To explore the clinical characteristics of sintilimab-induced Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and provide references for prevention, diagnosis, and treatment. Clinical reports of sintilimab-induced SJS/TEN published before March 31st, 2026 were collected by searching the database, and clinical data were extracted for retrospective analysis. Twenty-three men (69.7%) and ten women (30.3%) were included, with a median age of 66 years (range: 27, 82). The median time for the appearance of SJS/TEN was 20 days (range: 2, 240), and the median cycle was 1 cycle (range: 1, 17). Among these 33 patients, 72.7% were diagnosed with TEN, 15.2% with SJS, and 12.1% with SJS/TEN overlap. The main clinical symptoms were rash (75.0%), erosion (82.1%), bullae/blisters (78.6%), erythema (67.9%), epidermal detachment (57.1%), and pruritus (50.0%), high fever (46.4%), and ocular symptoms (35.7%). Furthermore, 57.6% of the patients experienced mucosal lesions, mainly affecting the mouth (89.5%), genitalia (57.9%), and conjunctiva (52.6%). Skin biopsy showed poptotic keratinocytes (83.3%), subepidermal blisters (50.0%), and inflammatory cell infiltration (100%). After discontinuing sintilimab and receiving systemic steroids and intravenous immunoglobulins (IVIG) treatment, 87.9% of the patients experienced improvement in skin symptoms, while 12.1% of the patients died from TEN. SJS/TEN is a rare and life-threatening cutaneous adverse reaction of sintilimab. During the use of sintilimab, clinicians should be aware of the possibility of SJS/TEN, especially within the first month. For patients diagnosed with SJS/TEN, sintilimab should be discontinued, and they should receive systemic steroids and IVIG treatment.
No takes yet. Share an insight, caveat, or question.
Wu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: