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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

医学 阿巴塔克普 托珠单抗 妥珠单抗 内科学 类风湿性关节炎 Golimumab公司 不利影响 外科 阿达木单抗 美罗华 淋巴瘤
作者
Mikkel Østergaard,Ronald van Vollenhoven,Anna Rudin,Merete Lund Hetland,Marte Schrumpf Heiberg,Dan Nordström,Michael T. Nurmohamed,Björn Guðbjörnsson,Lykke Midtbøll Ørnbjerg,Pernille Bøyesen,Kristina Lend,Kim Hørslev‐Petersen,Till Uhlig,Tuulikki Sokka,Gerður Gröndal,Simon Krabbe,Joakim Lindqvist,Inger Gjertsson,Daniel Glinatsi,Meliha C Kapetanovic
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:82 (10): 1286-1295 被引量:21
标识
DOI:10.1136/ard-2023-224116
摘要

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.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).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.The proportions of patients with serious adverse events were abatacept, 8.3%; certolizumab, 12.4%; tocilizumab, 9.2%; and active conventional therapy, 10.7%.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.NCT01491815.
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