Fatal immune-related hepatitis with intrahepatic cholestasis and pneumonia associated with camrelizumab: A case report and literature review

被引:13
作者
Tan, Youwen [1 ]
Ye, Yun [1 ]
Chen, Li [1 ]
机构
[1] Jiangsu Univ, Hosp Zhenjiang Affiliated 3, Dept Hepatol, 300 Daijiamen, Zhenjiang 212003, Jiangsu, Peoples R China
来源
OPEN MEDICINE | 2021年 / 16卷 / 01期
关键词
camrelizumab; immune-related hepatitis; intrahepatic cholestasis; immune-related pneumonia;
D O I
10.1515/med-2021-0267
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Camrelizumab (SHR-1210), a humanmonoclonal antibody against programmed death receptor 1 (PD-1), blocks the binding of PD-1 to PD-L1, consequently inhibiting immune system evasion by tumor cells. A 65-year-old man underwent radical esophagectomy 5 months ago following the diagnosis of esophageal cancer by gastroscopy. Approximately 40 days later, capecitabine was administered at a dosage of 1.5 g Po bid for 14 days, and anti-PD-1 (camrelizumab 200 mg) was administered twice. Around 20 days later, abnormal liver function was detected. He received a diagnosis of drug-induced liver injury. Chest computed tomography scanning revealed interstitial inflammatory lesions in both lower lungs. Liver biopsy revealed immune injury with ductopenia. Therefore, the diagnosis was revised as immune-related pneumonia and hepatitis associated with camrelizumab. The treatment regimen of methylprednisolone was adjusted to 40 mg/day and gradually increased to 80 mg/day. Mycophenolate mofetil was administered at a dose of 2 g/day. Consequently, chest tightness and shortness of breath resolved, and pulmonary inflammation improved. However, jaundice did not improve and continued to exacerbate. The last measured prothrombin time was 41 s, prothrombin activity was 19%, and the international normalized ratio was 4.03. The cause of death was diagnosed as liver failure, cardiopulmonary failure, and septic shock.
引用
收藏
页码:553 / 557
页数:5
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