Neuromuscular adverse events associated with anti-PD-1 monoclonal antibodies: Systematic review.
Adrenal Cortex Hormones
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ adverse effects
Antineoplastic Agents, Immunological
/ adverse effects
Humans
Immunoglobulins, Intravenous
/ therapeutic use
Immunologic Factors
/ therapeutic use
Muscular Diseases
/ chemically induced
Myasthenia Gravis
/ chemically induced
Myositis
/ chemically induced
Neuromuscular Diseases
/ chemically induced
Nivolumab
/ adverse effects
Peripheral Nervous System Diseases
/ chemically induced
Plasma Exchange
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
02 04 2019
02 04 2019
Historique:
received:
30
09
2018
accepted:
10
01
2019
pubmed:
10
3
2019
medline:
18
12
2019
entrez:
10
3
2019
Statut:
ppublish
Résumé
Neuromuscular adverse events following cancer treatment with anti-programmed cell death protein 1 (PD-1) monoclonal antibodies are relatively rare, yet potentially fatal. We performed a systematic review to characterize the clinical presentation, diagnostic workup, and management of neuromuscular disorders (NMDs) in patients treated with nivolumab or pembrolizumab monotherapy or concurrent with other immunologic agents, such as ipilimumab. Sixty-one publications on 85 patients (mean age 66.9 years [range 34-86]; male/female 2.6:1; 59% metastatic melanoma) were identified from selected indexing databases until June 2018. Forty-eight patients had received nivolumab and 39 pembrolizumab. The mean number of PD-1 inhibitor treatment cycles prior to onset of symptoms was 3.6 (range 1-28). Symptoms included oculomotor (47%), respiratory (43%), bulbar (35%), and proximal weakness (35%), as well as muscle pain (28%). Diagnoses were categorized as myasthenia gravis (27%), neuropathy (23%), myopathy (34%), or a combination of these (16%). After a critical review of the data, however, evidence did not support the stated NMD diagnosis in 13% of cases, while up to 25% of patients had signs of additional NMDs. Cardiac complications occurred in more than 30% of patients diagnosed with myasthenia gravis or myositis. Mortality was high in these patients, despite adequate treatment strategies including corticosteroid, IV immunoglobulins, and plasma exchange. The clinical presentation of NMDs associated with PD-1 inhibitors is often atypical, with considerable overlap between myasthenia gravis and myopathy, and cardiac/respiratory complications are common.
Identifiants
pubmed: 30850443
pii: WNL.0000000000007235
doi: 10.1212/WNL.0000000000007235
doi:
Substances chimiques
Adrenal Cortex Hormones
0
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents, Immunological
0
Immunoglobulins, Intravenous
0
Immunologic Factors
0
Programmed Cell Death 1 Receptor
0
Nivolumab
31YO63LBSN
pembrolizumab
DPT0O3T46P
Types de publication
Journal Article
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
663-674Informations de copyright
© 2019 American Academy of Neurology.