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Annals of the Rheumatic Diseases 2001;60:514-517; doi:10.1136/ard.60.5.514
Copyright © 2001 BMJ Publishing Group Ltd & European League Against Rheumatism.
Ann Rheum Dis 2001;60:514-517 ( May )

Concise report

Treatment with cyclosporin switching to hydroxychloroquine in patients with rheumatoid arthritis W-U Kima, Y-I Seoa, S-H Parka, W-K Leeb, S-K Leeb, S-I Paeka, C-S Choa, H-H Songc, H-Y Kima

a Centre for Rheumatic Disease, Kang-Nam St Mary's Hospital, School of Medicine, The Catholic University of Korea, Seoul, Republic of Korea, b Department of Rheumatology, Yonsei University College of Medicine, Seoul, Republic of Korea, c Department of Biostatistics, The Catholic University of Korea, Seoul, Republic of Korea

Correspondence to: Dr H-Y Kim, Division of Rheumatology, Department of Internal Medicine, School of Medicine, The Catholic University of Korea, Centre for Rheumatic Diseases in Kang-Nam St Mary's Hospital, 505 Banpo-Dong, Seocho-Ku, Seoul, 137-040, Korea rheuma{at}cmc.cuk.ac.kr

Accepted for publication 3 October 2000

OBJECTIVE---To investigate the therapeutic benefit of cyclosporin A (CSA) switching to hydroxychloroquine (HCQ) in patients with rheumatoid arthritis (RA).
METHODS---Thirty four patients with RA who displayed residual inflammation and disability despite partial responses to prior maximal tolerated doses of methotrexate, were included. All were treated with a staged approach using CSA for 24 weeks to induce clinical improvement, followed by HCQ for 16 weeks to maintain the improvement. Seven ACR core set measures were evaluated every four to eight weeks.
RESULTS---During a 40 week open trial, 27/34 patients completed the study. CSA treatment significantly reduced the tender joints score, swollen joints score, visual analogue pain scale, patient's or doctor's global assessment, patient's self assessed disability, and C reactive protein. Compared with the time of entry into the trial, patients who switched from CSA to HCQ still possessed significantly lower levels of most variables, determined at 28, 32, and 40 weeks. According to the ACR 20% improvement definition, 15/27 (56%) patients had improved at 24 weeks after CSA treatment, and 14/27 (52%) remained improved at 16 weeks after the change to HCQ. Frequent side effects, such as hypertrichosis, gastrointestinal trouble, and hypertension, were noted during CSA treatment, but most of these disappeared after switching to HCQ. The mean levels of blood pressure and serum creatinine were significantly increased during CSA treatment, but returned to normal after changing to HCQ.
CONCLUSIONS---The data suggest that CSA switching to HCQ treatment may be an effective strategy for patients with RA partially responding to methotrexate, particularly those with toxicity due to CSA.


© 2001 by Annals of the Rheumatic Diseases

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