Journal Article10.1097/rhu.0000000000001874
Immune Checkpoint Inhibitor–Associated Myositis
Didem Saygin,Pauline Doucet +1 more
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TL;DR: In this paper , an expertise-based classification criterion was proposed to provide a standardized definition of ICI myositis and allow comparability between studies, which is a critical need for prospective translational and clinical studies that elucidate the pathophysiology of these patients in order to improve evaluation and management of those patients.
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Abstract: Research on the relationship between inflammatory myopathy and malignancy has grown considerably within the last century. Now, the burgeoning field of inflammatory myopathy has yet another player in the mix: immune checkpoint inhibitor-associated myositis (ICI myositis). Immune checkpoint inhibitor-associated myositis is indicated by clinical diagnosis of inflammatory myopathy after initiation of immune checkpoint inhibitor for cancer management. Current literature reflects low prevalence but high mortality associated with ICI myositis, especially when involving myasthenia gravis and myocarditis. Immune checkpoint inhibitor-associated myositis tends to have muscle pain along with weakness, infrequent presentation with dermatitis, or interstitial lung disease and is typically seronegative with scattered, endomysial inflammatory infiltrates on biopsy. The differential diagnosis of ICI myositis includes myasthenia gravis and other neurological immune-related adverse events. Therapeutic approach involves high doses of corticosteroids with a choice of steroid-sparing immunomodulating agent(s) that is primarily driven by expert opinion due to lack of robust research to support one agent over another. There is wide variation in the inclusion criteria for ICI myositis used in previous studies. We review previously used inclusion criteria and suggest an expertise-based classification criterion to provide a standardized definition and allow comparability between studies. There is a critical need for prospective translational and clinical studies that elucidate the pathophysiology of ICI myositis in order to improve evaluation and management of these patients.
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The Need for Classification Criteria of Immune Checkpoint Inhibitor-Induced Inflammatory Arthritis
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1
References
A case report of immune checkpoint inhibitor-related steroid-refractory myocarditis and myasthenia gravis-like myositis treated with abatacept and mycophenolate mofetil
TL;DR: A case of steroid-refractory ICI-related myocarditis and myositis treated with abatacept and mycophenolate mofetil and gradual subjective improvement and termination of arrhythmia led to discharge of the patient from the hospital 6 weeks after the introduction of ICI.
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Neurological disorders associated with immune checkpoint inhibitors: an association with autoantibodies.
TL;DR: Among diverse neurological immune-related adverse events (irAEs), autoimmune encephalitis, aseptic meningitis, Guillain-Barre syndrome (GBS), myasthenia gravis (MG), and myositis are particularly important as mentioned in this paper.
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Bilateral Facial Palsy following Ipilimumab Infusion for Melanoma.
TL;DR: A patient who developed new-onset bilateral facial palsy following infusion of ipilimumab is reported, which is believed to be the first reported case of its kind in the United States.
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Immune checkpoint inhibitors (ICIs)-related ocular myositis.
Matteo Garibaldi,Fabio Calabrò,Gioia Merlonghi,Silvia Pugliese,Marco Ceccanti,Lara Cristiano,Tommaso Tartaglione,Antonio Petrucci +7 more
TL;DR: The findings support this clinical entity, suggesting that isolated ocular myositis represents a subgroup of generalised Myositis with predominant ocular symptoms.
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Cardiac Troponin I and T in Checkpoint Inhibitor-associated Myositis and Myocarditis.
TL;DR: In this paper, the authors reported a case of a patient with severe ir-myositis while on adjuvant programmed cell death protein 1 inhibitor immunotherapy for stage III melanoma, with accompanying elevation in troponin I (cTnI) without apparent clinical evidence of myocardial injury.
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