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Malignancy Risk and Predictors in Dermatomyositis and Polymyositis: A Large Population-Based Study
Yonatan Shneor Patt1,2, Niv Ben-Shabat1,3, Paula David1,2,4
1Department of Internal Medicine B & Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel-Hashomer, Ramat Gan 5262100, Israel.
Idiopathic inflammatory myopathies (IIMs) increase cancer risk, particularly dermatomyositis (DM) which is linked to solid and blood cancers. Specific autoantibodies and older age at diagnosis predict higher malignancy risk in DM and polymyositis (PM).
Area of Science:
- Rheumatology and Oncology
- Autoimmune Diseases and Cancer Epidemiology
Background:
- Idiopathic inflammatory myopathies (IIMs) are rare autoimmune disorders with known associations with malignancy, especially in dermatomyositis (DM).
- Previous studies on malignancy predictors in IIMs are limited by small sample sizes and lack of population-based data.
- Understanding site-specific cancer patterns and risk factors in large, diverse IIM cohorts is crucial.
Purpose of the Study:
- To evaluate malignancy patterns and identify predictors in a large, diverse cohort of patients with DM and polymyositis (PM).
- To assess the association between IIM subtypes and the risk of both solid and hematologic malignancies.
- To determine specific autoantibodies and clinical factors associated with increased cancer risk in IIM patients.
Main Methods:
- Retrospective cohort study utilizing the Clalit Health Services electronic database (2002-2018).
- Inclusion of 1557 DM patients and 528 PM patients, matched with controls at a 1:5 ratio.
- Analysis of malignancy incidence and risk using Cox proportional hazards models and logistic regression for predictors.
Main Results:
- DM showed a significantly increased risk for both solid and hematologic malignancies (HR 1.89), while PM had a less pronounced association limited to solid cancers (HR 1.50).
- In DM, elevated risks were observed for breast cancer (HR 1.86) and chronic leukemia (HR 5.02).
- Older age at diagnosis and specific autoantibodies (antiphospholipid, lupus anticoagulant, anti-Mi2, various antinuclear antibodies) were associated with increased malignancy risk across both subtypes.
Conclusions:
- Both DM and PM are associated with an increased risk of malignancy, with DM exhibiting a broader association including hematologic cancers.
- Older age and a distinct serological profile, particularly antiphospholipid and antinuclear antibodies, are key predictors of heightened malignancy risk.
- Heightened clinical vigilance is warranted for IIM patients with these risk factors to facilitate early cancer detection.
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