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
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.