Journal article
Comparison of auranofin, methotrexate, and the combination of both in the treatment of rheumatoid arthritis : a controlled clinical trial
Arthritis and rheumatism, Vol.35(3), pp.259-269
1992
DOI: 10.1002/art.1780350304
PMID: 1536666
Abstract
Objective. To compare the relative safety and efficacy of auranofin (AUR), metbotrexate (MTX), and the combination of both in the treatment of active rheumatoid arthritis (RA).
Methods. Three hundred thirty-five patients with active RA were entered into a 48-week, prospective, controlled, double-blind, multicenter trial and were randomly assigned to 1 of 3 treatment groups.
Results. Two hundred eleven patients completed the trial. No remissions were seen, and there were no statistically significant differences among the treatment groups in the clinical or laboratory variables measured. Patients taking AUR alone had a slower onset of response than did patients taking MTX alone or in combination. Withdrawals because of adverse drug reactions were slightly more common for those taking combination therapy, but the differences were not statistically significant. Withdrawals because of lack of response were more common for single-drug therapy, with the difference between AUR and the combination reaching statistical significance. No unexpected adverse drug effects were identified, and all reactions resolved without sequelae.
Conclusion. Except for fewer withdrawals because of lack of response, combination therapy did not demonstrate any advantage in efficacy over single-drug treatment within the time frame of the study.
Details
- Title: Subtitle
- Comparison of auranofin, methotrexate, and the combination of both in the treatment of rheumatoid arthritis : a controlled clinical trial
- Creators
- H. James Williams - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesJohn R Ward - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesJames C Reading - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesRaye H Brooks - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesDaniel O Clegg - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesJohn L Skosey - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesMichael H Weisman - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesRobert F Willkens - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesJoyce Z Singer - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesGraciela S Alarcon - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesElizabeth H Field - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesPhilip J Clements - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesI Jon Russell - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesRodney F Hochman - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesDimitrios T Boumpas - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United StatesDwight A Marble - Univ. Utah school medicine, cooperative systematic studies rheumatic diseases program, Salt Lake City UT 84132, United States
- Resource Type
- Journal article
- Publication Details
- Arthritis and rheumatism, Vol.35(3), pp.259-269
- DOI
- 10.1002/art.1780350304
- PMID
- 1536666
- NLM abbreviation
- Arthritis Rheum
- ISSN
- 0004-3591
- eISSN
- 1529-0131
- Publisher
- Wiley
- Language
- English
- Date published
- 1992
- Academic Unit
- Immunology; Internal Medicine
- Record Identifier
- 9984094497102771
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