Retinal Toxicity after Initial Administration of Nivolumab and Ipilimumab

IF 0.7 Q4 OPHTHALMOLOGY
A. Kilani, Efstathios Vounotrypidis, Susanna F. König, Armin Wolf
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Abstract

Background. To present a rare case of a bilateral immune checkpoint inhibitor- (ICI-) induced photoreceptor injury with a bacillary layer detachment (BALAD) and a dissection of the photoreceptor inner and outer segment, accompanied by ICI-induced Vogt-Koyanagi-Harada- (VKH-) like uveitis after initial administration of nivolumab and ipilimumab. Case Presentation. A 52-year-old female with metastatic malignant cutaneous melanoma experiencing bilateral progressive visual acuity reduction, after treatment initiation with 1 mg/kg nivolumab and 3 mg/kg ipilimumab two weeks prior symptom onset. An extensive laboratory workup, including uveitis workup, onconeuronal and retinal antibodies, ruled out a paraneoplastic autoimmune disorder and a granulomatous disease. Furthermore, a B-scan was performed to exclude a posterior scleritis. Ensuing temporary treatment discontinuation of nivolumab and complete discontinuation of ipilimumab, treatment with high-dose systemic steroids was initiated, which resulted in alleviation of her symptoms and stability of ocular findings. Conclusions. ICIs can induce significant ocular side effects. As ocular inflammation can be well controlled using systemic steroids, treatment with ICIs can be continued whenever possible, in particular, if there is a good treatment response of the systemic malignancy.
首次使用 Nivolumab 和 Ipilimumab 后的视网膜毒性
背景。介绍一例罕见的双侧免疫检查点抑制剂(ICI)诱导的光感受器损伤病例,该病例在首次使用 nivolumab 和 ipilimumab 后,光感受器内节和外节发生了包膜层脱落(BALAD)和剥离,并伴有 ICI 诱导的类似 Vogt-Koyanagi-Harada- (VKH-) 的葡萄膜炎。病例介绍。一名 52 岁女性,患有转移性恶性皮肤黑色素瘤,在症状出现前两周开始接受 1 毫克/千克 nivolumab 和 3 毫克/千克 ipilimumab 治疗后,双侧视力逐渐下降。广泛的实验室检查(包括葡萄膜炎检查、肿瘤细胞抗体和视网膜抗体)排除了副肿瘤性自身免疫性疾病和肉芽肿性疾病的可能性。此外,还进行了 B 型扫描,以排除后巩膜炎。在暂时停用 nivolumab 和完全停用 ipilimumab 后,她开始接受大剂量全身类固醇治疗,结果症状得到缓解,眼部检查结果也趋于稳定。结论ICIs 可引起明显的眼部副作用。由于使用全身性类固醇可以很好地控制眼部炎症,因此可以尽可能继续使用 ICIs 治疗,尤其是在全身性恶性肿瘤治疗反应良好的情况下。
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14 weeks
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