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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 |
Appears in Collections: | Producción 2020 |
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