A Case of Delayed Immune Checkpoint Inhibitor Hepatitis in a Patient with Malignant Melanoma

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Dayna Telken, Nael Haddad, Victor Arce Gutierrez, Donald Tschirhart, Yasmin Alishahi
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Abstract

Immune checkpoint inhibitors are an increasingly utilized class of medications in oncology. Significant adverse effects have been reported, including hepatitis which mostly occurs early after initiating treatment. We present a case of a 78-year-old male with past medical history of recurrent sinusoidal mucosal malignant melanoma on pembrolizumab for three years that presented with painless jaundice of 72-hour duration. Laboratory evaluation demonstrated alkaline phosphatase at 1780 IU/L, aspartate aminotransferase at 2290 IU/L, alanine aminotransferase at 1224 IU/L, and bilirubin of 10.0 mg/dL with direct bilirubin of 7.4 mg/dL. The patient underwent interventional radiology transjugular liver biopsy demonstrating features of drug-induced liver injury secondary to pembrolizumab therapy. He was started on steroid therapy and completed six-week course with resolution in liver enzymes. This is a unique case in which pembrolizumab-induced hepatitis occurred three years after initiation of treatment. Due to the increased use of immune checkpoint inhibitors for oncologic treatment, it is important for clinicians to recognize their immune-related adverse effects and varying timing in which these toxicities may occur.
恶性黑色素瘤患者迟发性免疫检查点抑制剂肝炎1例
免疫检查点抑制剂是肿瘤学中越来越多使用的一类药物。据报道,严重的不良反应,包括肝炎,主要发生在开始治疗后的早期。我们提出一个病例78岁的男性既往病史复发的窦粘膜恶性黑色素瘤的派姆单抗三年,表现为无痛黄疸72小时的持续时间。实验室评估显示碱性磷酸酶为1780 IU/L,天冬氨酸转氨酶为2290 IU/L,丙氨酸转氨酶为1224 IU/L,胆红素为10.0 mg/dL,直接胆红素为7.4 mg/dL。患者接受介入放射经颈静脉肝活检,显示派姆单抗治疗继发的药物性肝损伤特征。他开始接受类固醇治疗,并完成了为期六周的疗程,肝酶水平有所改善。这是一个独特的病例,其中派姆单抗诱导肝炎发生在开始治疗三年后。由于免疫检查点抑制剂在肿瘤治疗中的使用越来越多,临床医生认识到它们与免疫相关的不良反应和这些毒性可能发生的不同时间是很重要的。
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