新血管性年龄相关性黄斑变性改用法利昔单抗治疗后的实际治疗间隔和形态学结果。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Katrin Löw, Vasilena Sitnilska, Yuhe Tang, Jeany Q Lammert, Tim U Krohne, Lebriz Altay
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引用次数: 0

摘要

目的:评估法利昔单抗对其他VEGF抑制剂无效的新生血管性年龄相关性黄斑变性(nAMD)患者的疗效。方法:这项回顾性研究包括被诊断为nAMD的患者的眼睛,这些患者由于视网膜内液(IRF)和/或视网膜下液(SRF)的持续存在而切换到法利西单抗治疗,尽管使用治疗和延长方案每月使用阿非利塞普、贝伐单抗或雷尼单抗进行抗vegf治疗,并且在转换后接受了至少三次法利西单抗注射。每次就诊均进行最佳矫正视力(BCVA)测量和光学相干断层扫描(OCT)分析,OCT结果由两名独立阅读者评分。结果:纳入39例患者41眼(男21例,女18例),平均年龄80.5±8.1岁。在改用faricimab之前,抗vegf治疗的中位持续时间为5.0年,中位为53次注射。第一次给药后12只眼(29.3%)和第三次给药后15只眼(36.6%)的IRF和SRF完全消退。28只眼睛在至少12个月的转换后达到随访时间,中位数为10次法利西单抗注射。在这28只眼中,10只眼(35.7%)表现出完全的IRF/SRF分辨率;21只眼(80.7%)延长治疗间隔超过4周,8只眼(28.6%)在延长治疗间隔的情况下在第12个月出现完全的IRF/SRF消退。12个月后视网膜中央厚度中位数从368.0µm降至297.5µm (p < 0.001), BCVA保持稳定(p = 0.057)。在整个治疗期间没有不良事件的报告。结论:在抗vegf治疗反应较差的nAMD患者中,即使经过多年的治疗失败,改用faricimab也可以达到完全快速的液体溶解和延长治疗间隔。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-Life Treatment Intervals and Morphological Outcomes Following the Switch to Faricimab Therapy in Neovascular Age-Related Macular Degeneration.

Objectives: To evaluate the efficacy of faricimab in patients with neovascular age-related macular degeneration (nAMD) that did not respond to other VEGF inhibitors. Methods: This retrospective study included the eyes of patients diagnosed with nAMD who had been switched to faricimab treatment due to the persistence of intraretinal fluid (IRF) and/or subretinal fluid (SRF), despite monthly anti-VEGF treatment with aflibercept, bevacizumab, or ranibizumab using the treat and extend regimen, and who had received at least three faricimab injections following the switch. Best-corrected visual acuity (BCVA) measurement and optical coherence tomography (OCT) analysis were performed at each visit, and the OCT results were graded by two independent readers. Results: We included 41 eyes of 39 patients (21 male, 18 female) with a mean age of 80.5 ± 8.1 years. The median duration of anti-VEGF treatment prior to the switch to faricimab was 5.0 years, with a median of 53 injections. Complete resolution of IRF and SRF was observed after the first dose of faricimab in 12 eyes (29.3%) and after the third dose in 15 eyes (36.6%). Twenty-eight eyes reached a follow-up time after a switch of at least 12 months, with a median of 10 faricimab injections. Of these 28 eyes, 10 eyes (35.7%) exhibited complete IRF/SRF resolution; treatment intervals were extended beyond 4 weeks in 21 eyes (80.7%), and 8 eyes (28.6%) presented complete IRF/SRF resolution under extended treatment intervals at month 12. Central retinal thickness after 12 months was reduced from a median of 368.0 µm to 297.5 µm (p < 0.001), and the BCVA remained stable (p = 0.057). No adverse events were reported throughout the entire treatment period. Conclusions: In nAMD patients with poor anti-VEGF treatment response, complete and fast fluid resolution and the extension of treatment intervals can be reached by switching to faricimab, even after years of prior unsuccessful therapy.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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