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Induction and maintenance of remission with mycophenolate mofetil in ANCA-associated vasculitis: a systematic review and meta-analysis

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dc.contributor.authorBerti, Alvise-
dc.contributor.authorAlsawas, Mouaz-
dc.contributor.authorJawaid, Tabinda-
dc.contributor.authorProkop, Larry J.-
dc.contributor.authorLee, Jiwon M.-
dc.contributor.authorJeong, Gwang Hun-
dc.contributor.authorQuintana, Luis F.-
dc.contributor.authorMoiseev, Sergey-
dc.contributor.authorVaglio, August-
dc.contributor.authorTesar, Vladimir-
dc.contributor.authorGeetha, Duvuru-
dc.contributor.authorShin, Jae Il-
dc.contributor.authorKronbichler, Andreas-
dc.date.accessioned2024-12-02T21:00:51Z-
dc.date.available2024-12-02T21:00:51Z-
dc.date.issued2022-10-
dc.identifier.issn0931-0509-
dc.identifier.issn1460-2385-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/71708-
dc.description.abstractBackground Uncertainties exist about the use of mycophenolate mofetil (MMF) in anti-neutrophil cytoplasmatic antibody (ANCA)-associated vasculitis (AAV), particularly for remission maintenance. Methods Systematic review and meta-analysis of phase II and III trials assessing the use of MMF in AAV, granulomatosis with polyangiitis and microscopic polyangiitis (MPA). A comprehensive search of several databases (Medline, EMBASE, Cochrane, Web of Science, Scopus) from inception to 5 May 2020 has been conducted. Trial data were extracted to estimate odds ratios (ORs) and estimates (ES) for MMF efficacy (remission-induction and maintenance). Severe adverse effects (SAEs) were collected. Results From 565 articles captured, 10 met the predefined criteria, 5 phase II and 5 III trials; 4 assessed remission-induction, 3 remission maintenance and 3 both. The pooled OR for remission-induction at 6 months was 1.06 (95% confidence interval 0.74, 1.52), with no significant difference by subgroup meta-analysis of trials stratified by different study-level features (i.e. kidney disease, MPA, myeloperoxidase-ANCA positivity, newly diagnosed disease) (P > 0.05). The overall ES for remission maintenance at the end of follow-up ranged between 51% and 91% (I-2 = 74.8%). Subgroup meta-analysis identified kidney involvement as a possible source of heterogeneity, yielding a significantly higher rate of sustained remission in trials enrolling only patients with kidney involvement (92%, 76-100%) versus those enrolling patients with and without kidney involvement (56%, 45-66%). Results were similar in multiple sensitivity analyses. During follow-up, the frequency of SAEs in MMF-based treatment arms was 31.8%. Conclusions In AAV, MMF use was significantly associated with higher sustained remission rates in trials enrolling only patients with kidney involvement. These findings might influence clinical practice.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherOxford University Press-
dc.titleInduction and maintenance of remission with mycophenolate mofetil in ANCA-associated vasculitis: a systematic review and meta-analysis-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1093/ndt/gfab357-
dc.identifier.scopusid2-s2.0-85140416119-
dc.identifier.wosid000764853000001-
dc.identifier.bibliographicCitationNephrology Dialysis Transplantation, v.37, no.11, pp 2190 - 2200-
dc.citation.titleNephrology Dialysis Transplantation-
dc.citation.volume37-
dc.citation.number11-
dc.citation.startPage2190-
dc.citation.endPage2200-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaTransplantation-
dc.relation.journalResearchAreaUrology & Nephrology-
dc.relation.journalWebOfScienceCategoryTransplantation-
dc.relation.journalWebOfScienceCategoryUrology & Nephrology-
dc.subject.keywordPlusANTIBODY-ASSOCIATED VASCULITIS-
dc.subject.keywordPlusCYCLOPHOSPHAMIDE-
dc.subject.keywordPlusAZATHIOPRINE-
dc.subject.keywordPlusRITUXIMAB-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusGLUCOCORTICOIDS-
dc.subject.keywordAuthorANCA-associated vasculitis-
dc.subject.keywordAuthorgranulomatosis with polyangiitis-
dc.subject.keywordAuthormicroscopic polyangiitis-
dc.subject.keywordAuthorMMF-
dc.subject.keywordAuthormycophenolate mofetil-
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