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Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer

Plasma androgen receptor (AR) gain identifies metastatic castration-resistant prostate cancer (mCRPC) patients with worse outcome on abiraterone/enzalutamide, but its relevance in the context of taxane chemotherapy is unknown. We aimed to evaluate whether docetaxel is active regardless of plasma AR...

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Autores principales: Conteduca, Vincenza, Jayaram, Anuradha, Romero-Laorden, Nuria, Wetterskog, Daniel, Salvi, Samanta, Gurioli, Giorgia, Scarpi, Emanuela, Castro, Elena, Marin-Aguilera, Mercedes, Lolli, Cristian, Schepisi, Giuseppe, Maugeri, Antonio, Wingate, Anna, Farolfi, Alberto, Casadio, Valentina, Medina, Ana, Puente, Javier, Vidal, Mª José Méndez, Morales-Barrera, Rafael, Villa-Guzmán, Jose C., Hernando, Susana, Rodriguez-Vida, Alejo, González-del-Alba, Aránzazu, Mellado, Begoña, Gonzalez-Billalabeitia, Enrique, Olmos, David, Attard, Gerhardt, De Giorgi, Ugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377278/
https://www.ncbi.nlm.nih.gov/pubmed/30773204
http://dx.doi.org/10.1016/j.eururo.2018.09.049
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author Conteduca, Vincenza
Jayaram, Anuradha
Romero-Laorden, Nuria
Wetterskog, Daniel
Salvi, Samanta
Gurioli, Giorgia
Scarpi, Emanuela
Castro, Elena
Marin-Aguilera, Mercedes
Lolli, Cristian
Schepisi, Giuseppe
Maugeri, Antonio
Wingate, Anna
Farolfi, Alberto
Casadio, Valentina
Medina, Ana
Puente, Javier
Vidal, Mª José Méndez
Morales-Barrera, Rafael
Villa-Guzmán, Jose C.
Hernando, Susana
Rodriguez-Vida, Alejo
González-del-Alba, Aránzazu
Mellado, Begoña
Gonzalez-Billalabeitia, Enrique
Olmos, David
Attard, Gerhardt
De Giorgi, Ugo
author_facet Conteduca, Vincenza
Jayaram, Anuradha
Romero-Laorden, Nuria
Wetterskog, Daniel
Salvi, Samanta
Gurioli, Giorgia
Scarpi, Emanuela
Castro, Elena
Marin-Aguilera, Mercedes
Lolli, Cristian
Schepisi, Giuseppe
Maugeri, Antonio
Wingate, Anna
Farolfi, Alberto
Casadio, Valentina
Medina, Ana
Puente, Javier
Vidal, Mª José Méndez
Morales-Barrera, Rafael
Villa-Guzmán, Jose C.
Hernando, Susana
Rodriguez-Vida, Alejo
González-del-Alba, Aránzazu
Mellado, Begoña
Gonzalez-Billalabeitia, Enrique
Olmos, David
Attard, Gerhardt
De Giorgi, Ugo
author_sort Conteduca, Vincenza
collection PubMed
description Plasma androgen receptor (AR) gain identifies metastatic castration-resistant prostate cancer (mCRPC) patients with worse outcome on abiraterone/enzalutamide, but its relevance in the context of taxane chemotherapy is unknown. We aimed to evaluate whether docetaxel is active regardless of plasma AR and to perform an exploratory analysis to compare docetaxel with abiraterone/enzalutamide. This multi-institutional study was a pooled analysis of AR status, determined by droplet digital polymerase chain reaction, on pretreatment plasma samples. We evaluated associations between plasma AR and overall/progression-free survival (OS/PFS) and prostate-specific antigen (PSA) response rate in 163 docetaxel-treated patients. OS was significantly shorter in case of AR gain (hazard ratio [HR] = 1.61, 95% confidence interval [CI] = 1.08–2.39, p = 0.018), but not PFS (HR = 1.04, 95% CI 0.74–1.46, p = 0.8) or PSA response (odds ratio = 1.14, 95% CI = 0.65–1.99, p = 0.7). We investigated the interaction between plasma AR and treatment type after incorporating updated data from our prior study of 73 chemotherapy-naïve, abiraterone/enzalutamide-treated patients, with data from 115 first-line docetaxel patients. In an exploratory analysis of mCRPC patients receiving first-line therapies, a significant interaction was observed between plasma AR and docetaxel versus abiraterone/enzalutamide for OS (HR = 0.16, 95% CI = 0.06–0.46, p < 0.001) and PFS (HR = 0.31, 95% CI = 0.12–0.80, p = 0.02). Specifically, we reported a significant difference for OS favoring abiraterone/enzalutamide for AR-normal patients (HR = 1.93, 95% CI = 1.19–3.12, p = 0.008) and a suggestion favoring docetaxel for AR-gained patients (HR = 0.53, 95% CI = 0.24–1.16, p = 0.11). These data suggest that AR-normal patients should receive abiraterone/enzalutamide and AR-gained could benefit from docetaxel. This treatment selection merits prospective evaluation in a randomized trial. PATIENT SUMMARY: We investigated whether plasma androgen receptor (AR) predicted outcome in metastatic castration-resistant prostate cancer (mCRPC) patients treated with docetaxel, and we performed an exploratory analysis in patients treated with docetaxel or AR-directed drugs as first-line mCRPC therapy. We showed that plasma AR normal favored hormonal treatment, whilst plasma AR-gained patients may have had a longer response to docetaxel, suggesting that plasma AR status could be a useful treatment selection biomarker.
