Abstract

BackgroundDetermining potential predictors of clinical response would allow a more personalized rheumatoid arthritis (RA) treatment approach in heterogeneous populations such as Latin American (LA) patients.MethodsPost hoc analysis to identify baseline characteristics predictive of clinical remission in response to treatment with etanercept (ETN) plus methotrexate (MTX) in LA patients with moderate to severe MTX-resistant RA. We report data from the group of patients who received ETN 50 mg/week plus MTX (ETN + MTX, n = 281) in a clinical trial consisting of an initial 24-week open-label phase, followed by a 104-week extension. Remission was defined as 28-joint Disease Activity Score with erythrocyte sedimentation rate (DAS28-ESR) score < 2.6. Cutoff values to dichotomize baseline variables maximizing the detection of remission were obtained from Receiver Operator Curve analyses. Baseline dichotomized and categorical variables were analyzed altogether in a stepwise logistic regression model. Odds of attaining response at Weeks 24 and 128 were estimated for each significant predictor.ResultsAt Week 24 and Week 128, 27% (66/241) and 42% (91/219) of patients in the ETN + MTX group achieved remission. On average, patients achieving remission were younger and had lower baseline ESR, lower Physician Global Assessment (PGA) scores, lower total Health Assessment Questionnaire (HAQ) scores, and lower visual analog scale (VAS) Pain scores compared with patients who did not achieve remission. The best subset of baseline variables predicting Week 24 remission in the stepwise regression model were age ≤ 49 years (odds ratio [OR] 2.93), body mass index (BMI) > 28.5 kg/m2 (OR 3.24), disease duration > 3.7 years (OR 2.22), ESR ≤ 42 mm/h (OR 2.72), PGA ≤ 6 (OR 3.21), tender joint count ≤ 14 (OR 2.25), and total HAQ score ≤ 1.6 (OR 2.86). At Week 128, age ≤ 42 years (OR 2.21), SF-36 Mental Health Scale score > 39.6 (OR 2.16), White race (OR 4.07), > 18 swollen joints (OR 2.11), and VAS Pain ≤ 41 (OR 6.05) at baseline were the best subset of significant predictors of remission.ConclusionsIn LA patients with RA, younger age, higher BMI, longer disease duration, higher SF-36 Mental Health Scale score, higher swollen joint count, and overall lower disease activity predicted clinical response to ETN + MTX therapy.Trial registration: ClinicalTrials.gov Identifier: NCT00848354.

Highlights

  • Determining potential predictors of clinical response would allow a more personalized rheumatoid arthritis (RA) treatment approach in heterogeneous populations such as Latin American (LA) patients

  • The population of Latin America is highly diverse and differs from Western populations in its racial, ethnic, and socio-economic make-up [5], factors that have been associated with the treatment outcomes of RA [6, 7]

  • During the open-label, 104-week extension phase, benefits of ETN plus MTX treatment were maintained for up to 2 years [9], and a post hoc analysis demonstrated that clinical outcomes at Week 12 could be used as predictors of patient-reported outcomes at Week 24 [10]

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Summary

Introduction

Determining potential predictors of clinical response would allow a more personalized rheumatoid arthritis (RA) treatment approach in heterogeneous populations such as Latin American (LA) patients. A majority of clinical trials investigating treatments for RA, including those of the tumor necrosis factor (TNF) inhibitor etanercept (ETN), have been conducted in patients from North America and Europe. In a 24-week, randomized open-label study of methotrexate (MTX)-resistant patients with moderate or severe RA, conducted in Latin America (NCT00848354), ETN plus MTX was shown to be superior to MTX plus another conventional disease-modifying antirheumatic drug (DMARD) [8]. During the open-label, 104-week extension phase, benefits of ETN plus MTX treatment were maintained for up to 2 years [9], and a post hoc analysis demonstrated that clinical outcomes at Week 12 could be used as predictors of patient-reported outcomes at Week 24 [10]

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