Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

Malignancy Risk Varies with Treatment in Systemic Necrotizing Vasculitis

Reuters Staff  |  January 7, 2020

NEW YORK (Reuters Health)—The risk of malignancy in patients with systemic necrotizing vasculitis varies according to the treatment received, according to an analysis of five randomized controlled trials.

Previous studies reported an increased risk of malignancy in patients with systemic necrotizing vasculitis, and a more recent study from the European Vasculitis Study Group, based on data through 2007, found a smaller increased cancer risk magnitude compared with earlier studies.

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

For the current study, Dr. Antoine Lafarge from Cochin Hospital and National Referral Center for Rare Systemic Autoimmune Diseases, Paris, and colleagues in the French Vasculitis Study Group used data from 733 patients with systemic necrotizing vasculitis enrolled between 1993 and 2012 in one of five randomized controlled trials to evaluate the malignant burden of systemic necrotizing vasculitis.

During 4485.9 person-years of observation, 5.3% of patients developed malignancies (a rate of 869.5 cases per 100,000 person-years), including 4.6% with solid cancers (757.9 cases per 100,000 person-years) and 0.7% with hematological malignancies (111.5 per 100,000 person-years).

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

The calculated standardized incidence ratios for all cancers did not differ significantly between these patients and the general population included in the French National registry, according to the online report in Annals of the Rheumatic Diseases.1

In multivariate analyses, age at least 65 and use of azathioprine and methotrexate as maintenance were independently associated with the increased occurrence of malignancy.

When it occurred, malignancy was associated with poorer overall survival, and the cause of death was directly related to the malignancy or its treatment in all 19 patients with cancer who died.

“A key finding of our study was the lower incidence of malignancy than previously reported in patients with [systemic necrotizing vasculitis], which was now comparable to that of the general population,” the authors note. “This decreased risk of malignancy may be driven by the more extensive use of cyclophosphamide-sparing strategies.”

“Taken together,” they conclude, “these findings suggest that malignancy should no longer be considered as a predominant feature driving the therapeutic strategy.”

Dr. Lafarge and co-author Dr. Benjamin Terrier did not respond to a request for comments.


Reference

  1. Lafarge A, Joseph A, Pagnoux C, et al. Risk of malignancy in patients treated for systemic necrotising vasculitis. Ann Rheum Dis. 2019 Nov 25. pii: annrheumdis-2019-216452. [Epub ahead of print]

Share: 

Filed under:ConditionsVasculitis Tagged with:malignancysystemic necrotizing vasculitisVasculitis

Related Articles
    Valentyn Volkov / shutterstock.com

    Did Shiitake Mushrooms Induce Immune-Mediated Necrotizing Myopathy?

    April 15, 2019

    Idiopathic inflammatory myopathies are heterogenous, acquired immune-mediated muscle diseases. Over the past decade, immune-mediated necrotizing myopathy has been recognized as a subcategory of idiopathic inflammatory myopathy characterized by myofiber necrosis in the absence of prominent inflammatory cells.1 Autoantibodies against signal recognition particle (SRP) and 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) are thought to be associated with the…

    ilusmedical / shutterstock.com

    The State of Clinical Research in Vasculitis: 2021

    January 19, 2021

    It is an exciting time in the world of vasculitis research. More clinical studies and trials are being conducted now than at any time in history. In the past ten years, four drugs have been approved by the U.S. Food & Drug Administration (FDA) and other regulatory agencies specifically for the treatment of vasculitis: Rituximab…

    Fellows’ Forum Case Report: Necrotizing Autoimmune Myopathy

    December 18, 2017

    Necrotizing autoimmune myopathy (NAM) is a relatively recently discovered subgroup of inflammatory myopathies. NAM is characterized by predominant muscle fiber necrosis and regeneration with little or no inflammation.1 One subgroup of NAM is 3-hydroxy-3-methylglutaryl-CoA reductase antibody (HMGCR Ab)-related immune-mediated necrotizing myopathy (IMNM), which occurs (rarely) after statin exposure, with a rough incidence of two per…

    Meet the Challenge of Primary CNS Vasculitis

    September 1, 2011

    Diagnosis and treatment of this rare and poorly understood condition

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences