Vogt-Koyanagi-Harada disease-like uveitis after drug therapy including BRAF/MEK inhibitors in melanoma patients with HLA-DRB1*04.
Ryo AmagaiTaku FujimuraEmi YamazakiManami TakahashiErika TamabuchiYumi KambayashiAkira HashimotoKazuki HashimotoYoshihide AsanoPublished in: The Journal of dermatology (2023)
The combination of BRAF kinase inhibitors (BRAFis) and MEK kinase inhibitors (MEKis) is one of the most promising chemotherapy regimens in the treatment of BRAF-mutant melanoma. Although BRAFi plus MEKi combined therapy is widely used for the treatment of BRAF V600 -mutated melanoma, the incidence of uveitis caused by BRAFi plus MEKi is limited. In this report, we described five cases (two men and three women) of Vogt-Koyanagi-Harada (VKH) disease-like uveitis in melanoma patients who received BRAFi plus MEKi combined therapy. Of note, all the patients had the HLA-DRB1*04 haplotype, which is frequently detected in VKH-like non-infectious uveitis. On the other hand, among BRAFi plus MEKi-treated patients who did not develop VKH disease-like uveitis, only one of five (20%) patients had the HLA-DRB1*04 haplotype. Collectively, BRAFi/MEKi might induce severe VKH disease-like uveitis in melanoma patients with the HLA-DRB1*04 haplotype.
Keyphrases
- juvenile idiopathic arthritis
- ankylosing spondylitis
- ejection fraction
- end stage renal disease
- newly diagnosed
- wild type
- stem cells
- rheumatoid arthritis
- metastatic colorectal cancer
- type diabetes
- pregnant women
- risk factors
- patient reported outcomes
- squamous cell carcinoma
- metabolic syndrome
- polycystic ovary syndrome
- cell therapy
- bone marrow
- insulin resistance
- early onset
- pi k akt
- skeletal muscle
- patient reported
- combination therapy
- locally advanced
- adverse drug
- rectal cancer