Rationale of concomitant cyclophosphamide for remission-induction in patients with antineutrophil cytoplasmic antibody-associated vasculitis: A propensity score-matched analysis of two nationwide prospective cohort studies.


Journal

Modern rheumatology
ISSN: 1439-7609
Titre abrégé: Mod Rheumatol
Pays: England
ID NLM: 100959226

Informations de publication

Date de publication:
Jan 2021
Historique:
pubmed: 21 12 2019
medline: 8 5 2021
entrez: 21 12 2019
Statut: ppublish

Résumé

We evaluated the effectiveness of cyclophosphamide for patients with microscopic polyangiitis and granulomatosis with polyangiitis. Patients treated with cyclophosphamide and glucocorticoid (cyclophosphamide group) or glucocorticoid alone (non-cyclophosphamide group) for remission-induction were enrolled from two Japanese nationwide prospective inception cohort studies. The effectiveness and safety outcomes were compared before and after propensity score (PS)- matching. Proportion of patients achieving Birmingham Vasculitis Activity Score (BVAS)-remission and BVAS-remission plus a daily prednisolone dosage of ≤10 mg (GC-remission) by Month 6 were not significantly different between cyclophosphamide and non-cyclophosphamide groups before ( Concomitant cyclophosphamide use may improve GC-remission by Month 6 in MPO-ANCA-positive patients and could exert glucocorticoid sparing effect.

Identifiants

pubmed: 31859544
doi: 10.1080/14397595.2019.1707997
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0
Glucocorticoids 0
Immunosuppressive Agents 0
Cyclophosphamide 8N3DW7272P
Prednisolone 9PHQ9Y1OLM
Peroxidase EC 1.11.1.7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

205-213

Auteurs

Haruki Watanabe (H)

Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Ken-Ei Sada (KE)

Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Yoshinori Matsumoto (Y)

Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Masayoshi Harigai (M)

Department of Rheumatology, School of Medicine, Tokyo Women's Medical University, Tokyo, Japan.

Koichi Amano (K)

Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.

Shouichi Fujimoto (S)

Department of Hemovascular Medicine and Artificial Organs, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

Hiroaki Dobashi (H)

Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine, Faculty of Medicine, Kagawa University, Miki-cho, Japan.

Yukio Yuzawa (Y)

Department of Nephrology, Fujita Health University School of Medicine, Toyoake, Japan.

Kunihiro Yamagata (K)

Department of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.

Eri Muso (E)

Department of Nephrology and Dialysis, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka, Japan.

Yoshihiro Arimura (Y)

Department of Nephrology and Rheumatology, Kyorin University School of Medicine, Tokyo, Japan.

Hirofumi Makino (H)

Okayama University, Okayama, Japan.

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Classifications MeSH