Vogt-Koyanagi-Harada disease during chemoimmunotherapy for non-small cell lung cancer.
Yuri KuronoTakayuki TakedaYusuke KunimatsuNozomi TaniIzumi HashimotoKazuki HirosePublished in: Respirology case reports (2020)
Vogt-Koyanagi-Harada disease (VKHD) is a rare systemic granulomatous autoimmune disease that affects melanocyte-rich organs such as eye, inner ear, meninges, skin, and hair. VKHD leads to chronic uveal inflammation accompanied by a decline in visual acuity in some patients when appropriate corticosteroid treatment was not initiated in an early phase. Immune checkpoint inhibitors (ICIs) are widely used in the treatment of several kinds of cancers and chemoimmunotherapy has become the standard of care in the first-line treatment of non-small cell lung cancer (NSCLC). While ICIs induce immune-related adverse events, drug-induced VKHD is quite rare with only four reports in the ICI monotherapy; three patients with melanoma and one patient with NSCLC. We describe the first case of VKHD during chemoimmunotherapy including pembrolizumab in a patient with NSCLC, which was successfully treated with corticosteroid without any sequela.
Keyphrases
- drug induced
- liver injury
- small cell lung cancer
- advanced non small cell lung cancer
- case report
- healthcare
- combination therapy
- end stage renal disease
- multiple sclerosis
- ejection fraction
- newly diagnosed
- oxidative stress
- clinical trial
- palliative care
- quality improvement
- young adults
- epidermal growth factor receptor
- replacement therapy
- pain management
- open label
- chronic pain
- patient reported
- wound healing
- electronic health record
- smoking cessation
- idiopathic pulmonary fibrosis