on abiraterone/enzalutamide. Abiraterone acetate and enzalutamide belong to therapies introduced in the past years for patients with metastatic castration-resistant prostate cancer (CRPC), improving patient survival and quality of life [1,2,3,4]. Cell free DNA (cfDNA) has emerged as a minimally invasive and good source of biomarkers deriving from multiple metastases, suggesting its role in monitoring clinical outcome and tumor heterogeneity [6,7,8]. We evaluate the role of plasma AR CN changes on clinical outcome in CRPC patients treated with abiraterone or enzalutamide
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