TY - JOUR
T1 - Recent advances in the treatment strategy for AAV improved outcomes with intensive GC tapering
AU - Ono, Nobuyuki
AU - Kai, Tatsuya
AU - Takeyama, Yukiko
AU - Inoue, Yasushi
AU - Ueda, Naoyasu
AU - Nagano, Shuji
AU - Ohta, Shunichiro
AU - Inoue, Hisako
AU - Sawabe, Takuya
AU - Chifu, Yutaka
AU - Yoshizawa, Seiji
AU - Oryoji, Kensuke
AU - Kimoto, Yasutaka
AU - Miyake, Katsuhisa
AU - Ayano, Masahiro
AU - Mitoma, Hiroki
AU - Arinobu, Yojiro
AU - Miyamura, Tomoya
AU - Horiuchi, Takahiko
AU - Akashi, Koichi
AU - Tada, Yoshifumi
AU - Niiro, Hiroaki
N1 - Publisher Copyright:
© 2023 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.
PY - 2024/1
Y1 - 2024/1
N2 - Objective: To evaluate trends in results of care and management for antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV). Methods: We employed multicenter cohort data collected during 2011–2021, recruiting 43 patients with granulomatosis with polyangiitis (GPA) and 91 with microscopic polyangiitis (MPA). According to the median registration date of September 2015, patients have split into two groups: an early group and a late group (both of them, n = 67). To prevent bias, a propensity score according to numerous baseline characteristics variables was calculated; 50 matching members of each group were statistically extracted. Their treatments and clinical outcomes were examined at 6, 12, and 24 months after initial remission therapy. Results: Statistics demonstrated that the baseline characteristics were similar. The late group used rituximab (RTX) more often for both remission induction and maintenance therapy, compared with the early group. The mean daily PSL doses of the late group were significantly lower than those of early group at each time point. The late group discontinued PSL 14.0% at 12 months and 23.3% at 24 months. Despite their intensive glucocorticoids (GC) tapering, the remission rates and the relapse rates were significantly fairer in the late group. The Vasculitis Damage Index (VDI) and VDI due to GC at each time point were lower in the late group, and those differences had become wider over time. Conclusion: Recent developments in AAV treatment have allowed efficient remission and prevention of relapses, which in turn enabled extensive GC tapering causing fewer sequelae.
AB - Objective: To evaluate trends in results of care and management for antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV). Methods: We employed multicenter cohort data collected during 2011–2021, recruiting 43 patients with granulomatosis with polyangiitis (GPA) and 91 with microscopic polyangiitis (MPA). According to the median registration date of September 2015, patients have split into two groups: an early group and a late group (both of them, n = 67). To prevent bias, a propensity score according to numerous baseline characteristics variables was calculated; 50 matching members of each group were statistically extracted. Their treatments and clinical outcomes were examined at 6, 12, and 24 months after initial remission therapy. Results: Statistics demonstrated that the baseline characteristics were similar. The late group used rituximab (RTX) more often for both remission induction and maintenance therapy, compared with the early group. The mean daily PSL doses of the late group were significantly lower than those of early group at each time point. The late group discontinued PSL 14.0% at 12 months and 23.3% at 24 months. Despite their intensive glucocorticoids (GC) tapering, the remission rates and the relapse rates were significantly fairer in the late group. The Vasculitis Damage Index (VDI) and VDI due to GC at each time point were lower in the late group, and those differences had become wider over time. Conclusion: Recent developments in AAV treatment have allowed efficient remission and prevention of relapses, which in turn enabled extensive GC tapering causing fewer sequelae.
KW - ANCA
KW - ANCA-associated vasculitis
KW - glucocorticoid
KW - rituximab
KW - vasculitis
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U2 - 10.1111/1756-185X.15009
DO - 10.1111/1756-185X.15009
M3 - Article
C2 - 38129977
AN - SCOPUS:85180226733
SN - 1756-1841
VL - 27
JO - International Journal of Rheumatic Diseases
JF - International Journal of Rheumatic Diseases
IS - 1
M1 - e15009
ER -