Vcy. Ho et al., Intermittent short courses of cyclosporine microemulsion for the long-termmanagement of psoriasis: A 2-year cohort study, J AM ACAD D, 44(4), 2001, pp. 643-651
Background: Cyclosporine is effective in psoriasis, but long-term continuou
s therapy may be limited by renal impairment and hypertension. Intermittent
short courses of treatment should minimize side effects and improve the ri
sk-benefit ratio.
Objective: Our purpose was to assess the long-term efficacy and safety of i
ntermittent short courses of the microemulsion formulation of cyclosporine
(Neoral) in the management of chronic plaque psoriasis unresponsive to topi
cal therapies.
Methods: In a multicenter open cohort study, 76 subjects were treated inter
mittently over a 2-year period. Patients with chronic plaque psoriasis were
treated with cyclosporine until clearance of psoriasis or for a maximum of
12 weeks. Patients were then randomized into two groups. Group A stopped c
yclosporine abruptly, whereas group B had the dose reduced by 1 mg/kg per d
ay each week until cessation, which was within 4 weeks. On relapsing, patie
nts received further courses of cyclosporine. intermittent treatment was co
ntinued in this way for 2 years.
Results: There was no statistically significant difference in the percentag
e of time in remission during the 2-year period between patients randomized
to stop cyclosporine abruptly (56.2%) and patients randomized to taper cyc
losporine within 4 weeks (61.8%). The mean percentage of time that patients
received treatment during the study was 40.5% for randomization group A, 4
6.2% for randomization group B, and 42.8% overall. The median time to relap
se was 115.5 days after the first treatment course but became progressively
shorter after multiple treatment courses. Mean blood pressure and serum cr
eatinine levels did not show any clinically significant changes over time.
Conclusions: This study indicates that intermittent short courses of cylclo
sporine are effective in patients with moderate to severe psoriasis for up
to 2 years while improving the safety profile relative to continuous cyclos
porine monotherapy.