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Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers
BACKGROUND: Loss of PTEN is a common genomic aberration in castration-resistant prostate cancer (CRPC) and is frequently concurrent with ERG rearrangements, causing resistance to next-generation hormonal treatment (NGHT) including abiraterone. The relationship between PTEN loss and docetaxel sensiti...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995869/ https://www.ncbi.nlm.nih.gov/pubmed/29911685 http://dx.doi.org/10.1016/j.euo.2018.02.006 |
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author | Rescigno, Pasquale Lorente, David Dolling, David Ferraldeschi, Roberta Rodrigues, Daniel Nava Riisnaes, Ruth Miranda, Susana Bianchini, Diletta Zafeiriou, Zafeiris Sideris, Spyridon Ferreira, Ana Figueiredo, Ines Sumanasuriya, Semini Mateo, Joaquin Perez-Lopez, Raquel Sharp, Adam Tunariu, Nina de Bono, Johann S. |
author_facet | Rescigno, Pasquale Lorente, David Dolling, David Ferraldeschi, Roberta Rodrigues, Daniel Nava Riisnaes, Ruth Miranda, Susana Bianchini, Diletta Zafeiriou, Zafeiris Sideris, Spyridon Ferreira, Ana Figueiredo, Ines Sumanasuriya, Semini Mateo, Joaquin Perez-Lopez, Raquel Sharp, Adam Tunariu, Nina de Bono, Johann S. |
author_sort | Rescigno, Pasquale |
collection | PubMed |
description | BACKGROUND: Loss of PTEN is a common genomic aberration in castration-resistant prostate cancer (CRPC) and is frequently concurrent with ERG rearrangements, causing resistance to next-generation hormonal treatment (NGHT) including abiraterone. The relationship between PTEN loss and docetaxel sensitivity remains uncertain. OBJECTIVE: To study the antitumor activity of docetaxel in metastatic CRPC in relation to PTEN and ERG aberrations. DESIGN, SETTING, AND PARTICIPANTS: Single-centre, retrospective analysis of PTEN loss and ERG expression using a previously described immunohistochemistry (IHC) binary classification system. Patients received docetaxel between January 1, 2006 and July 31, 2016. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Response correlations were analyzed using Pearson's χ(2) tests and independent-sample t tests. Overall (OS) and progression-free survival (PFS) were analyzed using univariate and multivariate (MVA) Cox regression and Kaplan-Meier methods. RESULTS AND LIMITATIONS: Overall, 215 patients were eligible. Established metastatic CRPC prognostic factors were well balanced between PTEN loss (39%) and normal patients (61%). PTEN loss was associated with shorter median OS (25.4 vs 34.7 mo; hazard ratio [HR] 1.66, 95% confidence interval [CI] 1.18–2.13; p = 0.001). There were no differences in median PFS (8.0 vs 9.1 mo; univariate HR 1.20, 95% CI 0.86–1.68; p = 0.28) and PSA response (53.4% vs 50.6%; p = 0.74). PTEN loss was an independent prognostics factor in MVA. ERG status was available for 100 patients. ERG positivity was not associated with OS or PFS. Limitations include the retrospective nature and the single-centre analysis. CONCLUSIONS: Our findings suggest that metastatic CRPC with PTEN loss might benefit more from docetaxel than from NGHT. PATIENT SUMMARY: In this study we found that metastatic prostate cancer with loss of the PTEN switch may benefit more from docetaxel than from abiraterone. |
format | Online Article Text |
id | pubmed-5995869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-59958692018-06-13 Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers Rescigno, Pasquale Lorente, David Dolling, David Ferraldeschi, Roberta Rodrigues, Daniel Nava Riisnaes, Ruth Miranda, Susana Bianchini, Diletta Zafeiriou, Zafeiris Sideris, Spyridon Ferreira, Ana Figueiredo, Ines Sumanasuriya, Semini Mateo, Joaquin Perez-Lopez, Raquel Sharp, Adam Tunariu, Nina de Bono, Johann S. Eur Urol Oncol Article BACKGROUND: Loss of PTEN is a common genomic aberration in castration-resistant prostate cancer (CRPC) and is frequently concurrent with ERG rearrangements, causing resistance to next-generation hormonal treatment (NGHT) including abiraterone. The relationship between PTEN loss and docetaxel sensitivity remains uncertain. OBJECTIVE: To study the antitumor activity of docetaxel in metastatic CRPC in relation to PTEN and ERG aberrations. DESIGN, SETTING, AND PARTICIPANTS: Single-centre, retrospective analysis of PTEN loss and ERG expression using a previously described immunohistochemistry (IHC) binary classification system. Patients received docetaxel between January 1, 2006 and July 31, 2016. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Response correlations were analyzed using Pearson's χ(2) tests and independent-sample t tests. Overall (OS) and progression-free survival (PFS) were analyzed using univariate and multivariate (MVA) Cox regression and Kaplan-Meier methods. RESULTS AND LIMITATIONS: Overall, 215 patients were eligible. Established metastatic CRPC prognostic factors were well balanced between PTEN loss (39%) and normal patients (61%). PTEN loss was associated with shorter median OS (25.4 vs 34.7 mo; hazard ratio [HR] 1.66, 95% confidence interval [CI] 1.18–2.13; p = 0.001). There were no differences in median PFS (8.0 vs 9.1 mo; univariate HR 1.20, 95% CI 0.86–1.68; p = 0.28) and PSA response (53.4% vs 50.6%; p = 0.74). PTEN loss was an independent prognostics factor in MVA. ERG status was available for 100 patients. ERG positivity was not associated with OS or PFS. Limitations include the retrospective nature and the single-centre analysis. CONCLUSIONS: Our findings suggest that metastatic CRPC with PTEN loss might benefit more from docetaxel than from NGHT. PATIENT SUMMARY: In this study we found that metastatic prostate cancer with loss of the PTEN switch may benefit more from docetaxel than from abiraterone. Elsevier 2018-05 /pmc/articles/PMC5995869/ /pubmed/29911685 http://dx.doi.org/10.1016/j.euo.2018.02.006 Text en © 2018 Elsevier B.V. on behalf of European Association of Urology. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Rescigno, Pasquale Lorente, David Dolling, David Ferraldeschi, Roberta Rodrigues, Daniel Nava Riisnaes, Ruth Miranda, Susana Bianchini, Diletta Zafeiriou, Zafeiris Sideris, Spyridon Ferreira, Ana Figueiredo, Ines Sumanasuriya, Semini Mateo, Joaquin Perez-Lopez, Raquel Sharp, Adam Tunariu, Nina de Bono, Johann S. Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title | Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title_full | Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title_fullStr | Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title_full_unstemmed | Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title_short | Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers |
title_sort | docetaxel treatment in pten- and erg-aberrant metastatic prostate cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995869/ https://www.ncbi.nlm.nih.gov/pubmed/29911685 http://dx.doi.org/10.1016/j.euo.2018.02.006 |
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