Abstract
BackgroundThe study was undertaken to assess the efficacy of methotrexate (MTX) monotherapy on the radiographic progression of individual rheumatoid arthritis (RA) patients, each of whom had received MTX monotherapy for 3 years with an option to change to biological disease-modifying anti-rheumatic drugs (bDMARDs). We also looked for predictors of radiographic non-progression in these patients.MethodsRheumatoid patients (n = 161) were prospectively followed for 3 years while receiving low-dose MTX monotherapy unless disease was otherwise active and/or adverse events appeared. Their disease activity and radiographic progression were evaluated with reference to disease activity score 28 (DAS28), modified health assessment of questionnaire (mHAQ) and other indices. The change in van der Heijde-modified total Sharp score per year (∆TSS) was assessed using probability plots, in which the patients were classified into the subgroups showing structural remission (REM; ∆TSS ≤0.5), radiographic progression (∆TSS >3) or rapid radiographic progression (RRP; ∆TSS >5).ResultsMTX monotherapy, continued until disease became active and/or adverse event appeared, was associated with a significant improvement (p <0.0001) in the DAS28-ESR (3) scores, % DAS28 remission, and mHAQ scores each year, from baseline to 3 years. The mHAQ remission rate (∆mHAQ <0.5) and Boolean remission were also improved from 16 to 60 % and 0.8 to 24.0 %, respectively. We found that the ratio of patients classified as REM increased yearly from 62/161 (38.5 %) to 69/137 (50.4 %), while those classified as ∆TSS >3 decreased from 55/161 (34.2 %) to 28/137 (20.4 %) and those in RRP decreased from 35/161 (21.7 %) to 15/137 (10.9 %). Receiver operating characteristic (ROC) curve analyses showed that serum matrix metalloproteinase-3 (MMP-3) <103.7 ng/ml at outset predicts a patient subgroup that exhibits no radiographic progression.ConclusionsHalf of rheumatoid patients treated with MTX monotherapy for 3 years exhibited structural remission, and this outcome can be predicted at the outset by lower serum MMP-3.Electronic supplementary materialThe online version of this article (doi:10.1186/s13075-016-0948-7) contains supplementary material, which is available to authorized users.
Highlights
The study was undertaken to assess the efficacy of methotrexate (MTX) monotherapy on the radiographic progression of individual rheumatoid arthritis (RA) patients, each of whom had received MTX monotherapy for 3 years with an option to change to biological disease-modifying anti-rheumatic drugs
O’Dell et al have shown that treating patients with MTX monotherapy initially, while later providing an option to step up to combination therapy produces outcomes similar to those seen with combination therapies consisting of cDMARDS and/or biological diseasemodifying anti-rheumatic drug (bDMARD) that are provided from the outset [19]
Disease activity was found to be significantly improved each year starting at baseline and continuing to 3 years: disease activity score 28 (DAS28)-erythrocyte sedimentation rate (ESR) (3) decreased from 5.2 ± 1.1 to 3.9 ± 1.4 (p
Summary
The study was undertaken to assess the efficacy of methotrexate (MTX) monotherapy on the radiographic progression of individual rheumatoid arthritis (RA) patients, each of whom had received MTX monotherapy for 3 years with an option to change to biological disease-modifying anti-rheumatic drugs (bDMARDs). Methotrexate (MTX) has been recommended as a first-line drug for the initial treatment of rheumatoid arthritis (RA), and as an essential component of combination therapies utilizing either conventional disease-modifying anti-rheumatic drugs (cDMARDs) or biological DMARDs (bDMARDs) [1, 2]. O’Dell et al have shown that treating patients with MTX monotherapy initially, while later providing an option to step up to combination therapy produces outcomes similar to those seen with combination therapies consisting of cDMARDS and/or bDMARDs that are provided from the outset [19].
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