Abstract

Immune checkpoint inhibitors (ICI) and their associated immune related cutaneous adverse events (irCAEs) are continuing to become a mainstay of cancer treatment regimens. While most rashes are mild and easily manageable, severe or persistent rashes like lichenoid dermatoses can significantly impact quality of life and may require ICI cessation. Lichenoid dermatoses currently have no management guidelines beyond the use of topical or oral steroids. Our study is the first large-scale retrospective chart review to characterize ICI-induced lichenoid eruptions, their treatments, and associated tumor response. We used natural language processing and our institutional medical record to identify 119 patients with lichenoid eruptions on ICI therapy. Of those, 108 rashes were characterized as lichenoid dermatitis and fifteen as lichenoid mucositis. Most patients presented with a diffuse distribution (86%, 101/117), with pruritus in lichenoid dermatoses (82%, 89/108) and pain in lichenoid mucositis (80%, 12/15). Successful treatments for lichenoid dermatitis included topical steroids (81%, 88/108), oral antihistamines (21%, 23/108), and oral steroids (15%, 16/108). Of lichenoid dermatitis patients, 21% (23/108) either did not respond to treatment (7) or required oral steroids (16). Approximately 28% of patients who had lichenoid dermatitis had a dose impact on their ICI because of the irCAE,which is significantly greater than the average 5-10% dose impact of most irCAEs. This descriptive study highlights the importance of lichenoid dermatitis and the need for more effective nonsteroidal management strategies.

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