Six-year findings of polypoidal choroidal vasculopathy in the EVEREST II study: Japanese subgroup analysis.

IF 2.1 3区 医学 Q2 OPHTHALMOLOGY
Yasuo Yanagi, Ryusaburo Mori, Kelvin Yi Chong Teo, Kyu-Hyung Park, Nor Fariza Ngah, Shih-Jen Chen, Paisan Ruamviboonsuk, Nagako Kondo, Won Ki Lee, Rajesh Rajagopalan, Ryo Obata, Ian Y H Wong, Caroline Chee, Hiroko Terasaki, Tetsuju Sekiryu, Shih-Chou Chen, Timothy Y Y Lai, Gemmy Cheung, Shigeru Honda
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引用次数: 0

Abstract

Purpose: To evaluate long-term outcomes for polypoidal choroidal vasculopathy (PCV) in Japanese patients in the EVEREST II study.

Study design: A multicenter, cross-sectional study of the long-term outcomes of a cohort of patients originally treated with ranibizumab alone (monotherapy group) or in combination with photodynamic therapy PDT (combination group) in the EVEREST II study (ClinicalTrials.gov identifier, NCT01846273).

Methods: Ninety participants from the six-year EVEREST II follow-up: 20 Japanese and 70 non-Japanese were included. Long-term changes in best-corrected visual acuity (BCVA) and central subfield thickness (CST) were reported in the Japanese compared to non-Japanese participants. Number of injections, types of anti-vascular endothelial growth factor (VEGF) agents used, and cases with equal visits and injections, indicating fixed dosing or treat-and-extend (TAE) administration were investigated. Outcomes were also compared between those who had verteporfin PDT during the six-year period (n=14) and those who did not (n=6).

Results: The Japanese and non-Japanese participants had similar baseline characteristics. The mean age for Japanese participants was 76±4.47 years, with 25% being women. BCVA improved from baseline to year 2 in both groups (P < 0.05). At six years, BCVA was maintained in the Japanese (67.2 ETDRS letters) but decreased in the non-Japanese participants (from 68.8 to 53.5 letters). The Japanese participants received more injections than the non-Japanese (12.5 vs. 7.57, P=0.017). Aflibercept was the most frequently used anti-VEGF agent, and the number of fixed dosing or TAE administration was higher in the Japanese participants. No significant differences were found in functional and anatomical outcomes between those who received PDT and those who did not (all P > 0.05). However, non-PDT participants had numerically worse BCVA at the final visit.

Conclusions: This study highlights positive long-term outcomes for Japanese PCV patients and underscores the need for further research to validate these findings in broader patient populations.

EVEREST II研究中6年发现的息肉样脉络膜血管病变:日本亚组分析。
目的:在EVEREST II研究中评估日本患者的息肉样脉络膜血管病变(PCV)的长期预后。研究设计:在EVEREST II研究(ClinicalTrials.gov identifier, NCT01846273)中,对最初接受雷尼单抗(单药治疗组)或联合光动力疗法PDT(联合组)治疗的患者进行多中心、横断面研究。方法:90名参与者来自6年EVEREST II随访:20名日本人和70名非日本人。与非日本参与者相比,日本参与者报告了最佳矫正视力(BCVA)和中央子视野厚度(CST)的长期变化。研究调查了注射次数、使用的抗血管内皮生长因子(VEGF)药物类型,以及就诊和注射次数相等的病例,表明固定剂量或治疗延长(TAE)给药。结果还比较了在6年期间接受维替泊芬PDT治疗的患者(n=14)和没有接受维替泊芬PDT治疗的患者(n=6)。结果:日本和非日本参与者具有相似的基线特征。日本参与者的平均年龄为76±4.47岁,其中25%为女性。从基线到第2年,两组的BCVA均有所改善(P < 0.05)。6年时,日本受试者的BCVA维持在67.2个ETDRS字母,而非日本受试者的BCVA下降(从68.8个字母降至53.5个字母)。日本参与者比非日本参与者接受更多的注射(12.5比7.57,P=0.017)。Aflibercept是最常用的抗vegf药物,并且固定剂量或TAE给药的次数在日本参与者中较高。在功能和解剖结果方面,接受PDT治疗的患者与未接受PDT治疗的患者无显著差异(均P < 0.05)。然而,非pdt参与者在最后一次就诊时的BCVA数值更差。结论:本研究强调了日本PCV患者的积极长期结果,并强调需要进一步研究以在更广泛的患者人群中验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
65
审稿时长
6-12 weeks
期刊介绍: The Japanese Journal of Ophthalmology (JJO) was inaugurated in 1957 as a quarterly journal published in English by the Ophthalmology Department of the University of Tokyo, with the aim of disseminating the achievements of Japanese ophthalmologists worldwide. JJO remains the only Japanese ophthalmology journal published in English. In 1997, the Japanese Ophthalmological Society assumed the responsibility for publishing the Japanese Journal of Ophthalmology as its official English-language publication. Currently the journal is published bimonthly and accepts papers from authors worldwide. JJO has become an international interdisciplinary forum for the publication of basic science and clinical research papers.
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