Certolizumab pegol, abatacept, tocilizumab or active conventional treatment in early rheumatoid arthritis: 48-week clinical and radiographic results of the investigator-initiated randomised controlled NORD-STAR trial
dc.contributor.author | Østergaard, Mikkel | |
dc.contributor.author | Van Vollenhoven, Ronald F | |
dc.contributor.author | Rudin, Anna | |
dc.contributor.author | Hetland, Merete Lund | |
dc.contributor.author | Schrumpf, Marte | |
dc.contributor.author | Nordström, Dan C | |
dc.contributor.author | Nurmohamed, Michael T | |
dc.contributor.author | Gudbjornsson, Bjorn | |
dc.contributor.author | Ørnbjerg, Lykke Midtbøll | |
dc.contributor.author | Bøyesen, Pernille | |
dc.contributor.author | Lend, Kristina | |
dc.contributor.author | Hørslev-Petersen, Kim | |
dc.contributor.author | Uhlig, Till | |
dc.contributor.author | Sokka, Tuulikki | |
dc.contributor.author | Grondal, Gerdur | |
dc.contributor.author | Krabbe, Simon | |
dc.contributor.author | Lindqvist, Joakim | |
dc.contributor.author | Gjertsson, Inger | |
dc.contributor.author | Glinatsi, Daniel | |
dc.contributor.author | Kapetanovic, Meliha Crnkic | |
dc.contributor.author | Aga, Anna-Birgitte | |
dc.contributor.author | Faustini, Francesca | |
dc.contributor.author | Parmanne, Pinja | |
dc.contributor.author | Lorenzen, Tove | |
dc.contributor.author | Giovanni, Cagnotto | |
dc.contributor.author | Back, Johan | |
dc.contributor.author | Hendricks, Oliver | |
dc.contributor.author | Vedder, Daisy | |
dc.contributor.author | Rannio, Tuomas | |
dc.contributor.author | Grenholm, Emma | |
dc.contributor.author | Ljoså, Maud-Kristine Aga | |
dc.contributor.author | Brodin, Eli | |
dc.contributor.author | Lindegaard, Hanne | |
dc.contributor.author | Söderbergh, Annika | |
dc.contributor.author | Rizk, Milad | |
dc.contributor.author | Kastbom, Alf | |
dc.contributor.author | Larsson, Per | |
dc.contributor.author | Uhrenholt, Line | |
dc.contributor.author | Just, Søren Andreas | |
dc.contributor.author | Stevens, David John | |
dc.contributor.author | Bay Laurbjerg, Trine | |
dc.contributor.author | Bakland, Gunnstein | |
dc.contributor.author | Olsen, Inge Christoffer | |
dc.contributor.author | Haavardsholm, Espen A. | |
dc.contributor.author | Lampa, Jon | |
dc.date.accessioned | 2024-02-05T09:43:46Z | |
dc.date.available | 2024-02-05T09:43:46Z | |
dc.date.issued | 2023-07-09 | |
dc.description.abstract | Background - The optimal first-line treatment in early rheumatoid arthritis (RA) is debated. We compared clinical and radiographic outcomes of active conventional therapy with each of three biological treatments with different modes of action.<p> <p>Methods - Investigator-initiated, randomised, blinded-assessor study. Patients with treatment-naïve early RA with moderate–severe disease activity were randomised 1:1:1:1 to methotrexate combined with (1) active conventional therapy: oral prednisolone (tapered quickly, discontinued at week 36) or sulfasalazine, hydroxychloroquine and intra-articular glucocorticoid injections in swollen joints; (2) certolizumab pegol; (3) abatacept or (4) tocilizumab. Coprimary endpoints were week 48 Clinical Disease Activity Index (CDAI) remission (CDAI ≤2.8) and change in radiographic van der Heijde-modified Sharp Score, estimated using logistic regression and analysis of covariance, adjusted for sex, anticitrullinated protein antibody status and country. Bonferroni’s and Dunnet’s procedures adjusted for multiple testing (significance level: 0.025).<p> <p>Results - Eight hundred and twelve patients were randomised. Adjusted CDAI remission rates at week 48 were: 59.3% (abatacept), 52.3% (certolizumab), 51.9% (tocilizumab) and 39.2% (active conventional therapy). Compared with active conventional therapy, CDAI remission rates were significantly higher for abatacept (adjusted difference +20.1%, p<0.001) and certolizumab (+13.1%, p=0.021), but not for tocilizumab (+12.7%, p=0.030). Key secondary clinical outcomes were consistently better in biological groups. Radiographic progression was low, without group differences.<p> <p>The proportions of patients with serious adverse events were abatacept, 8.3%; certolizumab, 12.4%; tocilizumab, 9.2%; and active conventional therapy, 10.7%.<p> <p>Conclusions - Compared with active conventional therapy, clinical remission rates were superior for abatacept and certolizumab pegol, but not for tocilizumab. Radiographic progression was low and similar between treatments. | en_US |
dc.identifier.citation | Østergaard, Van Vollenhoven, Rudin, Hetland, Schrumpf, Nordström, Nurmohamed, Gudbjornsson, Ørnbjerg, Bøyesen, Lend, Hørslev-Petersen, Uhlig, Sokka, Grondal, Krabbe, Lindqvist, Gjertsson, Glinatsi, Kapetanovic, Aga, Faustini, Parmanne, Lorenzen, Giovanni, Back, Hendricks, Vedder, Rannio, Grenholm, Ljoså, Brodin, Lindegaard, Söderbergh, Rizk, Kastbom, Larsson, Uhrenholt, Just, Stevens, Bay Laurbjerg, Bakland, Olsen, Haavardsholm, Lampa. Certolizumab pegol, abatacept, tocilizumab or active conventional treatment in early rheumatoid arthritis: 48-week clinical and radiographic results of the investigator-initiated randomised controlled NORD-STAR trial. Annals of the Rheumatic Diseases. 2023 | en_US |
dc.identifier.cristinID | FRIDAID 2176566 | |
dc.identifier.doi | 10.1136/ard-2023-224116 | |
dc.identifier.issn | 0003-4967 | |
dc.identifier.issn | 1468-2060 | |
dc.identifier.uri | https://hdl.handle.net/10037/32840 | |
dc.language.iso | eng | en_US |
dc.publisher | BMJ Publishing Group | en_US |
dc.relation.journal | Annals of the Rheumatic Diseases | |
dc.relation.projectID | Norges forskningsråd: 328657 | en_US |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2023 The Author(s) | en_US |
dc.title | Certolizumab pegol, abatacept, tocilizumab or active conventional treatment in early rheumatoid arthritis: 48-week clinical and radiographic results of the investigator-initiated randomised controlled NORD-STAR trial | en_US |
dc.type.version | acceptedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |