Objective. To assess the tolerability of sulfasalazine in a clinic set
ting and determine its longterm effectiveness with respect to articula
r disease and prevention of radiographic progression in patients with
psoriatic arthritis (PsA). Methods. Patients who were given sulfasalaz
ine during their attendance at the University of Toronto Psoriatic Art
hritis Clinic were enrolled in the study. For patients that were able
to tolerate sulfasalazine for at least 3 months a matched control was
identified who did not receive sulfasalazine. The primary outcome meas
ures were the tolerability of sulfasalazine, clinical response of the
actively inflamed joints at 6 and 12 months, and the change in radiogr
aphic score at 24 months. Results. Thirty-six patients received sulfas
alazine. Fourteen of 16 patients discontinued sulfasalazine due to one
or more side effects occurring within 3 months of treatment initiatio
n. For the remaining 20 patients, a 50% reduction in actively inflamed
joint count was noted in 7/20 patients at 6 months and 11/15 patients
at 12 months, compared to 7/19 patients in the control group at 6 mon
ths and 10/20 patients at 12 months. The mean change in the radiograph
ic score at 24 months between the 2 groups was not statistically signi
ficant. Conclusion. Sulfasalazine was not well tolerated in patients w
ith PsA in our clinic. For those able to tolerate sulfasalazine, there
was no evidence of a treatment effect with respect to articular invol
vement. In addition, sulfasalazine does not appear to halt radiographi
c progression in PsA.