Please use this identifier to cite or link to this item: http://hdl.handle.net/10668/11171
Title: Androgen receptor gene status in plasma DNA associates with worse outcome on enzalutamide or abiraterone for castration-resistant prostate cancer: a multi-institution correlative biomarker study.
Authors: Conteduca, V
Wetterskog, D
Sharabiani, M T A
Grande, E
Fernandez-Perez, M P
Jayaram, A
Salvi, S
Castellano, D
Romanel, A
Lolli, C
Casadio, V
Gurioli, G
Amadori, D
Font, A
Vazquez-Estevez, S
González Del Alba, A
Mellado, B
Fernandez-Calvo, O
Méndez-Vidal, M J
Climent, M A
Duran, I
Gallardo, E
Rodriguez, A
Santander, C
Sáez, M I
Puente, J
Gasi Tandefelt, D
Wingate, A
Dearnaley, D
PREMIERE Collaborators
Spanish Oncology Genitourinary Group
Demichelis, F
De Giorgi, U
Gonzalez-Billalabeitia, E
Attard, G
Keywords: abiraterone;androgen receptor;biomarker;castration-resistant prostate cancer;enzalutamide;plasma DNA
metadata.dc.subject.mesh: Adult
Aged
Aged, 80 and over
Androstenes
Antineoplastic Agents, Hormonal
Benzamides
Biomarkers, Tumor
Circulating Tumor DNA
DNA Mutational Analysis
Disease Progression
Disease-Free Survival
Europe
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Multiplex Polymerase Chain Reaction
Multivariate Analysis
Mutation
Nitriles
Odds Ratio
Patient Selection
Phenylthiohydantoin
Precision Medicine
Predictive Value of Tests
Proportional Hazards Models
Prospective Studies
Prostatic Neoplasms, Castration-Resistant
Receptors, Androgen
Risk Factors
Time Factors
Treatment Outcome
Issue Date: 2017
Abstract: There is an urgent need to identify biomarkers to guide personalized therapy in castration-resistant prostate cancer (CRPC). We aimed to clinically qualify androgen receptor (AR) gene status measurement in plasma DNA using multiplex droplet digital PCR (ddPCR) in pre- and post-chemotherapy CRPC. We optimized ddPCR assays for AR copy number and mutations and retrospectively analyzed plasma DNA from patients recruited to one of the three biomarker protocols with prospectively collected clinical data. We evaluated associations between plasma AR and overall survival (OS) and progression-free survival (PFS) in 73 chemotherapy-naïve and 98 post-docetaxel CRPC patients treated with enzalutamide or abiraterone (Primary cohort) and 94 chemotherapy-naïve patients treated with enzalutamide (Secondary cohort; PREMIERE trial). In the primary cohort, AR gain was observed in 10 (14%) chemotherapy-naïve and 33 (34%) post-docetaxel patients and associated with worse OS [hazard ratio (HR), 3.98; 95% CI 1.74-9.10; P A (p.L702H) and 2632A>G (p.T878A)] were observed in eight (11%) post-docetaxel but no chemotherapy-naïve abiraterone-treated patients and were also associated with worse OS (HR 3.26; 95% CI 1.47-not reached; P = 0.004). There was no interaction between AR and docetaxel status (P = 0.83 for OS, P = 0.99 for PFS). In the PREMIERE trial, 11 patients (12%) with AR gain had worse PSA-PFS (sPFS) (HR 4.33; 95% CI 1.94-9.68; P G (p.T878A)] were observed in eight (11%) post-docetaxel but no chemotherapy-naïve abiraterone-treated patients and were also associated with worse OS (HR 3.26; 95% CI 1.47-not reached; P = 0.004). There was no interaction between AR and docetaxel status (P = 0.83 for OS, P = 0.99 for PFS). In the PREMIERE trial, 11 patients (12%) with AR gain had worse PSA-PFS (sPFS) (HR 4.33; 95% CI 1.94-9.68; P  Plasma AR status assessment using ddPCR identifies CRPC with worse outcome to enzalutamide or abiraterone. Prospective evaluation of treatment decisions based on plasma AR is now required. NCT02288936 (PREMIERE trial).
URI: http://hdl.handle.net/10668/11171
metadata.dc.identifier.doi: 10.1093/annonc/mdx155
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