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替雷利珠单抗致晚期食管鳞状细胞癌患者双器官功能障碍:一例报告

Tislelizumab induced dual organs dysfunction in a patient with advanced esophageal squamous cell carcinoma: a case report.

作者信息

Yang Bo, Gou Wei, Lan Naiying, Shao Qing, Hu Weifeng, Xue Cheng, Liu Nanmei

机构信息

Internal Medicine III (Nephrology), Naval Medical Center of PLA, Naval Medical University, Shanghai, China.

Department of Nephrology and Endocrinology, Shanghai 411 Hospital, Shanghai University, Shanghai, China.

出版信息

Front Oncol. 2024 Mar 14;14:1347896. doi: 10.3389/fonc.2024.1347896. eCollection 2024.


DOI:10.3389/fonc.2024.1347896
PMID:38549923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10972938/
Abstract

BACKGROUND: Tislelizumab, a humanized IgG4 anti-PD-1 monoclonal antibody has been approved in China and Europe. According to the published clinical research, tislelizumab shows satisfactory safety profile. No severe hepatotoxicity or acute kidney injury were reported. CASE PRESENTATION: We presented a case study of a 74-year-old man who developed acute kidney injury (grade 3) and acute liver injury (grade 4) after being administered tislelizumab for the treatment of esophageal squamous cell carcinoma. We reviewed the patient's history, physical examination, and laboratory findings and provided comprehensive differentials of the possible causes of the toxicities. Immune Checkpoint Inhibitors (ICI) hepatotoxicity and nephrotoxicity were confirmed clinically. We also discussed the management of toxicities associated with ICIs and the need for a multidisciplinary approach to care. CONCLUSIONS: The case highlights the importance of close monitoring and prompt management of toxicities associated with ICIs and the need for further research to better understand the risk factors for these toxicities and to identify effective treatments for them.

摘要

背景:替雷利珠单抗是一种人源化IgG4抗程序性死亡蛋白1(PD-1)单克隆抗体,已在中国和欧洲获批。根据已发表的临床研究,替雷利珠单抗显示出令人满意的安全性。未报告严重肝毒性或急性肾损伤。 病例介绍:我们报告了一例74岁男性患者的病例研究,该患者在接受替雷利珠单抗治疗食管鳞状细胞癌后发生急性肾损伤(3级)和急性肝损伤(4级)。我们回顾了患者的病史、体格检查和实验室检查结果,并对毒性反应的可能原因提供了全面的鉴别诊断。临床确诊为免疫检查点抑制剂(ICI)肝毒性和肾毒性。我们还讨论了与ICI相关毒性的管理以及多学科护理方法的必要性。 结论:该病例强调了密切监测和及时处理与ICI相关毒性的重要性,以及进一步研究以更好地了解这些毒性的危险因素并确定有效治疗方法的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2026/10972938/db9c7c4384b9/fonc-14-1347896-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2026/10972938/db9c7c4384b9/fonc-14-1347896-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2026/10972938/db9c7c4384b9/fonc-14-1347896-g001.jpg

相似文献

[1]
Tislelizumab induced dual organs dysfunction in a patient with advanced esophageal squamous cell carcinoma: a case report.

Front Oncol. 2024-3-14

[2]
RATIONALE 311: tislelizumab plus concurrent chemoradiotherapy for localized esophageal squamous cell carcinoma.

Future Oncol. 2021-11

[3]
Tislelizumab plus chemotherapy versus placebo plus chemotherapy as first-line treatment for advanced or metastatic oesophageal squamous cell carcinoma (RATIONALE-306): a global, randomised, placebo-controlled, phase 3 study.

Lancet Oncol. 2023-5

[4]
Tislelizumab versus chemotherapy as second-line treatment for European and North American patients with advanced or metastatic esophageal squamous cell carcinoma: a subgroup analysis of the randomized phase III RATIONALE-302 study.

ESMO Open. 2024-1

[5]
Immune checkpoint inhibitors chemotherapy as second-line therapy for advanced oesophageal squamous cell carcinoma: a systematic review and economic evaluation.

Therap Adv Gastroenterol. 2024-2-28

[6]
Tislelizumab: A Modified Anti-tumor Programmed Death Receptor 1 Antibody.

Cancer Control. 2022

[7]
Tislelizumab versus chemotherapy as second-line treatment of advanced or metastatic esophageal squamous cell carcinoma (RATIONALE 302): impact on health-related quality of life.

ESMO Open. 2022-8

[8]
Adrenal crisis mainly manifested as recurrent syncope secondary to tislelizumab: a case report and literature review.

Front Immunol. 2023

[9]
Tislelizumab: an investigational anti-PD-1 antibody for the treatment of advanced non-small cell lung cancer (NSCLC).

Expert Opin Investig Drugs. 2020-12

[10]
Pamiparib in combination with tislelizumab in patients with advanced solid tumours: results from the dose-escalation stage of a multicentre, open-label, phase 1a/b trial.

Lancet Oncol. 2019-8-1

引用本文的文献

[1]
Tislelizumab-induced anaphylactic shock: a case report.

Discov Oncol. 2025-7-10

[2]
The differentiation and intervention strategies for acute kidney injury after or induced by immune checkpoint inhibitors.

Am J Cancer Res. 2025-4-15

本文引用的文献

[1]
Perioperative immunotherapy for esophageal squamous cell carcinoma: Now and future.

World J Gastroenterol. 2023-9-14

[2]
Tislelizumab plus chemotherapy versus placebo plus chemotherapy as first-line treatment for advanced or metastatic oesophageal squamous cell carcinoma (RATIONALE-306): a global, randomised, placebo-controlled, phase 3 study.

Lancet Oncol. 2023-5

[3]
Esophageal and Esophagogastric Junction Cancers, Version 2.2023, NCCN Clinical Practice Guidelines in Oncology.

J Natl Compr Canc Netw. 2023-4

[4]
Risk factors associated with immune checkpoint inhibitor-induced acute kidney injury compared with other immune-related adverse events: a case-control study.

Clin Kidney J. 2022-4-28

[5]
Acute Kidney Injury Induced by Immune Checkpoint Inhibitors.

Kidney Dis (Basel). 2022-4-4

[6]
Immune Checkpoint Inhibitors in Cancer Therapy.

Curr Oncol. 2022-4-24

[7]
Tislelizumab Versus Chemotherapy as Second-Line Treatment for Advanced or Metastatic Esophageal Squamous Cell Carcinoma (RATIONALE-302): A Randomized Phase III Study.

J Clin Oncol. 2022-9-10

[8]
Abnormal liver enzymes: A review for clinicians.

World J Hepatol. 2021-11-27

[9]
Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: ASCO Guideline Update.

J Clin Oncol. 2021-12-20

[10]
Immune checkpoint inhibitor-related hepatotoxicity: A review.

World J Gastroenterol. 2021-8-28

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