Sato Shiori, Sakurada Yoichi, Fukuda Yoshiko, Kotoda Yumi, Kashiwagi Kenji
Department of Ophthalmology, University of Yamanashi, Chuo, JPN.
Cureus. 2025 Jun 16;17(6):e86113. doi: 10.7759/cureus.86113. eCollection 2025 Jun.
Vascular endothelial growth factor (VEGF) is critical in various retinal diseases. VEGF inhibitors are a standard treatment for neovascular age-related macular degeneration (AMD). However, intraocular inflammation (IOI) is a major complication after intravitreal administration of second-generation VEGF inhibitors. We report a case of IOI following treatment with aflibercept 8 mg in an eye with a history of IOI due to faricimab. An 83-year-old man was referred to our clinic and diagnosed with type 1 macular neovascularization (MNV), with a previous treatment history of four doses of ranibizumab, 14 doses of aflibercept (2 mg), and two doses of faricimab. The best-corrected visual acuity (BCVA) in the right eye was 0.3 in the decimal format. Treatment was initiated with an as-needed faricimab regimen after three consecutive monthly injections. Thirteen days after the ninth faricimab injection, the patient complained of blurred vision in the right eye. Mild inflammation, with small keratic precipitates (KPs), was observed in the anterior chamber. After topical dexamethasone administration (four times a day), the anterior chamber inflammation resolved one week after treatment. However, exudation recurred 13 weeks after the ninth faricimab administration; therefore, the intravitreal injection was switched to aflibercept 8 mg. Two days after switching to aflibercept 8 mg, the patient complained of pain and blurred vision in the right eye. As with the ninth faricimab injection, mild inflammation was observed in the anterior chamber of the right eye. One week after subtenon triamcinolone acetonide (STTA) and topical dexamethasone, inflammation disappeared in the anterior chamber. In eyes with a history of IOI, careful attention is needed when switching to aflibercept 8 mg from another second-generation VEGF inhibitor, including faricimab.
血管内皮生长因子(VEGF)在各种视网膜疾病中起着关键作用。VEGF抑制剂是治疗新生血管性年龄相关性黄斑变性(AMD)的标准疗法。然而,眼内炎症(IOI)是玻璃体内注射第二代VEGF抑制剂后的主要并发症。我们报告了1例在因法西单抗导致IOI病史的眼中使用8mg阿柏西普治疗后发生IOI的病例。一名83岁男性被转诊至我们的诊所,诊断为1型黄斑新生血管(MNV),既往有4剂雷珠单抗、14剂阿柏西普(2mg)和2剂法西单抗的治疗史。右眼的最佳矫正视力(BCVA)为小数格式的0.3。在连续每月注射3次后,开始按需使用法西单抗治疗方案。在第9次注射法西单抗13天后,患者抱怨右眼视力模糊。在前房中观察到轻度炎症,伴有少量角膜后沉着物(KP)。局部应用地塞米松(每日4次)后,治疗1周后前房炎症消退。然而,在第9次注射法西单抗13周后渗出复发;因此,玻璃体内注射改为8mg阿柏西普。改为8mg阿柏西普2天后,患者抱怨右眼疼痛和视力模糊。与第9次注射法西单抗时一样,右眼前房观察到轻度炎症。在球后注射曲安奈德(STTA)和局部应用地塞米松1周后,前房炎症消失。在有IOI病史的眼中,从另一种第二代VEGF抑制剂(包括法西单抗)转换为8mg阿柏西普时需要密切关注。