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Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis

OBJECTIVE: Most comprehensive treatments for PBC include UDCA, combination of methotrexate (MTX), corticosteroids (COT), colchicine (COC) or bezafibrate (BEF), cyclosporin A (CYP), D-penicillamine (DPM), methotrexate (MTX), or azathioprine (AZP). Since the optimum treatment regimen remains inconclus...

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Autores principales: Zhu, Gui-Qi, Huang, Sha, Huang, Gui-Qian, Wang, Li-Ren, Lin, Yi-Qian, Wu, Yi-Ming, Shi, Ke-Qing, Wang, Jiang-Tao, Zhou, Zhi-Rui, Braddock, Martin, Chen, Yong-Ping, Zhou, Meng-Tao, Zheng, Ming-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695204/
https://www.ncbi.nlm.nih.gov/pubmed/26109432
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author Zhu, Gui-Qi
Huang, Sha
Huang, Gui-Qian
Wang, Li-Ren
Lin, Yi-Qian
Wu, Yi-Ming
Shi, Ke-Qing
Wang, Jiang-Tao
Zhou, Zhi-Rui
Braddock, Martin
Chen, Yong-Ping
Zhou, Meng-Tao
Zheng, Ming-Hua
author_facet Zhu, Gui-Qi
Huang, Sha
Huang, Gui-Qian
Wang, Li-Ren
Lin, Yi-Qian
Wu, Yi-Ming
Shi, Ke-Qing
Wang, Jiang-Tao
Zhou, Zhi-Rui
Braddock, Martin
Chen, Yong-Ping
Zhou, Meng-Tao
Zheng, Ming-Hua
author_sort Zhu, Gui-Qi
collection PubMed
description OBJECTIVE: Most comprehensive treatments for PBC include UDCA, combination of methotrexate (MTX), corticosteroids (COT), colchicine (COC) or bezafibrate (BEF), cyclosporin A (CYP), D-penicillamine (DPM), methotrexate (MTX), or azathioprine (AZP). Since the optimum treatment regimen remains inconclusive, we aimed to compare these therapies in terms of patient mortality or liver transplantation (MOLT) and adverse event (AE). METHODS: We searched PubMed, Embase, Scopus and the Cochrane Library for randomized controlled trials until August 2014. We estimated HRs for MOLT and ORs for AE. The sensitivity analysis based on dose of UDCA was also performed. RESULTS: The search identified 49 studies involving 12 different treatment regimens and 4182 patients. Although no statistical significance can be found in MOLT, COT plus UDCA was ranked highest for efficacy outcome amongst all the treatment regimes. While for AEs, compared with OBS or UDCA, monotherapy with COC (OR 5.6, P < 0.001; OR 5.89, P < 0.001), CYP (OR 3.24, P < 0.001; OR 3.42, P < 0.001), DPM (OR 8.00, P < 0.001; OR 8.45, P < 0.001) and MTX (OR 5.31, P < 0.001; OR 5.61, P < 0.001) were associated with statistically significant increased risk of AEs. No significant differences were found for other combination regimes. Effect estimates from indirect comparisons matched closely to estimates derived from pairwise comparisons. Consistently, in the sensitivity analysis, results closely resembled our primary analysis. CONCLUSIONS: COT plus UDCA was the most efficacious among treatment regimens both for MOLT and AEs.
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spelling pubmed-46952042016-01-26 Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis Zhu, Gui-Qi Huang, Sha Huang, Gui-Qian Wang, Li-Ren Lin, Yi-Qian Wu, Yi-Ming Shi, Ke-Qing Wang, Jiang-Tao Zhou, Zhi-Rui Braddock, Martin Chen, Yong-Ping Zhou, Meng-Tao Zheng, Ming-Hua Oncotarget Clinical Research Paper OBJECTIVE: Most comprehensive treatments for PBC include UDCA, combination of methotrexate (MTX), corticosteroids (COT), colchicine (COC) or bezafibrate (BEF), cyclosporin A (CYP), D-penicillamine (DPM), methotrexate (MTX), or azathioprine (AZP). Since the optimum treatment regimen remains inconclusive, we aimed to compare these therapies in terms of patient mortality or liver transplantation (MOLT) and adverse event (AE). METHODS: We searched PubMed, Embase, Scopus and the Cochrane Library for randomized controlled trials until August 2014. We estimated HRs for MOLT and ORs for AE. The sensitivity analysis based on dose of UDCA was also performed. RESULTS: The search identified 49 studies involving 12 different treatment regimens and 4182 patients. Although no statistical significance can be found in MOLT, COT plus UDCA was ranked highest for efficacy outcome amongst all the treatment regimes. While for AEs, compared with OBS or UDCA, monotherapy with COC (OR 5.6, P < 0.001; OR 5.89, P < 0.001), CYP (OR 3.24, P < 0.001; OR 3.42, P < 0.001), DPM (OR 8.00, P < 0.001; OR 8.45, P < 0.001) and MTX (OR 5.31, P < 0.001; OR 5.61, P < 0.001) were associated with statistically significant increased risk of AEs. No significant differences were found for other combination regimes. Effect estimates from indirect comparisons matched closely to estimates derived from pairwise comparisons. Consistently, in the sensitivity analysis, results closely resembled our primary analysis. CONCLUSIONS: COT plus UDCA was the most efficacious among treatment regimens both for MOLT and AEs. Impact Journals LLC 2015-06-19 /pmc/articles/PMC4695204/ /pubmed/26109432 Text en Copyright: © 2015 Zhu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Zhu, Gui-Qi
Huang, Sha
Huang, Gui-Qian
Wang, Li-Ren
Lin, Yi-Qian
Wu, Yi-Ming
Shi, Ke-Qing
Wang, Jiang-Tao
Zhou, Zhi-Rui
Braddock, Martin
Chen, Yong-Ping
Zhou, Meng-Tao
Zheng, Ming-Hua
Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title_full Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title_fullStr Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title_full_unstemmed Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title_short Optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
title_sort optimal drug regimens for primary biliary cirrhosis: a systematic review and network meta-analysis
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695204/
https://www.ncbi.nlm.nih.gov/pubmed/26109432
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