E. Reinholdkeller et al., RESPONSE TO TRIMETHOPRIM-SULFAMETHOXAZOLE IN WEGENERS GRANULOMATOSIS DEPENDS ON THE PHASE OF DISEASE, Quarterly Journal of Medicine, 89(1), 1996, pp. 15-23
We prospectively studied trimethoprim/sulfamethoxazole (T/S) in induci
ng remission in 'initial phase' Wegener's granulomatosis (WG), and in
sustaining remission in generalized WC, in 72 patients in various dise
ase stages. Nineteen patients with initial phase WG received T/S (2 x
960 mg/day). Another 24 patients with generalized WC received the same
dose of T/S (group A) and were compared with 21 patients receiving no
further treatment after standard therapy (group B). Eight patients we
re given T/S plus low-dose prednisone (group C). Eleven of 19 patients
(58%) with initial phase WC achieved complete or partial remission la
sting a median 43 months (range 6-88 months). Of the remaining eight (
42%), five showed local disease progression, and three developed gener
alized WG. In group A (T/S alone, generalized WC), 10/24 (42%) suffere
d a relapse after a median 13 months (range 4-58 months). In group B (
generalized WC, no further treatment) 29% of patients relapsed after a
median 22.5 months (range 18-26 months). All eight patients treated w
ith T/S plus low-dose prednisone (group C) suffered serious relapse af
ter 2-24 months. T/S induced long-term remission in > 50% of patients
with initial phase WG; however, neither T/S alone nor T/S plus low-dos
e prednisone sustained remission in generalized WG.