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Therapies for active rheumatoid arthritis after methotrexate failure.

The New England journal of medicine (2013-06-13)
James R O'Dell, Ted R Mikuls, Thomas H Taylor, Vandana Ahluwalia, Mary Brophy, Stuart R Warren, Robert A Lew, Amy C Cannella, Gary Kunkel, Ciaran S Phibbs, Aslam H Anis, Sarah Leatherman, Edward Keystone
RESUMEN

Few blinded trials have compared conventional therapy consisting of a combination of disease-modifying antirheumatic drugs with biologic agents in patients with rheumatoid arthritis who have active disease despite treatment with methotrexate--a common scenario in the management of rheumatoid arthritis. We conducted a 48-week, double-blind, noninferiority trial in which we randomly assigned 353 participants with rheumatoid arthritis who had active disease despite methotrexate therapy to a triple regimen of disease-modifying antirheumatic drugs (methotrexate, sulfasalazine, and hydroxychloroquine) or etanercept plus methotrexate. Patients who did not have an improvement at 24 weeks according to a prespecified threshold were switched in a blinded fashion to the other therapy. The primary outcome was improvement in the Disease Activity Score for 28-joint counts (DAS28, with scores ranging from 2 to 10 and higher scores indicating more disease activity) at week 48. Both groups had significant improvement over the course of the first 24 weeks (P=0.001 for the comparison with baseline). A total of 27% of participants in each group required a switch in treatment at 24 weeks. Participants in both groups who switched therapies had improvement after switching (P<0.001), and the response after switching did not differ significantly between the two groups (P=0.08). The change between baseline and 48 weeks in the DAS28 was similar in the two groups (-2.1 with triple therapy and -2.3 with etanercept and methotrexate, P=0.26); triple therapy was noninferior to etanercept and methotrexate, since the 95% upper confidence limit of 0.41 for the difference in change in DAS28 was below the margin for noninferiority of 0.6 (P=0.002). There were no significant between-group differences in secondary outcomes, including radiographic progression, pain, and health-related quality of life, or in major adverse events associated with the medications. With respect to clinical benefit, triple therapy, with sulfasalazine and hydroxychloroquine added to methotrexate, was noninferior to etanercept plus methotrexate in patients with rheumatoid arthritis who had active disease despite methotrexate therapy. (Funded by the Cooperative Studies Program, Department of Veterans Affairs Office of Research and Development, and others; CSP 551 RACAT ClinicalTrials.gov number, NCT00405275.)

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Sigma-Aldrich
Metotrexato hydrate, ≥98% (HPLC), powder
Sigma-Aldrich
Metotrexato hydrate, powder, BioReagent, suitable for cell culture, ≥98% (HPLC)
Sigma-Aldrich
Sulfato de hidroxicloroquina, ≥98% (HPLC), powder
Sigma-Aldrich
Metotrexato hydrate, meets USP testing specifications
Sigma-Aldrich
Metotrexato hydrate, ≥99.0% (sum of enantiomers, HPLC)
Sigma-Aldrich
Sulfasalazine, 97.0-101.5%
Methotrexate, European Pharmacopoeia (EP) Reference Standard
Methotrexate for peak identification, European Pharmacopoeia (EP) Reference Standard