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Effectiveness and safety of rituximab in severely relapsed antineutrophil cytoplasmic antibody–associated vasculitis: a retrospective analysis of a Japanese multicentre cohort from the J-CANVAS

  • Genki Kidoguchi,
  • Yusuke Yoshida,
  • Hirofumi Watanabe,
  • Tomohiro Sugimoto,
  • Sho Mokuda,
  • Takashi Kida,
  • Nobuyuki Yajima,
  • Satoshi Omura,
  • Daiki Nakagomi,
  • Yoshiyuki Abe,
  • Masatoshi Kadoya,
  • Naoho Takizawa,
  • Atsushi Nomura,
  • Yuji Kukida,
  • Naoya Kondo,
  • Yasuhiko Yamano,
  • Takuya Yanagida,
  • Koji Endo,
  • Kiyoshi Matsui,
  • Tohru Takeuchi,
  • Kunihiro Ichinose,
  • Masaru Kato,
  • Ryo Yanai,
  • Yusuke Matsuo,
  • Yasuhiro Shimojima,
  • Ryo Nishioka,
  • Ryota Okazaki,
  • Tomoaki Takata,
  • Takafumi Ito,
  • Mayuko Moriyama,
  • Ayuko Takatani,
  • Yoshia Miyawaki,
  • Toshiko Ito-Ihara,
  • Takashi Kawaguchi,
  • Yutaka Kawahito,
  • Shintaro Hirata

摘要

We aimed to clarify the long-term safety and efficacy of rituximab (RTX) as a remission induction therapy following severe relapse in patients with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV). We retrospectively collected the data of patients with severely relapsed AAV from a Japanese multicentre cohort. The primary exposure was RTX use; the primary outcome was complete remission (CR) proportions at week 24. Baseline characteristics were compared between the RTX and non-RTX groups. We performed multivariate logistic regression analysis and one-to-one propensity score matching analysis as a sensitivity analysis. Totally, 100 patients were enrolled: 52 in the RTX group and 48 in the non-RTX group. Baseline characteristics were comparable between the two groups, except for age, AAV subtype and ANCA serotype. The median age was 71 vs. 75 years, and the PR3-ANCA positivity rate was 44.2% vs. 18.8% in the RTX and non-RTX groups, respectively. No significant difference was observed in CR proportions at week 24 between the two groups (79.2% vs. 68.1%, p = 0.321), with an adjusted odds ratio of 1.27 (95% confidence interval [CI] 0.47–3.51). At week 48, CR proportions were significantly higher in the RTX group (91.7% vs. 64.9%, p = 0.005), with an adjusted odds ratio of 2.95 (95% CI 0.97–9.91). Serious infection rates were lower in the RTX group than in the non-RTX group, with no statistically significant difference. RTX was not superior to conventional immunosuppressive therapies at week 24 but showed significantly favourable results at week 48 for severely relapsed AAV.