眼科 ›› 2026, Vol. 35 ›› Issue (4): 259-263.doi: 10.13281/i.cnki.issn.1004-4469.2026.04.002

• 论著 • 上一篇    下一篇

抗体药物偶联物相关眼部不良反应的特征分析

高斐   吴宇涵   姜洋   李莹   陈迪   赵潺   

  1. 中国医学科学院北京协和医学院,北京协和医院眼科; 眼底病智能诊断及药械研发与转化北京市重点实验室; 中国医学科学院眼底病重点实验室,北京 100730
  • 收稿日期:2026-05-03 出版日期:2026-07-25 发布日期:2026-07-25
  • 通讯作者: 赵潺,Email:zhaochan@pumch.cn

Analysis of the characteristics of drug-related ocular adverse reactions in antibody-drug conjugate cancer therapy

Gao Fei, Wu Yuhan, Jiang Yang, Li Ying, Chen Di, Zhao Chan   

  1. Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College; Beijing Key Laboratory of Fundus Diseases Intelligent Diagnosis & Drug/Device Development and Translation; Key Laboratory of Ocular Fundus Diseases, Chinese Academy of Medical Sciences, Beijing 100730, China
  • Received:2026-05-03 Online:2026-07-25 Published:2026-07-25
  • Contact: Zhao Chan, Email: zhaochan@pumch.cn

摘要: 目的  探讨抗体药物偶联物(antibody-drug conjugate, ADC)在肿瘤治疗中产生的药物相关眼部不良反应的临床特征。设计 回顾性病例系列研究。研究对象  2024年3月至2024年12月在中国医学科学院北京协和医院治疗的ADC药物眼部不良反应的患者7例(14眼)。方法  纳入接受ADC治疗肿瘤并发眼部不良反应的患者,进行眼科检查,记录并分析其发生药物相关眼部不良反应的类型、级别。主要指标  症状发生率、体征发生率、视力下降发生率、不同级别的不良反应发生率。结果  患者男性6例,女性1例,平均年龄(55.6±3.2)岁。所有患者均双眼受累,不良反应的症状包括:眼红(85.8%)、异物感(57.1%)、视物模糊(57.1%)、流泪(42.9%)及眼痒(14.3%);不良反应的体征包括:眼部充血(85.8%)、结膜水肿(71.4%)、分泌物增多(57.1%)、睑球粘连(42.9%)、假膜(42.9%)、滤泡增生(42.9%)、角膜上皮粗糙(42.9%)、角膜上皮缺损(28.6%)、角膜混浊(14.3%)、角膜新生血管(14.3%);不良反应累及视力下降程度:视力下降1行(42.9%)、视力下降2行(21.4%)、视力下降3行(14.3%)、视力下降5行及以上(21.4%);药物相关眼部不良反应导致的二级病变占比42.9%、三级病变占比28.6%、四级病变占比28.6%。所有患者经抗炎、对症治疗后,眼部病变最终均得到了稳定地控制。结论  应用ADC药物治疗肿瘤有发生眼部不良反应的潜在风险,需给予重视、进行密切随访及积极治疗。

关键词: 抗体药物偶联物, 药物不良反应, 眼毒性, 结膜炎, 角膜炎

Abstract: Objective To explore the clinical characteristics of drug-related ocular adverse reactions caused by antibody-drug conjugates (ADC) in tumor treatment. Design Retrospective case series. Participants  7 patients (14 eyes) with ocular adverse reactions to ADC who were treated at the Chinese Academy of Medical Sciences Peking Union Medical College Hospital from March 2024 to December 2024. Methods Clinical patients who received ADC-based tumor treatment and had ocular adverse reactions were included. Comprehensive ophthalmic examinations were conducted, and the types and grades of drug-related ocular adverse reactions were recorded and analyzed. Main Outcome Measures Incidence of symptoms, incidence of signs, incidence of visual acuity decline, and incidence of different lesion grades. Results There were 6 male patients and 1 female patient, with an average age of 55.6±3.2 years. All patients had bilateral involvement. The related adverse reaction symptoms included: eye redness (85.8%), foreign body sensation (57.1%), blurred vision (57.1%), tearing (42.9%), and eye itching (14.3%); The related adverse reaction signs included: ocular congestion (85.8%), conjunctival edema (71.4%), increased secretions (57.1%), eyelid-scleral adhesion (42.9%), pseudomembrane (42.9%), follicular hyperplasia (42.9%), rough corneal epithelium (42.9%), corneal epithelial defect (28.6%), corneal opacity (14.3%), and corneal neovascularization (14.3%); During the lesion process, the most severe situation of visual acuity decline was: visual acuity decline of 1 line (42.9%), visual acuity decline of 2 lines (21.4%), visual acuity decline of 3 lines (14.3%), and visual acuity decline of 5 lines or more (21.4%); The proportion of grade 2, grade 3, and grade 4 drug-related ocular adverse reactions was 42.9%, 28.6%, and 28.6%, respectively. After anti-inflammatory and symptomatic treatment, the ocular lesion conditions of all patients were ultimately stabilized. Conclusions The use of ADC for tumor treatment has the potential risk of causing severe ocular adverse reactions. It is necessary to pay sufficient attention, conduct close follow-up, and actively treat.


Key words: Antibody-drug conjugate, Adverse drug reaction, Ocular toxicity, Conjunctivitis, Keratitis