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2
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3
CHECKPOINT INHIBITOR IMMUNE THERAPY: Systemic Indications and Ophthalmic Side Effects.检查点抑制剂免疫治疗:全身适应证和眼部不良反应。
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Eye (Lond). 2018 Feb;32(2):287-301. doi: 10.1038/eye.2017.222. Epub 2017 Oct 20.
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Safety of checkpoint inhibitors for cancer treatment: strategies for patient monitoring and management of immune-mediated adverse events.癌症治疗中检查点抑制剂的安全性:患者监测及免疫介导不良事件管理策略
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Cancer Treat Rev. 2017 May;56:1-7. doi: 10.1016/j.ctrv.2017.03.011. Epub 2017 Apr 9.
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新型抗肿瘤生物治疗的眼部副作用。

Ocular side effects of novel anti-cancer biological therapies.

机构信息

The Ocular Oncology Service, The Goldschleger Eye Institute, Sheba Medical Center, Tel Hashomer, Israel.

Institute of Oncology, Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Sci Rep. 2021 Jan 12;11(1):787. doi: 10.1038/s41598-020-80898-7.

DOI:10.1038/s41598-020-80898-7
PMID:33436995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7803740/
Abstract

To examine the ocular side effects of selected biological anti-cancer therapies and the ocular and systemic prognosis of patients receiving them. We retrospectively reviewed all medical records of patients who received biological anti-cancer treatment from 1/2012 to 12/2017 and who were treated at our ocular oncology service. The following data was retrieved: primary malignancy, metastasis, type of biological therapy, ocular side effects, ophthalmic treatment, non-ocular side effects, and ocular and systemic disease prognoses. Twenty-two patients received biological therapies and reported ocular side effects. Eighteen patients (81.8%) had bilateral ocular side effects, including uveitis (40.9%), dry eye (22.7%), and central serous retinopathy (22.7%). One patient (4.5%) had central retinal artery occlusion (CRAO), and one patient (4.5%) had branch retinal vein occlusion (BRVO). At the end of follow-up, 6 patients (27.27%) had resolution of the ocular disease, 13 patients (59.09%) had stable ocular disease, and 3 patients (13.64%) had progression of the ocular disease. Visual acuity improved significantly at the end of follow-up compared to initial values. Eighteen patients (81.8%) were alive at study closure. Biological therapies can cause a wide range of ocular side effects ranging from dry eye symptoms to severe pathologies that may cause ocular morbidity and vision loss, such as uveitis, CRAO and BRVO. All patients receiving biological treatments should be screened by ophthalmologists before treatment, re-screened every 4-6 months during treatment, and again at the end of treatment. Patients on biological treatment who have ocular complaints should be urgently referred to ocular consultation for early identification and early intervention.

摘要

检查选定的生物抗癌疗法的眼部副作用以及接受这些疗法的患者的眼部和全身预后。我们回顾性分析了 2012 年 1 月至 2017 年 12 月期间在我们眼部肿瘤科接受生物抗癌治疗的所有患者的病历。检索了以下数据:原发恶性肿瘤、转移、生物治疗类型、眼部副作用、眼部治疗、非眼部副作用以及眼部和全身疾病预后。22 名患者接受了生物治疗并报告了眼部副作用。18 名患者(81.8%)出现双侧眼部副作用,包括葡萄膜炎(40.9%)、干眼症(22.7%)和中心性浆液性视网膜病变(22.7%)。1 名患者(4.5%)发生视网膜中央动脉阻塞(CRAO),1 名患者(4.5%)发生视网膜分支静脉阻塞(BRVO)。随访结束时,6 名患者(27.27%)眼部疾病缓解,13 名患者(59.09%)眼部疾病稳定,3 名患者(13.64%)眼部疾病进展。与初始值相比,随访结束时视力明显提高。18 名患者(81.8%)在研究结束时存活。生物疗法可引起多种眼部副作用,从干眼症症状到可能导致眼部发病率和视力丧失的严重疾病,如葡萄膜炎、CRAO 和 BRVO。所有接受生物治疗的患者在治疗前均应由眼科医生进行筛查,在治疗期间每 4-6 个月复查一次,并在治疗结束时再次复查。接受生物治疗且有眼部不适的患者应紧急转至眼科会诊,以便及早发现和干预。