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Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review

BACKGROUND: Biotherapy is becoming increasingly important in the treatment of adult-onset Still’s disease (AOSD). The aim of our study was to evaluate the efficacy and safety of biological therapy for AOSD resistant to traditional therapy. PATIENTS AND METHODS: Database of Library of Congress, the P...

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Autores principales: Zhou, Sha, Qiao, Jianjun, Bai, Juan, Wu, Yinhua, Fang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790106/
https://www.ncbi.nlm.nih.gov/pubmed/29416343
http://dx.doi.org/10.2147/TCRM.S155488
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author Zhou, Sha
Qiao, Jianjun
Bai, Juan
Wu, Yinhua
Fang, Hong
author_facet Zhou, Sha
Qiao, Jianjun
Bai, Juan
Wu, Yinhua
Fang, Hong
author_sort Zhou, Sha
collection PubMed
description BACKGROUND: Biotherapy is becoming increasingly important in the treatment of adult-onset Still’s disease (AOSD). The aim of our study was to evaluate the efficacy and safety of biological therapy for AOSD resistant to traditional therapy. PATIENTS AND METHODS: Database of Library of Congress, the PubMed, and Web of Science Core Collection were used to retrieve relevant articles published in English language until March 2017. Only studies published in English language were included, and the additional references quoted in these articles were also checked. Articles concerning the efficacy and safety of all the biotherapies in refractory AOSD were evaluated. RESULTS: There were 112 articles available in total; 422 AOSD patients were given at least one biologic. We found that 293 patients (69.43%) had received TNF-α blocking agents (infiliximab, etanercept, and adalimumab), 194 patients (45.97%) were treated with IL-1 receptor antagonists (anakinra, rilonacept, and canakinumab), 163 patients (38.63%) were given IL-6 inhibitor (tocilizumab), and 24 patients (5.69%) received rituximab and abatacept. The efficacy of biological therapy and overall tolerance of biological therapy for refractory AOSD were good. Thirty two of 271 patients given anti-TNF-α therapies (11.81%), 116 patients receiving IL-1 inhibitors (65.54%), 124 patients receiving tocilizumab (76.07%), and 13 patients given other biological therapies (36.11%) achieved remission. Side effects of biologic therapy were infections such as urinary tract infections and soft tissue abscess. CONCLUSION: Our findings suggest that anakinra and tocilizumab may be good choices for the treatment of refractory AOSD considering the effectiveness and safety.
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spelling pubmed-57901062018-02-07 Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review Zhou, Sha Qiao, Jianjun Bai, Juan Wu, Yinhua Fang, Hong Ther Clin Risk Manag Review BACKGROUND: Biotherapy is becoming increasingly important in the treatment of adult-onset Still’s disease (AOSD). The aim of our study was to evaluate the efficacy and safety of biological therapy for AOSD resistant to traditional therapy. PATIENTS AND METHODS: Database of Library of Congress, the PubMed, and Web of Science Core Collection were used to retrieve relevant articles published in English language until March 2017. Only studies published in English language were included, and the additional references quoted in these articles were also checked. Articles concerning the efficacy and safety of all the biotherapies in refractory AOSD were evaluated. RESULTS: There were 112 articles available in total; 422 AOSD patients were given at least one biologic. We found that 293 patients (69.43%) had received TNF-α blocking agents (infiliximab, etanercept, and adalimumab), 194 patients (45.97%) were treated with IL-1 receptor antagonists (anakinra, rilonacept, and canakinumab), 163 patients (38.63%) were given IL-6 inhibitor (tocilizumab), and 24 patients (5.69%) received rituximab and abatacept. The efficacy of biological therapy and overall tolerance of biological therapy for refractory AOSD were good. Thirty two of 271 patients given anti-TNF-α therapies (11.81%), 116 patients receiving IL-1 inhibitors (65.54%), 124 patients receiving tocilizumab (76.07%), and 13 patients given other biological therapies (36.11%) achieved remission. Side effects of biologic therapy were infections such as urinary tract infections and soft tissue abscess. CONCLUSION: Our findings suggest that anakinra and tocilizumab may be good choices for the treatment of refractory AOSD considering the effectiveness and safety. Dove Medical Press 2018-01-24 /pmc/articles/PMC5790106/ /pubmed/29416343 http://dx.doi.org/10.2147/TCRM.S155488 Text en © 2018 Zhou et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Zhou, Sha
Qiao, Jianjun
Bai, Juan
Wu, Yinhua
Fang, Hong
Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title_full Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title_fullStr Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title_full_unstemmed Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title_short Biological therapy of traditional therapy-resistant adult-onset Still’s disease: an evidence-based review
title_sort biological therapy of traditional therapy-resistant adult-onset still’s disease: an evidence-based review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790106/
https://www.ncbi.nlm.nih.gov/pubmed/29416343
http://dx.doi.org/10.2147/TCRM.S155488
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