| Literature DB >> 27086869 |
Yves Allenbach1, Jeremy Keraen2, Anne-Marie Bouvier3, Valérie Jooste3, Nicolas Champtiaux2, Baptiste Hervier2, Yoland Schoindre2, Aude Rigolet2, Laurent Gilardin2, Lucile Musset4, Jean-Luc Charuel4, Olivier Boyer5, Fabienne Jouen5, Laurent Drouot5, Jeremie Martinet5, Tanya Stojkovic6, Bruno Eymard6, Pascal Laforêt6, Antony Behin6, Emmanuelle Salort-Campana7, Olivier Fain8, Alain Meyer9, Nicolas Schleinitz10, Kuberaka Mariampillai11, Aurelie Grados2, Olivier Benveniste11.
Abstract
Cancer can occur in patients with inflammatory myopathies. This association is mainly observed in dermatomyositis, and myositis-specific antibodies have allowed us to delineate patients at an increased risk. Malignancy is also reported in patients with necrotizing autoimmune myopathies, but the risk remains elusive. Anti-signal recognition particle or anti-HMGCR antibodies have been specifically associated with necrotizing autoimmune myopathies. We aimed at screening the incidence of cancer in necrotizing autoimmune myopathies. A group of patients (n = 115) with necrotizing autoimmune myopathies with or without myositis-specific antibodies was analysed. Malignancy occurred more frequently in seronegative necrotizing autoimmune myopathies patients and in HMGCR-positive patients compared to anti-signal recognition particle positive patients. Synchronous malignancy was diagnosed in 21.4% and 11.5% of cases, respectively, and incidence of cancer was higher compared to the general population in both groups. No specific type of cancer was predominant. Patients suffering from a synchronous cancer had a decreased median survival time. Cancer screening is necessary in seronegative necrotizing autoimmune myopathies and in HMGCR-positive patients but not in anti-signal recognition particle-positive patients.Entities:
Keywords: auto-antibodies; cancer; necrotizing autoimmune myopathies; polymyositis
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Year: 2016 PMID: 27086869 DOI: 10.1093/brain/aww054
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501