Pembrolizumab-Induced Ocular Myasthenic Crisis.

anti-pd-1 diplopia immune checkpoint inhibitor keytruda myasthenia gravis myasthenic crisis ocular pembrolizumab ptosis

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
14 Jul 2020
Historique:
entrez: 21 7 2020
pubmed: 21 7 2020
medline: 21 7 2020
Statut: epublish

Résumé

Pembrolizumab, one of many novel immune checkpoint inhibitors (ICPi), is a monoclonal antibody that enhances immunity against cancer cells. Extensive escalation in immune activity predisposes to unsought immune-related adverse events. Due to progressive mesothelioma, a 67-year-old man was referred to the research unit and enrolled in a clinical trial with a cluster of differentiation (CD) 27 chemotherapeutic agent. He began crossover treatment and received just two doses of pembrolizumab, 33 and 16 days prior to admission. He subsequently presented to the emergency department with three days of acute onset severe diplopia and a drooping left eye. Acetylcholine receptor (AChR) antibodies returned positive at 13.9 nmol/L, and a diagnosis of ocular myasthenia gravis (OMG) was made. During his hospitalization, the patient was managed with methylprednisolone 80 mg intravenously daily, with conversion to prednisone 60 mg by mouth daily at time of discharge. Neuro-ophthalmology consultation was sought in the outpatient setting, and the patient was started on pyridostigmine. He was readmitted two weeks later with symptoms of progressive diffuse weakness, unsteady gait, and dysphagia, all in the setting of persistent diplopia. Intravenous immunoglobulin (IVIG) was promptly initiated, in addition to the pyridostigmine previously initiated in the outpatient setting. Unfortunately, after three IVIG treatments, the patient had experienced little improvement in his symptoms, and therefore elected hospice care. Although ICPis have revolutionized the management of a multitude of malignancies, recognition of immune-related adverse events is of critical importance.

Identifiants

pubmed: 32685327
doi: 10.7759/cureus.9192
pmc: PMC7366038
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e9192

Informations de copyright

Copyright © 2020, Lorenzo et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

J Oncol Pract. 2018 Apr;14(4):247-249
pubmed: 29517954
Indian J Ophthalmol. 2014 Oct;62(10):985-91
pubmed: 25449931
Muscle Nerve. 2016 Sep;54(3):507
pubmed: 27121245
Eur J Cancer. 2017 Sep;82:128-136
pubmed: 28666240
J Neurooncol. 2018 May;137(3):601-609
pubmed: 29332184
Melanoma Res. 2017 Apr;27(2):152-154
pubmed: 27776019
Intern Med. 2019 Jun 1;58(11):1635-1638
pubmed: 30713313
Clin Exp Ophthalmol. 2019 Aug;47(6):796-798
pubmed: 30859689
Neurology. 2017 Sep 12;89(11):1127-1134
pubmed: 28821685

Auteurs

Christian J Lorenzo (CJ)

Internal Medicine, Sarasota Memorial Hospital, Florida State University College of Medicine, Sarasota, USA.

Haley Fitzpatrick (H)

Pharmacy, Sarasota Memorial Hospital, Sarasota, USA.

Victoria Campdesuner (V)

Internal Medicine, Sarasota Memorial Hospital, Florida State University College of Medicine, Sarasota, USA.

Justin George (J)

Internal Medicine, Sarasota Memorial Hospital, Florida State University College of Medicine, Sarasota, USA.

Natalia Lattanzio (N)

Internal Medicine, Sarasota Memorial Hospital, Florida State University College of Medicine, Sarasota, USA.

Classifications MeSH