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A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia

Cancer-related anorexia/cachexia is known to be associated with worsened quality of life and survival; however, limited treatment options exist. Although megestrol acetate (MA) is often used off-label to stimulate appetite and improve anorexia/cachexia in patients with advanced cancers, the benefits...

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Autores principales: Lim, Yu Liang, Teoh, Seth En, Yaow, Clyve Yu Leon, Lin, Daryl Jimian, Masuda, Yoshio, Han, Ming Xuan, Yeo, Wee Song, Ng, Qin Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267332/
https://www.ncbi.nlm.nih.gov/pubmed/35807039
http://dx.doi.org/10.3390/jcm11133756
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author Lim, Yu Liang
Teoh, Seth En
Yaow, Clyve Yu Leon
Lin, Daryl Jimian
Masuda, Yoshio
Han, Ming Xuan
Yeo, Wee Song
Ng, Qin Xiang
author_facet Lim, Yu Liang
Teoh, Seth En
Yaow, Clyve Yu Leon
Lin, Daryl Jimian
Masuda, Yoshio
Han, Ming Xuan
Yeo, Wee Song
Ng, Qin Xiang
author_sort Lim, Yu Liang
collection PubMed
description Cancer-related anorexia/cachexia is known to be associated with worsened quality of life and survival; however, limited treatment options exist. Although megestrol acetate (MA) is often used off-label to stimulate appetite and improve anorexia/cachexia in patients with advanced cancers, the benefits are controversial. The present meta-analysis aimed to better elucidate the clinical benefits of MA in patients with cancer-related anorexia/cachexia. A systematic search of PubMed, EMBASE, OVID Medline, Clinicaltrials.gov, and Google Scholar databases found 23 clinical trials examining the use of MA in cancer-related anorexia. The available randomized, controlled trials were appraised using Version 2 of the Cochrane risk-of-bias tool (RoB 2) and they had moderate-to-high risk of bias. A total of eight studies provided sufficient data on weight change for meta-analysis. The studies were divided into high-dose treatment (>320 mg/day) and low-dose treatment (≤320 mg/day). The overall pooled mean change in weight among cancer patients treated with MA, regardless of dosage was 0.75 kg (95% CI = −1.64 to 3.15, τ(2) = 9.35, I(2) = 96%). Patients who received high-dose MA tended to have weight loss rather than weight gain. There were insufficient studies to perform a meta-analysis for the change in tricep skinfold, midarm circumference, or quality of life measures. MA was generally well-tolerated, except for a clear thromboembolic risk, especially with higher doses. On balance, MA did not appear to be effective in providing the symptomatic improvement of anorexia/cachexia in patients with advanced cancer.
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spelling pubmed-92673322022-07-09 A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia Lim, Yu Liang Teoh, Seth En Yaow, Clyve Yu Leon Lin, Daryl Jimian Masuda, Yoshio Han, Ming Xuan Yeo, Wee Song Ng, Qin Xiang J Clin Med Review Cancer-related anorexia/cachexia is known to be associated with worsened quality of life and survival; however, limited treatment options exist. Although megestrol acetate (MA) is often used off-label to stimulate appetite and improve anorexia/cachexia in patients with advanced cancers, the benefits are controversial. The present meta-analysis aimed to better elucidate the clinical benefits of MA in patients with cancer-related anorexia/cachexia. A systematic search of PubMed, EMBASE, OVID Medline, Clinicaltrials.gov, and Google Scholar databases found 23 clinical trials examining the use of MA in cancer-related anorexia. The available randomized, controlled trials were appraised using Version 2 of the Cochrane risk-of-bias tool (RoB 2) and they had moderate-to-high risk of bias. A total of eight studies provided sufficient data on weight change for meta-analysis. The studies were divided into high-dose treatment (>320 mg/day) and low-dose treatment (≤320 mg/day). The overall pooled mean change in weight among cancer patients treated with MA, regardless of dosage was 0.75 kg (95% CI = −1.64 to 3.15, τ(2) = 9.35, I(2) = 96%). Patients who received high-dose MA tended to have weight loss rather than weight gain. There were insufficient studies to perform a meta-analysis for the change in tricep skinfold, midarm circumference, or quality of life measures. MA was generally well-tolerated, except for a clear thromboembolic risk, especially with higher doses. On balance, MA did not appear to be effective in providing the symptomatic improvement of anorexia/cachexia in patients with advanced cancer. MDPI 2022-06-28 /pmc/articles/PMC9267332/ /pubmed/35807039 http://dx.doi.org/10.3390/jcm11133756 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lim, Yu Liang
Teoh, Seth En
Yaow, Clyve Yu Leon
Lin, Daryl Jimian
Masuda, Yoshio
Han, Ming Xuan
Yeo, Wee Song
Ng, Qin Xiang
A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title_full A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title_fullStr A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title_full_unstemmed A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title_short A Systematic Review and Meta-Analysis of the Clinical Use of Megestrol Acetate for Cancer-Related Anorexia/Cachexia
title_sort systematic review and meta-analysis of the clinical use of megestrol acetate for cancer-related anorexia/cachexia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267332/
https://www.ncbi.nlm.nih.gov/pubmed/35807039
http://dx.doi.org/10.3390/jcm11133756
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