中国药物警戒 ›› 2025, Vol. 22 ›› Issue (10): 1165-1167.
DOI: 10.19803/j.1672-8629.20241005

• 安全与合理用药 • 上一篇    下一篇

斯鲁利单抗致老年结肠肿瘤患者多器官免疫性损伤1例分析

李小梅, 王洪贵*, 孙嘉婧   

  1. 四川省成都市都江堰市人民医院,四川 成都 611830
  • 收稿日期:2024-12-20 出版日期:2025-10-15 发布日期:2025-10-20
  • 通讯作者: *王洪贵,男,硕士,主任药师,医院药学。E-mail: 71700330@qq.com
  • 作者简介:李小梅,女,硕士,副主任药师,临床药学。

One Case of Multi-Organ Immune Injury Caused by Serplulimab in an Elderly Patient with Colon Tumor

LI Xiaomei, WANG Honggui*, SUN Jiajing   

  1. Dujiangyan People's Hospital, Chengdu Sichuan 611830, China
  • Received:2024-12-20 Online:2025-10-15 Published:2025-10-20

摘要: 目的 探讨斯鲁利单抗致多器官免疫性损伤的不良反应,为临床安全用药提供参考。方法 对1例斯鲁利单抗致老年结肠肿瘤患者多器官免疫性损伤的病例进行分析,并结合相关文献进行归纳和总结。结果 根据患者的临床表现、实验室检查及用药时间关联性,斯鲁利单抗致多器官免疫性损伤为很可能,经停用斯鲁利单抗,给予糖皮质激素治疗后患者好转出院,但因患者院外未遵医嘱用药及未监测不良反应等最终导致不良反应进展。结论 免疫检查点抑制剂致多器官免疫性损伤发生率较低,但致死率较高。临床在应用斯鲁利单抗治疗前加强风险评估,用药期间严密监测,注意斯鲁利单抗致多器官免疫性损伤的风险。

关键词: 斯鲁利单抗, 心肌炎, 重症肌无力, 肌炎, 程序性死亡受体1, 免疫检查点抑制剂

Abstract: Objective To investigate such adverse reactions as multi-organ immune injury induced by serplulimab, and to provide a reference for safe clinical practice. Methods One case of multi-organ immune injury induced by serplulimab in an elderly patient with colon tumors was analyzed, and a summary was made after literature review. Results Based on the patient's clinical manifestations, results of laboratory tests, and the temporal association with drug administration,the patient's multi-organ immune injury was considered to have been caused by serplulimab. The patient improved and was discharged after glucocorticoid therapy. However, the adverse reactions progressed because the patient failed to take the prescribed drugs or monitor for adverse reactions after discharge. Conclusion The incidence of ICIs-associated multi-organ immune injury is relatively low, but the fatality is exceedingly high. Clinicians should assess the risk before administering serplulimab, closely monitor patients during treatment, and remain alert to the risk of serplulimab-induced multi-organ immune injury.

Key words: Serplulimab, Myocarditis, Myasthenia gravis, Myositis, PD-1, ICIs

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