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Optimal Dose of Intravenous Cyclophosphamide during remission induction therapy in ANCA-associated vasculitis: a retrospective cohort study of J-CANVAS.
Sofue, Hideaki; Kida, Takashi; Hirano, Aiko; Omura, Satoshi; Kadoya, Masatoshi; Nakagomi, Daiki; Abe, Yoshiyuki; Takizawa, Naoho; Nomura, Atsushi; Kukida, Yuji; Kondo, Naoya; Yamano, Yasuhiko; Yanagida, Takuya; Endo, Koji; Hirata, Shintaro; Matsui, Kiyoshi; Takeuchi, Tohru; Ichinose, Kunihiro; Kato, Masaru; Yanai, Ryo; Matsuo, Yusuke; Shimojima, Yasuhiro; Nishioka, Ryo; Okazaki, Ryota; Takata, Tomoaki; Ito, Takafumi; Moriyama, Mayuko; Takatani, Ayuko; Miyawaki, Yoshia; Ito-Ihara, Toshiko; Yajima, Nobuyuki; Kawaguchi, Takashi; Fujioka, Kazuki; Fujii, Wataru; Seno, Takahiro; Wada, Makoto; Kohno, Masataka; Kawahito, Yutaka.
Afiliação
  • Sofue H; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kida T; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Hirano A; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Omura S; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kadoya M; Center for Rheumatic Disease, Japanese Red Cross Society Kyoto Daiichi Hospital, Kyoto, Japan.
  • Nakagomi D; Department of Rheumatology, University of Yamanashi Hospital, Yamanashi, Japan.
  • Abe Y; Department of Internal Medicine and Rheumatology, Juntendo University, Tokyo, Japan.
  • Takizawa N; Department of Rheumatology, Chubu Rosai Hospital, Nagoya, Japan.
  • Nomura A; Immuno-Rheumatology Center, St. Luke's International Hospital, Tokyo, Japan.
  • Kukida Y; Department of Rheumatology, Japanese Red Cross Society Kyoto Daini Hospital, Kyoto, Japan.
  • Kondo N; Department of Nephrology, Kyoto Katsura Hospital, Kyoto, Japan.
  • Yamano Y; Department of Respiratory Medicine and Allergy, Tosei General Hospital, Aichi, Japan.
  • Yanagida T; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Endo K; Department of Hematology and Rheumatology, Kagoshima University Hospital, Kagoshima, Japan.
  • Hirata S; Department of General Internal Medicine, Tottori Prefectural Central Hospital, Tottori, Japan.
  • Matsui K; Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan.
  • Takeuchi T; Department of Diabetes, Endocrinology and Clinical Immunology, Hyogo Medical University School of Medicine, Hyogo, Japan.
  • Ichinose K; Department of Internal Medicine (IV), Osaka Medical and Pharmaceutical University, Osaka, Japan.
  • Kato M; Department of Immunology and Rheumatology, Division of Advanced Preventive Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Yanai R; Department of Rheumatology, Shimane University Faculty of Medicine, Shimane, Japan.
  • Matsuo Y; Department of Rheumatology, Endocrinology and Nephrology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Shimojima Y; Division of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
  • Nishioka R; Department of Rheumatology, Tokyo Kyosai Hospital, Tokyo, Japan.
  • Okazaki R; Department of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Takata T; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan.
  • Ito T; Department of Rheumatology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
  • Moriyama M; Division of Respiratory Medicine and Rheumatology, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan.
  • Takatani A; Division of Gastroenterology and Nephrology, Tottori University, Yonago, Japan.
  • Miyawaki Y; Division of Nephrology, Shimane University Hospital, Shimane, Japan.
  • Ito-Ihara T; Department of Rheumatology, Shimane University Faculty of Medicine, Shimane, Japan.
  • Yajima N; Rheumatic Disease Center, Sasebo Chuo Hospital, Nagasaki, Japan.
  • Kawaguchi T; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Fujioka K; The Clinical and Translational Research Center, University Hospital, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Fujii W; Division of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
  • Seno T; Department of Healthcare Epidemiology, Kyoto University Graduate School of Medicine and Public Health, Kyoto, Japan.
  • Wada M; Center for Innovative Research for Communities and Clinical Excellence, Fukushima Medical University, Fukushima, Japan.
  • Kohno M; Department of Practical Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
  • Kawahito Y; Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Mod Rheumatol ; 2023 Oct 06.
Article em En | MEDLINE | ID: mdl-37801552
ABSTRACT

OBJECTIVES:

To identify the optimal dose of intravenous cyclophosphamide (IVCY) for induction therapy for anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV).

METHODS:

We retrospectively assessed patients with AAV who received IVCY every 2-3 weeks during the remission induction phase. The associations of the IVCY dose with infection-free survival and relapse-free survival were analysed using a Cox regression model. We compared patients in three categories very low-dose (VLD), low-dose (LD), and conventional dose (CD) (<7.5 mg/kg, 7.5-12.5 mg/kg, and >12.5 mg/kg, respectively). The non-linear association between IVCY dose and the outcomes were also evaluated.

RESULTS:

Of the 80 patients (median age 72 years), 12, 42, and 26 underwent the VLD, LD, and CD regimens, respectively, of whom 4, 3, and 7 developed infection or died. The adjusted hazard ratios for infection or death were 4.3 (95% confidence interval (CI) 0.94-19.8) for VLD and 5.1 (95% CI 1.21-21.3) for CD, compared with LD. We found the hazard ratio for infection or death increased when the initial IVCY dose exceeded 9 mg/kg. Relapse-free survival did not differ clearly.

CONCLUSION:

Low-dose IVCY (7.5-12.5 mg/kg) may result in fewer infections and similar relapse rates compared with the conventional regimen (>12.5 mg/kg).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Revista: Mod Rheumatol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Revista: Mod Rheumatol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão