前往化源商城

Annals of the Rheumatic Diseases 2014-07-01

Randomised comparison of initial triple DMARD therapy with methotrexate monotherapy in combination with low-dose glucocorticoid bridging therapy; 1-year data of the tREACH trial.

P H de Jong, J M Hazes, H K Han, M Huisman, D van Zeben, P A van der Lubbe, A H Gerards, B van Schaeybroeck, P B de Sonnaville, M V van Krugten, J J Luime, A E Weel

文献索引:Ann. Rheum. Dis. 73(7) , 1331-9, (2014)

全文:HTML全文

摘要

To compare 1-year clinical efficacy of (1) initial triple disease-modifying antirheumatic drug therapy (iTDT) with initial methotrexate (MTX) monotherapy (iMM) and (2) different glucocorticoid (GC) bridging therapies: oral versus a single intramuscular injection in early rheumatoid arthritis.In a single-blinded randomised clinical trial patients were randomised into three arms: (A) iTDT (methotrexate+sulfasalazine+hydroxychloroquine) with GCs intramuscularly; (B) iTDT with an oral GC tapering scheme and (C) MTX with oral GCs similar to B. Primary outcomes were (1) area under the curve (AUC) of Health Assessment Questionnaire (HAQ) and Disease Activity Score (DAS) and (2) the proportion of patients with radiographic progression.281 patients were randomly assigned to arms A (n=91), B (n=93) or C (n=97). The AUC DAS and HAQ were respectively -2.39 (95% CI -4.77 to -0.00) and -1.67 (95% CI -3.35 to 0.02) lower in patients receiving iTDT than in those receiving iMM. After 3 months, treatment failure occurred less often in the iTDT group, resulting in 40% fewer treatment intensifications. The difference in treatment intensifications between the arms required to maintain the predefined treatment goal remained over time. No differences were seen between the two GC bridging therapies. Respectively 21%, 24% and 23% of patients in arms A, B and C had radiographic progression after 1 year. Patients receiving iTDT had more adjustments of their medication owing to adverse events than those receiving iMM.Treatment goals are attained more quickly and maintained with fewer treatment intensifications with iTDT than with iMM. However, no difference in radiographic progression is seen. Both GC bridging therapies are equally effective and, therefore, both can be used.ISRCTN26791028.Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

相关化合物

结构式 名称/CAS号 全部文献
二水合氨甲嘌呤 结构式 二水合氨甲嘌呤
CAS:133073-73-1
柳氮磺胺吡啶 结构式 柳氮磺胺吡啶
CAS:599-79-1
甲氨蝶呤 结构式 甲氨蝶呤
CAS:59-05-2
硫酸羟基氯喹 结构式 硫酸羟基氯喹
CAS:747-36-4