ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2844

Predictive Factors for Mortality in Anti-melanoma-associated Gene 5 Antibody-associated Interstitial Lung Disease

Takahisa Gono1, Kenichi Masui 2, Naoshi Nishina 3, Shinji Sato 4 and Masataka Kuwana 5, 1Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, Tokyo, Japan, 2Department of Anaesthesiology, Show University School of Medicine, Saitama, Japan, 3Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 4Division of Rheumatology, Department of Internal Medicine, Tokai University School of Medicine, Yokohama, Japan, 5Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, Bunkyo-ku, Tokyo, Japan

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: interstitial lung disease and prognostic factors, Myositis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, November 12, 2019

Title: 5T113: Muscle Biology, Myositis & Myopathies II (2840–2845)

Session Type: ACR Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose: Anti-melanoma differentiation-associated gene 5 (MDA5) antibody is useful to predict mortality in patients with myositis–associated interstitial lung disease (ILD) because of high prevalence of rapidly progressive ILD, which is often refractory to conventional immunosuppressive treatment. In Japan, an intensive combination therapy consisting of corticosteroids (CS), calcineurin inhibitor, and intravenous cyclophosphamide, named the triple combo therapy, is widely used in patients with anti-MDA5-associated ILD anecdotally without evidence. A number of reports have shown that a group of anti-MDA5-associated ILD patients poorly respond to triple combo therapy. The aim of this study is to identify baseline characteristics that predict a poor response to triple combo therapy in patients with anti-MDA5-associated ILD, using a multicenter retrospective/prospective cohort JAMI, involving 497 incident cases of adult myositis-ILD.

Methods: We selected 212 patients with anti-MDA5 from the JAMI database. First, baseline characteristics and treatment regimens were compared between survivors and non-survivors to identify factors associated with mortality using univariate analysis. We then conducted a multivariate logistic regression analysis to identify independent risk factors for mortality with stepwise selection method, in which explanatory variables were selected using backward deletion (P ≥ 0.15) and forward inclusion (P < 0.1). A stratification tree model was constructed based on the combination of risk factors. Finally, we compared survival rates between patients treated with initial triple combo therapy and those without, by selecting patients randomly using JMP®13 software (SAS Institute Inc., Cary, NC, USA) by matching the baseline risk stratification and additional treatment regimen such as CS pulse therapy. Cumulative survival rates were compared using log-rank test.

Results: Mean age at disease onset was 55, 136 (64%) were female, and median disease duration at entry was 2 months. 73 patients died due to respiratory insufficiency at median of one month after treatment introduction. Independent risk factors for mortality were older age (odds ratio [OR] 1.07, 95% confidence interval [CI] 1.04-1.12, P < 0.0001), and lower SpO2/FiO2 ratio (OR 0.98, 95%CI 0.96-0.99, P < 0.0001). Cut-off values that best discriminate survivors and non-survivors identified using ROC curve analysis included age of 57 years and SpO2/FiO2 ratio of 450. We successfully generated a stratification tree model for mortality (Figure 1). Patients older than 57 years with SpO2/FiO2 ratio < 450 at diagnosis had the worst outcome with mortality rate of 76%. Cumulative survival rates were comparable between patients treated with initial triple combo therapy and those without even after matching the baseline risk stratification and additional treatment regimen (Figure 2).

Conclusion: Age and SpO2/FiO2 ratio at diagnosis are independent predictors for mortality in patients with anti-MDA5-associated ILD. We failed to demonstrate superiority of triple combo therapy over conventional therapy even adjusting baseline risk factors, suggesting urgent need of other therapeutic regimen for this devastating condition.

Figure 1

Figure 2


Disclosure: T. Gono, Astellas, 8, Astellas Pharma, 8, Boehringer-ingelheim Pharma, 8, Chugai, 8, Janssen, 8, MBL, 8, MEDICAL & BIOLOGICAL LABORATORIES CO., LTD, 8, Ono, 8, Ono Pharma, 8, Tanabe-Mitsubishi, 8, UCB Japan, 8; K. Masui, None; N. Nishina, None; S. Sato, MBL, 7, MEDICAL & BIOLOGICAL LABORATORIES CO., LTD, 7; M. Kuwana, Abbvie, 2, 8, Actelion, 2, 8, Actelion Pharmaceuticals, 2, 8, Astellas, 2, 8, Bayer, 5, Boehringer Ingelheim, 5, Boehringer-Ingelheim, 5, Chugai, 2, 5, 8, Corbus, 5, CSL Behring, 5, CSL Berling, 5, Eisai, 2, 8, Eli Lilly, 2, Janssen, 8, Japan Blood Products Organization, 8, MBL, 7, 8, Ono, 2, 8, Pfizer, 2, Reata, 5, Tanabe-Mitsubishi, 2, 8.

To cite this abstract in AMA style:

Gono T, Masui K, Nishina N, Sato S, Kuwana M. Predictive Factors for Mortality in Anti-melanoma-associated Gene 5 Antibody-associated Interstitial Lung Disease [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/predictive-factors-for-mortality-in-anti-melanoma-associated-gene-5-antibody-associated-interstitial-lung-disease/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2019 ACR/ARP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/predictive-factors-for-mortality-in-anti-melanoma-associated-gene-5-antibody-associated-interstitial-lung-disease/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology