TOXICITY PROFILE OF DUAL METHOTREXATE COMBINATIONS WITH GOLD, HYDROXYCHLOROQUINE, SULFASALAZINE AND MINOCYCLINE IN RHEUMATOID-ARTHRITIS PATIENTS

Citation
O. Elkayam et al., TOXICITY PROFILE OF DUAL METHOTREXATE COMBINATIONS WITH GOLD, HYDROXYCHLOROQUINE, SULFASALAZINE AND MINOCYCLINE IN RHEUMATOID-ARTHRITIS PATIENTS, Rheumatology international, 17(2), 1997, pp. 49-53
Citations number
24
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
01728172
Volume
17
Issue
2
Year of publication
1997
Pages
49 - 53
Database
ISI
SICI code
0172-8172(1997)17:2<49:TPODMC>2.0.ZU;2-S
Abstract
The purpose of the present study was to evaluate the toxicity and tole rability of methotrexate (MTX)/ gold (G; group 1) combination therapy as compared to other MTX combinations [MTX with hydroxychloroquine (HC Q; group 2), MTX with sulphasalazine (SASP; group 3) and MTX with mino cycline (MNC; group 4)]. The hospital records of 127 consecutive rheum atoid arthritis (RA) patients who were treated with these combinations during a period of 24 months were retrospectively reviewed. The toxic ity and tolerability of the MTX/G combination was compared to the othe r dual MTX combinations and also to MTX alone using data previously re ported by us on 126 RA patients treated with single MTX therapy. The m ean exposure time to treatment was 16 months in group 1 and 13 months in the other dual MTX combinations. During the period of follow-up, th e combination was stopped in 22 out of 42 patients in group 1 (52%) in comparison with 54 patients out of 86 patients (63%) in the other dua l regimen groups. The discontinuation rate was highest in group 4 (due to side effects and lack of compliance) and this was statistically si gnificant in comparison with group 1. The proportion of adverse events was lowest in group 1 (14%) and highest in groups 3 and 4 (25%). Side effects were reversible and comparable with those of MTX alone (23%). No fatal or life-threatening side effects were recorded during any of these MTX combination therapies. We concluded that the combinations o f MTX with G, HCQ, SASP and MNC in RA were relatively well tolerated. No increase in toxicity compared with MTX alone was observed. The lowe st rate of side effects was noted in group 1, while group 4 presented the highest discontinuation rate.