Rituximab therapy is more effective than cyclophosphamide therapy for Japanese patients with anti-topoisomerase I-positive systemic sclerosis-associated interstitial lung disease.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 02 06 2019
accepted: 15 08 2019
pubmed: 11 9 2019
medline: 14 4 2020
entrez: 11 9 2019
Statut: ppublish

Résumé

Systemic sclerosis-associated interstitial lung disease (SSc-ILD) is the most frequent cause of death for SSc but there is still no sufficient treatment available. Although cyclophosphamide (CYC) therapy is a common treatment which has shown statistical efficacy against SSc-ILD to date, its effects are temporary and not enough. Rituximab (RTX), the anti-CD20 monoclonal antibody, has recently shown efficacy in many autoimmune diseases. In SSc-ILD, RTX is also considered to be one of the novel treatment candidates. However, studies of SSc-ILD in Japanese treated with RTX have only a few case reports. Therefore, in this study, we retrospectively compared nine patients treated with RTX and 30 patients treated with CYC to investigate the efficacy of RTX treatment for Japanese anti-topoisomerase I-positive SSc-ILD patients. At the 24-month evaluation, the improvement rates of percent predicted of forced vital capacity and percent predicted of diffusing capacity of the lung carbon monoxide in the RTX-treated group were significantly higher than those in the CYC-treated group (20.6 ± 8.8% vs 1.1 ± 3.9%; P < 0.05 and 34.0 ± 6.0% vs -1.5 ± 2.8%; P < 0.01, respectively). In addition, skin thickness scores also showed a marked improvement from 13.5 points before the start of treatment to 5.8 points after 24 months by RTX therapy (P < 0.05). These results suggest that RTX treatment is more effective for Japanese SSc-ILD patients than CYC treatment. In the future, it is expected that large-scale clinical trials will show the usefulness of RTX treatment for SSc-ILD.

Identifiants

pubmed: 31502326
doi: 10.1111/1346-8138.15079
doi:

Substances chimiques

Immunosuppressive Agents 0
Rituximab 4F4X42SYQ6
Cyclophosphamide 8N3DW7272P
DNA Topoisomerases, Type I EC 5.99.1.2

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1006-1013

Informations de copyright

© 2019 Japanese Dermatological Association.

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Auteurs

Satoshi Ebata (S)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Ayumi Yoshizaki (A)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Takemichi Fukasawa (T)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Shunsuke Miura (S)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Takehiro Takahashi (T)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Hayakazu Sumida (H)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Yoshihide Asano (Y)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Shinichi Sato (S)

Department of Dermatology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

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