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Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids

Aim to evaluate the efficacy and safety of glucocorticoid monotherapy vs combination therapy of cyclophosphamide (CYC) for IgG4 related disease (IgG4-RD). 102 newly diagnosed IgG4-RD patients were enrolled and assigned to 2 groups: Group I was prednisone monotherapy (0.5–1.0 mg/kg.d, tapered gradual...

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Autores principales: Yunyun, Fei, Yu, Chen, Panpan, Zhang, Hua, Chen, Di, Wu, Lidan, Zhao, Linyi, Peng, Li, Wang, Qingjun, Wu, Xuan, Zhang, Yan, Zhao, Xiaofeng, Zeng, Fengchun, Zhang, Wen, Zhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522435/
https://www.ncbi.nlm.nih.gov/pubmed/28733656
http://dx.doi.org/10.1038/s41598-017-06520-5
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author Yunyun, Fei
Yu, Chen
Panpan, Zhang
Hua, Chen
Di, Wu
Lidan, Zhao
Linyi, Peng
Li, Wang
Qingjun, Wu
Xuan, Zhang
Yan, Zhao
Xiaofeng, Zeng
Fengchun, Zhang
Wen, Zhang
author_facet Yunyun, Fei
Yu, Chen
Panpan, Zhang
Hua, Chen
Di, Wu
Lidan, Zhao
Linyi, Peng
Li, Wang
Qingjun, Wu
Xuan, Zhang
Yan, Zhao
Xiaofeng, Zeng
Fengchun, Zhang
Wen, Zhang
author_sort Yunyun, Fei
collection PubMed
description Aim to evaluate the efficacy and safety of glucocorticoid monotherapy vs combination therapy of cyclophosphamide (CYC) for IgG4 related disease (IgG4-RD). 102 newly diagnosed IgG4-RD patients were enrolled and assigned to 2 groups: Group I was prednisone monotherapy (0.5–1.0 mg/kg.d, tapered gradually) and Group II was glucocorticoid and CYC (50–100 mg per day). Patients were assessed at different periods. Primary end point was relapse rate; secondary end points included response, remission rate and adverse effects. 52 patients were in Group I and 50 in Group II. At 1 month, both groups achieved obvious improvement. Accumulated relapse rate during 1 year was 38.5% in Group 1, including 12 cases with clinical relapse and 8 patients manifesting only serological relapse; whereas there was 12.0% of relapse in Group 2, only 1 with clinical relapse and other 5 patients got serological relapse. The mean flare time in Group II was significantly longer than that in Group I. All relapsing patients in Group I were sensitive to immunosuppressants. Most patients involving more than 6 organs in Group I relapsed during 1 year. IgG4 levels of relapse cases were significantly higher than non-relapsing patients at baseline. Bile duct, lacrimal glands and lymph nodes were commonly relapsed organs in Group I.
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spelling pubmed-55224352017-07-26 Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids Yunyun, Fei Yu, Chen Panpan, Zhang Hua, Chen Di, Wu Lidan, Zhao Linyi, Peng Li, Wang Qingjun, Wu Xuan, Zhang Yan, Zhao Xiaofeng, Zeng Fengchun, Zhang Wen, Zhang Sci Rep Article Aim to evaluate the efficacy and safety of glucocorticoid monotherapy vs combination therapy of cyclophosphamide (CYC) for IgG4 related disease (IgG4-RD). 102 newly diagnosed IgG4-RD patients were enrolled and assigned to 2 groups: Group I was prednisone monotherapy (0.5–1.0 mg/kg.d, tapered gradually) and Group II was glucocorticoid and CYC (50–100 mg per day). Patients were assessed at different periods. Primary end point was relapse rate; secondary end points included response, remission rate and adverse effects. 52 patients were in Group I and 50 in Group II. At 1 month, both groups achieved obvious improvement. Accumulated relapse rate during 1 year was 38.5% in Group 1, including 12 cases with clinical relapse and 8 patients manifesting only serological relapse; whereas there was 12.0% of relapse in Group 2, only 1 with clinical relapse and other 5 patients got serological relapse. The mean flare time in Group II was significantly longer than that in Group I. All relapsing patients in Group I were sensitive to immunosuppressants. Most patients involving more than 6 organs in Group I relapsed during 1 year. IgG4 levels of relapse cases were significantly higher than non-relapsing patients at baseline. Bile duct, lacrimal glands and lymph nodes were commonly relapsed organs in Group I. Nature Publishing Group UK 2017-07-21 /pmc/articles/PMC5522435/ /pubmed/28733656 http://dx.doi.org/10.1038/s41598-017-06520-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yunyun, Fei
Yu, Chen
Panpan, Zhang
Hua, Chen
Di, Wu
Lidan, Zhao
Linyi, Peng
Li, Wang
Qingjun, Wu
Xuan, Zhang
Yan, Zhao
Xiaofeng, Zeng
Fengchun, Zhang
Wen, Zhang
Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title_full Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title_fullStr Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title_full_unstemmed Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title_short Efficacy of Cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids
title_sort efficacy of cyclophosphamide treatment for immunoglobulin g4-related disease with addition of glucocorticoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522435/
https://www.ncbi.nlm.nih.gov/pubmed/28733656
http://dx.doi.org/10.1038/s41598-017-06520-5
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