质子束照射配合抗血管内皮生长因子疗法治疗多形性脉络膜血管病:为期24个月的II期随机研究结果。

IF 2.4 3区 医学 Q2 OPHTHALMOLOGY
Wenyi Tang, Xianxin Qiu, Jingli Guo, Gezhi Xu, Lin Kong, Wei Liu
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引用次数: 0

摘要

目的:确定质子束照射(PBI)和抗血管内皮生长因子(anti-VEGF)疗法治疗多形性脉络膜血管病(PCV)/动脉瘤样1型黄斑新生血管(AT1)的有效性和安全性:这项随机临床试验由新确诊的PCV/AT1活动期患者组成,他们按1:1的比例随机接受最初每月三次的玻璃体内抗血管内皮生长因子药物(康柏西汀)注射治疗,同时接受或不接受单次14 GyE放射治疗。随后的抗血管内皮生长因子治疗按实际情况进行。主要结果指标包括抗血管内皮生长因子注射次数、最佳矫正视力(BCVA)和24个月时的视网膜中央厚度(CRT)。次要结局指标包括息肉病变消退率、息肉病变和分支血管网(BVN)面积的变化以及 24 个月时放疗相关不良事件:共有45只眼睛(86.5%)完成了24个月的随访。24个月时,联合疗法组比单一疗法组需要注射的抗血管内皮生长因子更少(5.9 ± 4.1 vs. 8.8 ± 5.3;P = 0.04)。两组的 BCVA 平均增益和 CRT 平均减幅无显著差异(分别为 P = 0.85 和 P = 0.17)。在息肉病变完全消退率(80.0% 对 48%,P = 0.03)和 BVN 面积变化率(- 1.03 ± 1.24 mm2 对 0.36 ± 0.77 mm2,P 结论:在息肉病变完全消退率(80.0% 对 48%,P = 0.03)和 BVN 面积变化率(- 1.03 ± 1.24 mm2 对 0.36 ± 0.77 mm2,P 结论:联合疗法优于单一疗法:PBI(14 GyE)联合抗血管内皮生长因子疗法可减少 PCV/AT1 对额外抗血管内皮生长因子注射的需求。需要进行更长时间的随访,以全面评估 PBI 的长期安全性:目前治疗 PCV/AT1 的主要方法包括抗血管内皮生长因子药物单药治疗或联合光动力疗法。然而,由于息肉消退率相对较低且复发率较高,一些病例需要多次重复注射,因此具有挑战性。新进展 质子射线照射治疗联合抗血管内皮生长因子药物可协同促进息肉消退和分支血管网收缩,减轻 PCV/AT1 患者的抗血管内皮生长因子治疗负担。放射性视网膜病变程度较轻,在24个月的随访中似乎没有明显的视觉效果。质子束照射是治疗PCV/AT1的一种新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proton beam irradiation with anti-VEGF therapy for polypoidal choroidal vasculopathy: results of a 24-month, phase II randomized study.

Purpose: To determine the efficacy and safety of proton beam irradiation (PBI) and anti-vascular endothelial growth factor (anti-VEGF) therapy for polypoidal choroidal vasculopathy (PCV)/ aneurysmal type 1 macular neovascularization (AT1).

Methods: The randomized clinical trial consisted of newly diagnosed active PCV/AT1 patients who were randomized 1:1 to treatment with three initial monthly intravitreal anti-VEGF agent (conbercept) injections with or without single 14 GyE radiation. Subsequent anti-VEGF therapy was given pro re nata. The primary outcome measures were number of anti-VEGF injections, best-corrected visual acuity (BCVA), and central retinal thickness (CRT) at 24 months. Secondary outcome measures included the polypoidal lesion regression rate, changes in the areas of polypoidal lesions and branching vascular network (BVN), and radiotherapy-related adverse events at 24 months.

Results: A total of 45 eyes (86.5%) completed the 24-month follow-up. At 24 months, the combination therapy group required fewer anti-VEGF injections compared with the monotherapy group (5.9 ± 4.1 vs. 8.8 ± 5.3; P = 0.04). The mean gains in BCVA and the mean decrease in CRT were not significantly different between the two groups (P = 0.85 and P = 0.17, respectively). Combination therapy was superior to monotherapy for complete polypoidal lesion regression (80.0% vs. 48%, P = 0.03) and change in BVN area (- 1.03 ± 1.24 mm2 vs. 0.36 ± 0.77 mm2, P < 0.01). The radiation-related microvascular abnormalities were observed in 55.0% of eyes following combination therapy at 15.7 ± 2.5 months.

Conclusion: PBI (14 GyE) combined with anti-VEGF therapy could decrease the need for additional anti-VEGF injections for PCV/AT1. Longer follow-up is needed to fully evaluate the long-term safety of PBI.

Key messages: What is known The current main methods for treating PCV/AT1 include anti-VEGF drugs as monotherapy or in combination with photodynamic therapy. However, some cases can be challenging with multiple repeated injections due to the relatively low regression rate of polyps and high recurrence rate. What is new Proton beam irradiation therapy with anti-VEGF drugs can synergistically promote the regression of polyps and the shrinkage of branching vascular network, and reduce the anti-VEGF treatment burden for patients with PCV/AT1. Radiation retinopathy was mild and did not appear to be visually significant at the 24-month follow-up. Proton beam irradiation can be a new strategy for the treatment of PCV/AT1.

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来源期刊
CiteScore
5.40
自引率
7.40%
发文量
398
审稿时长
3 months
期刊介绍: Graefe''s Archive for Clinical and Experimental Ophthalmology is a distinguished international journal that presents original clinical reports and clini-cally relevant experimental studies. Founded in 1854 by Albrecht von Graefe to serve as a source of useful clinical information and a stimulus for discussion, the journal has published articles by leading ophthalmologists and vision research scientists for more than a century. With peer review by an international Editorial Board and prompt English-language publication, Graefe''s Archive provides rapid dissemination of clinical and clinically related experimental information.
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