Chronic and Severe Non-Lichenoid Oral Ulcers Induced by Nivolumab - Diagnostic and Therapeutic Challenge: A Case Report

被引:7
作者
Cardona, Andres F. [1 ,2 ,3 ]
Ruiz-Patino, Alejandro [2 ,3 ]
Ricaurte, Luisa [2 ,3 ]
Lucia Zatarain-Barron, Zyanya [4 ]
Barron, Feliciano [4 ]
Arrieta, Oscar [4 ]
机构
[1] Clin Country, Clin & Translat Oncol Grp, Bogota, Colombia
[2] Fdn Clin & Appl Canc Res FICMAC, Bogota, Colombia
[3] Univ El Bosque, Mol Oncol & Biol Syst Res Grp Fox G, Calle 116 9-72,C 318, Bogota 110111, Colombia
[4] Natl Canc Inst INCan, Thorac Oncol Unit, Mexico City, DF, Mexico
关键词
Head and neck cancer; Oral ulcer; Immunotherapy; Toxicity; Microbiome analysis; PEMBROLIZUMAB; HEAD;
D O I
10.1159/000505968
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Due to the widespread use of immune checkpoint inhibitors and the growing research efforts in this area, immune-mediated toxicity is well recognized. Nonetheless, few severe cases of oral or upper gastrointestinal tract mucosal involvement have been documented. Early recognition and prompt treatment are key to the adequate management of these patients. We present a male 93-year-old patient with an advanced head and neck tumor treated with nivolumab who developed severe oral ulcers. After discontinuation of nivolumab, he received initial steroid treatment without any significant improvement. Histopathologic analysis of the lesions revealed a pattern similar to graft versus host disease. Extrapolating the results of colchicine mouth washing in patients with active oral ulcers and Behcet's disease, this strategy was implemented with concomitant metronomic cyclophosphamide, achieving complete ulcer resolution. Metagenomic oral bacterial sequencing during instauration of the lesions and highest extension revealed a significant decrease in microbiomic diversity and expansion of Haemophilus parainfluenzae similar to patients with active Behcet's disease. In conclusion, oral ulcers associated with immune checkpoint inhibitors correspond to a difficult-to-treat entity that could physiopathologically be related to both graft versus host disease and Behcet's disease.
引用
收藏
页码:314 / 320
页数:7
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