Immune checkpoint inhibitor-related myositis and myocarditis in patients with cancer

医学 肌炎 免疫系统 内科学 心肌炎 免疫检查点 癌症 免疫学 免疫疗法
作者
Mehdi Touat,Thierry Maisonobe,Samuel Knauß,Omar Ben Hadj Salem,B. Hervier,Karine Auré,Tali‐Anne Szwebel,N. Kramkimel,Claire Lethrosne,Jean-Frédéric Bruch,Pauline Laly,Jacques Cadranel,Nicolas Weiss,Anthony Béhin,Yves Allenbach,Olivier Benveniste,Timothée Lenglet,Dimitri Psimaras,Werner Stenzel,Sarah Léonard-Louis
出处
期刊:Neurology [Ovid Technologies (Wolters Kluwer)]
卷期号:91 (10) 被引量:294
标识
DOI:10.1212/wnl.0000000000006124
摘要

To report the clinicopathologic features and outcome of myositis in patients treated with immune checkpoint inhibitors (ICIs) (irMyositis).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).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 ICI treatment was withdrawn in all patients; 9 patients received immunosuppressive therapy, which consistently led to marked clinical improvement.irMyositis presents with remarkably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.
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