Tislelizumab-associated toxic epidermal necrolysis in an esophageal cancer patient: a case report.
증례보고
1/5 보강
[BACKGROUND] Tislelizumab, a humanized IgG4 anti-programmed cell death 1 (PD-1) monoclonal antibody approved in China in 2019 for advanced solid tumors such as esophageal cancer, functions by blocking
APA
Jin S, Liu Z, Zheng F (2025). Tislelizumab-associated toxic epidermal necrolysis in an esophageal cancer patient: a case report.. Frontiers in immunology, 16, 1707956. https://doi.org/10.3389/fimmu.2025.1707956
MLA
Jin S, et al.. "Tislelizumab-associated toxic epidermal necrolysis in an esophageal cancer patient: a case report.." Frontiers in immunology, vol. 16, 2025, pp. 1707956.
PMID
41268547 ↗
Abstract 한글 요약
[BACKGROUND] Tislelizumab, a humanized IgG4 anti-programmed cell death 1 (PD-1) monoclonal antibody approved in China in 2019 for advanced solid tumors such as esophageal cancer, functions by blocking the PD-1/PD-L1 pathway to reactivate anti-tumor immunity. Common adverse reactions include fever and rash; however, toxic epidermal necrolysis (TEN)-a rare, life-threatening drug hypersensitivity reaction-is reported in fewer than 0.1% of patients receiving PD-1 inhibitors, with limited real-world evidence specifically linking it to tislelizumab.
[CASE PRESENTATION] A 70-year-old male with esophageal squamous cell carcinoma received two cycles of neoadjuvant therapy (nab-paclitaxel, cisplatin, and tislelizumab 200 mg) followed by partial esophagectomy. On day 86 after the first tislelizumab infusion, he developed a diffuse rash progressing to skin exfoliation, vesiculation, and a positive Nikolsky sign, leading to a diagnosis of TEN. Upon admission, his SCORTEN was 3 (predicting 35% mortality) and ALDEN score was 5, indicating a probable association with tislelizumab. Management included intravenous methylprednisolone, immunoglobulin, topical treatments, and nutritional support. The patient achieved complete recovery two months after symptom onset.
[CONCLUSION] This case illustrates that tislelizumab can induce TEN after a prolonged incubation period (86 days in this instance). It underscores the importance of vigilant monitoring of skin and mucous membranes during treatment, early recognition and intervention, and adequate glucocorticoid dosing in managing this serious immune-related adverse event, offering valuable clinical insight for oncologists.
[CASE PRESENTATION] A 70-year-old male with esophageal squamous cell carcinoma received two cycles of neoadjuvant therapy (nab-paclitaxel, cisplatin, and tislelizumab 200 mg) followed by partial esophagectomy. On day 86 after the first tislelizumab infusion, he developed a diffuse rash progressing to skin exfoliation, vesiculation, and a positive Nikolsky sign, leading to a diagnosis of TEN. Upon admission, his SCORTEN was 3 (predicting 35% mortality) and ALDEN score was 5, indicating a probable association with tislelizumab. Management included intravenous methylprednisolone, immunoglobulin, topical treatments, and nutritional support. The patient achieved complete recovery two months after symptom onset.
[CONCLUSION] This case illustrates that tislelizumab can induce TEN after a prolonged incubation period (86 days in this instance). It underscores the importance of vigilant monitoring of skin and mucous membranes during treatment, early recognition and intervention, and adequate glucocorticoid dosing in managing this serious immune-related adverse event, offering valuable clinical insight for oncologists.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Stevens-Johnson Syndrome
- Aged
- Antibodies
- Monoclonal
- Humanized
- Esophageal Neoplasms
- Esophageal Squamous Cell Carcinoma
- Immune Checkpoint Inhibitors
- Antineoplastic Agents
- Immunological
- PD-1 inhibitor
- case report
- esophageal cancer
- immune-related adverse events
- tislelizumab
- toxic epidermal necrolysis
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