THE USE OF SANDIMMUN(R) (CYCLOSPORINE-A) IN SEVERE REFRACTORY RHEUMATOID-ARTHRITIS - THE BELGIAN EXPERIENCE

Citation
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
Citations number
NO
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
07703198
Volume
14
Year of publication
1995
Supplement
2
Pages
26 - 32
Database
ISI
SICI code
0770-3198(1995)14:<26:TUOS(I>2.0.ZU;2-9
Abstract
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.