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Immune checkpoint inhibitor-related myositis and myocarditis in patients with cancer.
- Source :
-
Neurology [Neurology] 2018 Sep 04; Vol. 91 (10), pp. e985-e994. Date of Electronic Publication: 2018 Aug 08. - Publication Year :
- 2018
-
Abstract
- Objective: To report the clinicopathologic features and outcome of myositis in patients treated with immune checkpoint inhibitors (ICIs) (irMyositis).<br />Methods: We retrospectively analyzed patients diagnosed with irMyositis in tertiary centers in Paris, France, and Berlin, Germany, from January 2015 to July 2017. The main outcomes were clinical manifestations and muscle histology, which included major histocompatibility complex class I (MHC-I), C5b-9, CD3, CD4, CD8, CD20, CD68, programmed cell death protein 1 (PD-1), programmed cell death 1 ligand 1 (PD-L) 1, and programmed cell death 1 ligand 2 (PD-L2).<br />Results: Ten patients with metastatic cancer were included; median age was 73 (range 56-87) years. Median follow-up duration was 48 (range 16-88) weeks. Six patients developed myositis during nivolumab therapy, 1 patient during pembrolizumab, 1 patient during durvalumab, and 2 patients during combined nivolumab and ipilimumab. Median delay between ICI initiation and myositis onset was 25 (range 5-87) days. Clinical manifestations were dominated by acute or subacute myalgia (8 patients) and limb-girdle (7), axial (7), and oculomotor (7) weakness. Four patients had evidence of myocarditis. In all patients, creatine kinase levels were elevated (median 2,668, range 1,059-16,620 U/L), while anti-acetylcholine receptor and myositis-associated antibodies were negative. Electrodiagnostic studies showed myopathic process without decrement in all patients. Muscle biopsy constantly showed multifocal necrotic myofibers, sarcolemmal MHC-I, and endomysial inflammation, consisting mainly of CD68+ cells expressing PD-L1 and CD8+ cells expressing PD-1. ICI treatment was withdrawn in all patients; 9 patients received immunosuppressive therapy, which consistently led to marked clinical improvement.<br />Conclusions: irMyositis presents with remarkably homogeneous and unique clinicopathologic features, expanding the nosologic spectrum of inflammatory myopathies in patients with cancer. ICI withdrawal and treatment with corticosteroids improve outcome.<br /> (© 2018 American Academy of Neurology.)
- Subjects :
- Adolescent
Adult
Aged
Aged, 80 and over
Autoantibodies blood
Creatine Kinase metabolism
Electromyography
Europe
Female
Follow-Up Studies
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Muscle, Skeletal pathology
Myocardium pathology
Myositis diagnostic imaging
Receptor Protein-Tyrosine Kinases immunology
Receptors, Cholinergic immunology
Retrospective Studies
Young Adult
Apoptosis Regulatory Proteins metabolism
Cytokines metabolism
Myocarditis etiology
Myositis etiology
Neoplasms complications
Subjects
Details
- Language :
- English
- ISSN :
- 1526-632X
- Volume :
- 91
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 30089619
- Full Text :
- https://doi.org/10.1212/WNL.0000000000006124