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深度学习辅助分析治疗抵抗性新生血管性年龄相关性黄斑变性患者从阿柏西普2毫克剂量增加至8毫克后生物标志物的变化

Deep learning-assisted analysis of biomarker changes after increase of dosing from aflibercept 2 mg to 8 mg in therapy-resistant neovascular age-related macular degeneration.

作者信息

Hafner Michael, Asani Ben, Eckardt Franziska, Liesenhoff Caspar, Kufner Alexander, Siedlecki Jakob, Schworm Benedikt, Priglinger Siegfried, Schiefelbein Johannes Benedikt

机构信息

Department of Ophthalmology, LMU University Hospital, LMU Munich, Munich, BY, Germany.

Department of Ophthalmology, LMU University Hospital, LMU Munich, Munich, BY, Germany

出版信息

BMJ Open Ophthalmol. 2025 Jun 1;10(1):e002176. doi: 10.1136/bmjophth-2025-002176.

Abstract

PURPOSE

Age-related macular degeneration (AMD) remains the leading cause of blindness in developed countries. There are many different intravitreal anti-vascular endothelial growth factor (VEGF) drugs available for the treatment of neovascular AMD (nAMD). Unfortunately, not all patients respond equally well to the drugs, and some show recurrences during treatment. Since 01/2024, aflibercept 8 mg represents an additional treatment option and contains a four times higher dosage than the already known aflibercept 2 mg.

METHODS

To evaluate the real-world efficacy of aflibercept 8 mg in refractory nAMD patients, focusing on changes in key optical coherence tomography biomarkers over a follow-up period of the first four aflibercept 8 mg injections using a deep learning-based semantic segmentation algorithm. Inclusion criteria were: switch to aflibercept 8 mg after insufficient response to aflibercept 2 mg, marked by persistent retinal fluid or inability to extend treatment beyond 6 weeks; completion of at least 3 months (90 days) follow-up under treat-and-extend treatment regime; and no confounding conditions like intraocular infection, uveitis or other retinal diseases.

RESULTS

23 eyes of 21 patients with therapy-resistant nAMD were switched to aflibercept 8 mg. All patients had previously received aflibercept 2 mg, with an average of 30.7 previous anti-VEGF injections. Significant reductions in intraretinal fluid and fibrovascular pigment epithelial detachment at timepoint V3 were observed. The decrease in subretinal fluid and central retinal thickness at V3 was not significant. Treatment intervals extended significantly by 24%, from a baseline average of 34 days to 42 days. Best-corrected visual acuity remained stable throughout the study period.

CONCLUSIONS

Aflibercept 8 mg demonstrated significant efficacy and durability in reducing nAMD biomarkers and extending intervals in a real-world setting. The use of deep learning for biomarker quantification highlighted its potential for enhancing treatment monitoring and decision-making. Future studies with a larger patient cohort and prospective study setting should explore long-term outcomes and integration of artificial intelligence-driven analysis.

摘要

目的

年龄相关性黄斑变性(AMD)仍是发达国家失明的主要原因。有许多不同的玻璃体内抗血管内皮生长因子(VEGF)药物可用于治疗新生血管性AMD(nAMD)。不幸的是,并非所有患者对这些药物的反应都同样良好,有些患者在治疗期间会复发。自2024年1月起,8毫克阿柏西普成为一种额外的治疗选择,其剂量是已知的2毫克阿柏西普的四倍。

方法

为了评估8毫克阿柏西普在难治性nAMD患者中的实际疗效,重点关注使用基于深度学习的语义分割算法在首次注射8毫克阿柏西普后的四个注射周期的随访期间关键光学相干断层扫描生物标志物的变化。纳入标准为:在对2毫克阿柏西普反应不足后改用8毫克阿柏西普,表现为持续性视网膜积液或无法将治疗延长超过6周;在治疗并延长治疗方案下完成至少3个月(90天)的随访;且无眼内感染、葡萄膜炎或其他视网膜疾病等混杂情况。

结果

21例治疗抵抗性nAMD患者的23只眼改用8毫克阿柏西普。所有患者此前均接受过2毫克阿柏西普治疗,平均先前接受过30.7次抗VEGF注射。在V3时间点观察到视网膜内积液和纤维血管色素上皮脱离显著减少。V3时视网膜下积液和中心视网膜厚度的减少不显著。治疗间隔显著延长了24%,从基线平均34天延长至42天。在整个研究期间,最佳矫正视力保持稳定。

结论

在实际应用中,8毫克阿柏西普在减少nAMD生物标志物和延长治疗间隔方面显示出显著的疗效和持久性。使用深度学习进行生物标志物定量突出了其在加强治疗监测和决策方面的潜力。未来更大患者队列和前瞻性研究设置的研究应探索长期结果以及人工智能驱动分析的整合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d5/12142079/5f9f09a201f7/bmjophth-10-1-g001.jpg

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