The aim of this study was to evaluate the efficacy of fludarabine treatment
in patients suffering from refractory rheumatoid arthritis. Four patients
affected by refractory seropositive rheumatoid arthritis underwent treatmen
t with fludarabine for 6 months. The drug was administered intravenously at
a dose of 25 mg the first month in a single infusion, and then monthly for
5 months at a dose of 25 mg for 3 consecutive days. All four patients obta
ined no clinical benefit from the treatment; moreover, inflammation indices
worsened and the prednisone dosage was increased during the trial, in spit
e of a significant fall in CD4+ T cells. In our experience low-dose fludara
bine is not useful in the treatment of refractory rheumatoid arthritis.