Mg. Malaise et al., THE USE OF SANDIMMUN(R) (CYCLOSPORINE-A) IN SEVERE REFRACTORY RHEUMATOID-ARTHRITIS - THE BELGIAN EXPERIENCE, Clinical rheumatology, 14, 1995, pp. 26-32
Objective: To investigate practicability, efficacy and tolerability of
low starting doses of Sandimmun(R) (cyclosporin A) (2.5 mg/kg daily)
in patients with severe refractory rheumatoid arthritis in the short (
6 months) and middle (12 months) term. Methods: Fifty-nine patients, p
resenting with active and severe rheumatoid arthritis unresponding to
conventional DMARDs were allowed to start Sandimmun(R) at the dose of
2.5 mg/kg daily. This dose was progressively increased by steps of 25
mg daily up to a maximum of 5 mg/kg daily according to the renal funct
ion and blood pressure. Results: A mean maintenance dose of 3.9 mg/kg
daily was reached after 5 months and maintained throughout the study.
Twenty-one patients (36%) completed the one year study, The reasons fo
r discontinuation were: inefficacy (13), adverse events (17), both ine
fficacy and adverse events (5) and non-compliance (3). For those patie
nts who completed the trial, clinical relevant improvements were obser
ved within 3 months of treatment and were maintained until the end of
the study for the Lee functional and the Ritchie articular index, as w
ell as for the number of tender and swollen joints, No changes for the
grip strength, the biological and immunological parameters were obser
ved. Mean serum creatinine values rose from 0.81 mg/dl at start to 1.1
mg/dl after 5 months of therapy and remained at that level throughout
the study, In patients who discontinued, the serum creatinine level n
early normalized after one month of Sandimmun'' withdrawal. One hundre
d and sixty-two side effects were reported of which most were minor an
d known to occur with Sandimmun(R). Twenty-two cases (37% of patients)
dropped out for adverse events before 1 year treatment, The criteria
to withdraw the patients from the study differed greatly from centre t
o centre. Conclusions: Managing RA patients presenting with very long
and severe disease remains difficult, Therefore low dose Sandimmun(R)
(2.5-5 mg/kg daily) appears to be a valuable therapeutic opportunity i
n RA patients refractory to various other conventional drugs, includin
g methotrexate.