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dc.contributor.authorPugliesi, Alissones_ES
dc.contributor.authorBorges de Oliveira, Amandaes_ES
dc.contributor.authorOliveira, Ana Beatricees_ES
dc.contributor.authorXavier, Ricardoes_ES
dc.contributor.authorHenrique da Mota, Liciaes_ES
dc.contributor.authorBarros Bertolo, Manoeles_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.authorCitera, Gustavoes_ES
dc.contributor.authorFernandes de Carvalho, Luiz Sergioes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-10-30T16:31:22Z
dc.date.available2023-10-30T16:31:22Z
dc.date.issued2023es_ES
dc.identifier.issn2523-3106es_ES
dc.identifier.urihttps://hdl.handle.net/10902/30392
dc.description.abstractBackground Our aim was to compare the efcacy of rituximab, tocilizumab, and abatacept in individuals with rheu‑matoid arthritis (RA) refractory to treatments with MTX or TNFi agents. Methods We searched 6 databases until January 2023 for phase 2–4 RCTs evaluating patients with RA refractory to MTX or TNFi therapy treated with rituximab, abatacept, and tocilizumab (intervention arm) compared to controls. Study data were independently assessed by two investigators. The primary outcome was considered as achieving ACR70 response. Results The meta-analysis included 19 RCTs, with 7,835 patients and a mean study duration of 1.2 years. Hazard ratios for achieving an ACR70 response at six months were not diferent among the bDMARDs, however, we found high heterogeneity. Three factors showing a critical imbalance among the bDMARD classes were identifed: baseline HAQ score, study duration, and frequency of TNFi treatment in control arm. Multivariate meta-regression adjusted to these three factors were conducted for the relative risk (RR) for ACR70. Thus, heterogeneity was attenuated (I2=24%) and the explanatory power of the model increased (R2=85%). In this model, rituximab did not modify the chance of achieving an ACR70 response compared to abatacept (RR=1.773, 95%CI 0.113–10.21, p=0.765). In contrast, abatacept was associated with RR=2.217 (95%CI 1.554–3.161, p<0.001) for ACR70 compared to tocilizumab. Conclusion We found high heterogeneity among studies comparing rituximab, abatacept, and tocilizumab. On multivariate metaregressions, if the conditions of the RCTs were similar, we estimate that abatacept could increase the chance of reaching an ACR70 response by 2.2-fold compared to tocilizumab.es_ES
dc.description.sponsorshipFunding. This work was supported by grants 437413/2018–7 from the Brazilian National Research Council (CNPq) and 2019/09068–3 from São Paulo State Foundation for Research (FAPESP). Acknowledgements. We acknowledge all support received by Brazilian Society of Rheumatology.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution 4.0 International*
dc.rights© The Author(s) 2023es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceAdvances in Rheumatology, 2023, 63, 30es_ES
dc.subject.otherRheumatoid arthritises_ES
dc.subject.otherRituximabes_ES
dc.subject.otherAbataceptes_ES
dc.subject.otherTocilizumabes_ES
dc.subject.otherbDMARDes_ES
dc.subject.otherAmerican college of rheumatologyes_ES
dc.subject.otherNetwork meta-analysises_ES
dc.subject.otherMeta-regressiones_ES
dc.titleCompared efficacy of rituximab, abatacept, and tocilizumab in patients with rheumatoid arthritis refractory to methotrexate or TNF inhibitors agents: a systematic review and network meta-analysises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1186/s42358-023-00298-zes_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International