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Cited by 353

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Concomitant Leflunomide Therapy in Patients with Active Rheumatoid Arthritis despite Stable Doses of Methotrexate: A Randomized, Double-Blind, Placebo-Controlled Trial

Kremer, Joel M., Genovese, Mark C., Cannon, Grant W., Caldwell, Jacques R., Cush, John J., Furst, Daniel E., Luggen, Michael E., Keystone, Ed, Weisman, Michael H., Bensen, William M., Kaine, Jeffrey L., Ruderman, Eric M., Coleman, Patricia, Curtis, David L., Kopp, Elliot J., Kantor, Seth M., Waltuck, Jonathan, Lindsley, Herbert B., Markenson, Joseph A., Strand, Vibeke, Crawford, Bruce, Fernando, Indra, Simpson, Karen, Bathon, Joan M.·2002·Annals of Internal Medicine

Abstract

BACKGROUND: Disease-modifying antirheumatic drugs may confer greater benefits when combined with the antimetabolite methotrexate. OBJECTIVE: To evaluate the efficacy and safety of leflunomide versus placebo when added to ongoing, stable-dose methotrexate therapy in patients with persistently active rheumatoid arthritis. DESIGN: 24-week, multicenter, randomized, double-blind, placebo-controlled trial. SETTING: 20 centers in the United States and Canada. PATIENTS: Patients with persistent rheumatoid arthritis, as defined by American College of Rheumatology (ACR) criteria, despite receiving methotrexate for at least 6 months. INTERVENTION: Leflunomide or matching placebo added to existing methotrexate therapy. MEASUREMENTS: The primary efficacy variable was the rate of achievement of 20% improvement in ACR criteria (ACR20) at the end of the study. The Health Assessment Questionnaire Disability Index was assessed at each visit, and the Medical Outcomes Study 36-Item Short Form was completed as an end point analysis. RESULTS: In the leflunomide and placebo groups, 46.2% and 19.5% of patients, respectively, met ACR20 criteria at 24 weeks (P < 0.001). Clinical improvement was demonstrated by statistically significant mean changes in individual components of the ACR20 response criteria. Discontinuation rates were similar in both treatment groups (23.1% in the leflunomide group and 24.8% in the placebo group), as were the overall incidences of adverse events (89.2% vs. 89.5%, respectively). Adverse events were predominantly mild or moderate. CONCLUSIONS: Combination therapy with leflunomide and methotrexate provides statistically significant clinical benefit in patients with active rheumatoid arthritis who are receiving methotrexate therapy. Leflunomide plus methotrexate is generally well tolerated and can be used safely with appropriate liver enzyme and hematologic monitoring.

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Crossref · 10.7326/0003-4819-137-9-200211050-00007

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Metadata

Authors
Kremer, J. M., Genovese, M. C., Cannon, G. W., Caldwell, J. R., Cush, J. J., Furst, D. E., Luggen, M. E., Keystone, E., Weisman, M. H., Bensen, W. M., Kaine, J. L., Ruderman, E. M., Coleman, P., Curtis, D. L., Kopp, E. J., Kantor, S. M., Waltuck, J., Lindsley, H. B., Markenson, J. A., Strand, V., Crawford, B., Fernando, I., Simpson, K., & Bathon, J. M.
Venue
Annals of Internal Medicine
Published
2002-11-05
Volume
137
Issue
9
Pages
726-733
ISSN
  • 0003-4819 (ISSN-L)
  • 1539-3704
OpenAlex
W2100753300
Cited by
353
References
1
FWCI
16.17
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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