Myositis as a neuromuscular complication of immune checkpoint inhibitors.


Journal

Acta neurologica Belgica
ISSN: 2240-2993
Titre abrégé: Acta Neurol Belg
Pays: Italy
ID NLM: 0247035

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 04 09 2019
accepted: 15 01 2020
pubmed: 30 1 2020
medline: 24 11 2020
entrez: 30 1 2020
Statut: ppublish

Résumé

Immune checkpoint inhibitors (ICI) induce improved clinical outcomes associated with numerous cancers, but immune-related adverse events can occur, including neuromuscular complications. We searched for all muscle biopsies from the patient data system of University Hospitals Leuven (UZ Leuven) from January 2014 to July 2018 (n = 686) and collected clinical data of patients with a biopsy-proven ICI-related myositis and expanded the pathological examinations. We identified three cases of ICI-related myositis in patients with malignant melanoma. The clinical phenotype ranged from mild to life threatening. Two patients had a myositis-myasthenia gravis overlap syndrome and one had a co-occurring myocarditis. Pathological examination showed a necrotizing and/or inflammatory myopathy with CD4 + and CD8 + T cells and CD68 + macrophages. IgG staining was positive in all cases. PD-1 and PD-L1 reactions were negative for inhibitors of the PD-1/PD-L1 pathway (nivolumab, atezolizumab) and positive for CTLA-4 inhibitors (ipilimumab). With increasing usage of ICI, clinicians must be aware of rare but potentially serious adverse events such as myositis. Early detection by inquiring about complaints and clinical signs of weakness and monitoring the creatine phosphokinase level in serum are recommended. Our histological findings are in line with other reports. The IgG positivity suggests a local role of the ICI in the pathophysiology of the myositis. Further research must be performed to identify patients at risk and to optimize treatment of the complications.

Identifiants

pubmed: 31993961
doi: 10.1007/s13760-020-01282-w
pii: 10.1007/s13760-020-01282-w
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Ipilimumab 0
Nivolumab 31YO63LBSN
atezolizumab 52CMI0WC3Y

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

355-364

Subventions

Organisme : Fonds Wetenschappelijk Onderzoek
ID : G0F8516N
Organisme : Universitaire Ziekenhuizen Leuven, KU Leuven
ID : C14-17-107
Organisme : CSL Behring
ID : Emil von Behring Chair for Neuromuscular and Neurodegenerative Disorders

Auteurs

Lynn Vermeulen (L)

Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. vermeulen_lynn@hotmail.com.

Christophe E Depuydt (CE)

Laboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, KU Leuven, Leuven, Belgium.

Petra Weckx (P)

Department of Pathology, University Hospitals Leuven, Leuven, Belgium.

Oliver Bechter (O)

Department of Oncology, University Hospitals Leuven, Leuven, Belgium.

Philip Van Damme (P)

Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
Center for Brain and Disease Research, VIB, KU Leuven, Leuven, Belgium.

Dietmar R Thal (DR)

Department of Pathology, University Hospitals Leuven, Leuven, Belgium.
Laboratory for Neuropathology, Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.

Kristl G Claeys (KG)

Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
Laboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, KU Leuven, Leuven, Belgium.

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Classifications MeSH