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spelling pubmed-63772782019-03-01 Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer Conteduca, Vincenza Jayaram, Anuradha Romero-Laorden, Nuria Wetterskog, Daniel Salvi, Samanta Gurioli, Giorgia Scarpi, Emanuela Castro, Elena Marin-Aguilera, Mercedes Lolli, Cristian Schepisi, Giuseppe Maugeri, Antonio Wingate, Anna Farolfi, Alberto Casadio, Valentina Medina, Ana Puente, Javier Vidal, Mª José Méndez Morales-Barrera, Rafael Villa-Guzmán, Jose C. Hernando, Susana Rodriguez-Vida, Alejo González-del-Alba, Aránzazu Mellado, Begoña Gonzalez-Billalabeitia, Enrique Olmos, David Attard, Gerhardt De Giorgi, Ugo Eur Urol Article Plasma androgen receptor (AR) gain identifies metastatic castration-resistant prostate cancer (mCRPC) patients with worse outcome on abiraterone/enzalutamide, but its relevance in the context of taxane chemotherapy is unknown. We aimed to evaluate whether docetaxel is active regardless of plasma AR and to perform an exploratory analysis to compare docetaxel with abiraterone/enzalutamide. This multi-institutional study was a pooled analysis of AR status, determined by droplet digital polymerase chain reaction, on pretreatment plasma samples. We evaluated associations between plasma AR and overall/progression-free survival (OS/PFS) and prostate-specific antigen (PSA) response rate in 163 docetaxel-treated patients. OS was significantly shorter in case of AR gain (hazard ratio [HR] = 1.61, 95% confidence interval [CI] = 1.08–2.39, p = 0.018), but not PFS (HR = 1.04, 95% CI 0.74–1.46, p = 0.8) or PSA response (odds ratio = 1.14, 95% CI = 0.65–1.99, p = 0.7). We investigated the interaction between plasma AR and treatment type after incorporating updated data from our prior study of 73 chemotherapy-naïve, abiraterone/enzalutamide-treated patients, with data from 115 first-line docetaxel patients. In an exploratory analysis of mCRPC patients receiving first-line therapies, a significant interaction was observed between plasma AR and docetaxel versus abiraterone/enzalutamide for OS (HR = 0.16, 95% CI = 0.06–0.46, p < 0.001) and PFS (HR = 0.31, 95% CI = 0.12–0.80, p = 0.02). Specifically, we reported a significant difference for OS favoring abiraterone/enzalutamide for AR-normal patients (HR = 1.93, 95% CI = 1.19–3.12, p = 0.008) and a suggestion favoring docetaxel for AR-gained patients (HR = 0.53, 95% CI = 0.24–1.16, p = 0.11). These data suggest that AR-normal patients should receive abiraterone/enzalutamide and AR-gained could benefit from docetaxel. This treatment selection merits prospective evaluation in a randomized trial. PATIENT SUMMARY: We investigated whether plasma androgen receptor (AR) predicted outcome in metastatic castration-resistant prostate cancer (mCRPC) patients treated with docetaxel, and we performed an exploratory analysis in patients treated with docetaxel or AR-directed drugs as first-line mCRPC therapy. We showed that plasma AR normal favored hormonal treatment, whilst plasma AR-gained patients may have had a longer response to docetaxel, suggesting that plasma AR status could be a useful treatment selection biomarker. Elsevier Science 2019-03 /pmc/articles/PMC6377278/ /pubmed/30773204 http://dx.doi.org/10.1016/j.eururo.2018.09.049 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Conteduca, Vincenza
Jayaram, Anuradha
Romero-Laorden, Nuria
Wetterskog, Daniel
Salvi, Samanta
Gurioli, Giorgia
Scarpi, Emanuela
Castro, Elena
Marin-Aguilera, Mercedes
Lolli, Cristian
Schepisi, Giuseppe
Maugeri, Antonio
Wingate, Anna
Farolfi, Alberto
Casadio, Valentina
Medina, Ana
Puente, Javier
Vidal, Mª José Méndez
Morales-Barrera, Rafael
Villa-Guzmán, Jose C.
Hernando, Susana
Rodriguez-Vida, Alejo
González-del-Alba, Aránzazu
Mellado, Begoña
Gonzalez-Billalabeitia, Enrique
Olmos, David
Attard, Gerhardt
De Giorgi, Ugo
Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title_full Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title_fullStr Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title_full_unstemmed Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title_short Plasma Androgen Receptor and Docetaxel for Metastatic Castration-resistant Prostate Cancer
title_sort plasma androgen receptor and docetaxel for metastatic castration-resistant prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377278/
https://www.ncbi.nlm.nih.gov/pubmed/30773204
http://dx.doi.org/10.1016/j.eururo.2018.09.049
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