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Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer
BACKGROUND: Standard medical castration reduces muscle mass. We sought to characterize body composition changes in men undergoing maximal androgen suppression with and without exogenous gluocorticoids. METHODS: Cross-sectional areas of total fat, visceral fat and muscle were measured on serial CT sc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721397/ https://www.ncbi.nlm.nih.gov/pubmed/23807167 http://dx.doi.org/10.1038/bjc.2013.340 |
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author | Pezaro, C Mukherji, D Tunariu, N Cassidy, A M Omlin, A Bianchini, D Seed, G Reid, A H M Olmos, D de Bono, J S Attard, G |
author_facet | Pezaro, C Mukherji, D Tunariu, N Cassidy, A M Omlin, A Bianchini, D Seed, G Reid, A H M Olmos, D de Bono, J S Attard, G |
author_sort | Pezaro, C |
collection | PubMed |
description | BACKGROUND: Standard medical castration reduces muscle mass. We sought to characterize body composition changes in men undergoing maximal androgen suppression with and without exogenous gluocorticoids. METHODS: Cross-sectional areas of total fat, visceral fat and muscle were measured on serial CT scans in a post-hoc analysis of patients treated in Phase I/II trials with abiraterone followed by abiraterone and dexamethasone 0.5 mg daily. Linear mixed regression models were used to account for variations in time-on-treatment and baseline body mass index (BMI). RESULTS: Fifty-five patients received a median of 7.5 months abiraterone followed by 5.4 months abiraterone and dexamethasone. Muscle loss was observed on single-agent abiraterone (maximal in patients with baseline BMI >30, −4.3%), but no further loss was observed after addition of dexamethasone. Loss of visceral fat was also observed on single-agent abiraterone, (baseline BMI >30 patients −19.6%). In contrast, addition of dexamethasone led to an increase in central visceral and total fat and BMI in all the patients. INTERPRETATION: Maximal androgen suppression was associated with loss of muscle and visceral fat. Addition of low dose dexamethasone resulted in significant increases in visceral and total fat. These changes could have important quality-of-life implications for men treated with abiraterone. |
format | Online Article Text |
id | pubmed-3721397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37213972014-07-23 Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer Pezaro, C Mukherji, D Tunariu, N Cassidy, A M Omlin, A Bianchini, D Seed, G Reid, A H M Olmos, D de Bono, J S Attard, G Br J Cancer Clinical Study BACKGROUND: Standard medical castration reduces muscle mass. We sought to characterize body composition changes in men undergoing maximal androgen suppression with and without exogenous gluocorticoids. METHODS: Cross-sectional areas of total fat, visceral fat and muscle were measured on serial CT scans in a post-hoc analysis of patients treated in Phase I/II trials with abiraterone followed by abiraterone and dexamethasone 0.5 mg daily. Linear mixed regression models were used to account for variations in time-on-treatment and baseline body mass index (BMI). RESULTS: Fifty-five patients received a median of 7.5 months abiraterone followed by 5.4 months abiraterone and dexamethasone. Muscle loss was observed on single-agent abiraterone (maximal in patients with baseline BMI >30, −4.3%), but no further loss was observed after addition of dexamethasone. Loss of visceral fat was also observed on single-agent abiraterone, (baseline BMI >30 patients −19.6%). In contrast, addition of dexamethasone led to an increase in central visceral and total fat and BMI in all the patients. INTERPRETATION: Maximal androgen suppression was associated with loss of muscle and visceral fat. Addition of low dose dexamethasone resulted in significant increases in visceral and total fat. These changes could have important quality-of-life implications for men treated with abiraterone. Nature Publishing Group 2013-07-23 2013-06-27 /pmc/articles/PMC3721397/ /pubmed/23807167 http://dx.doi.org/10.1038/bjc.2013.340 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Clinical Study Pezaro, C Mukherji, D Tunariu, N Cassidy, A M Omlin, A Bianchini, D Seed, G Reid, A H M Olmos, D de Bono, J S Attard, G Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title | Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title_full | Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title_fullStr | Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title_full_unstemmed | Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title_short | Sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
title_sort | sarcopenia and change in body composition following maximal androgen suppression with abiraterone in men with castration-resistant prostate cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721397/ https://www.ncbi.nlm.nih.gov/pubmed/23807167 http://dx.doi.org/10.1038/bjc.2013.340 |
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