Li Angela S, Myers Justin, Stinnett Sandra S, Grewal Dilraj S, Jaffe Glenn J
Department of Ophthalmology, Duke University, Durham, North Carolina.
Ophthalmol Sci. 2023 Aug 13;4(2):100383. doi: 10.1016/j.xops.2023.100383. eCollection 2024 Mar-Apr.
To validate GATHER-1 inclusion criteria and the study's primary anatomic end point by assessing the reproducibility of geographic atrophy (GA) measurements and factors that affect reproducibility.
Post hoc analysis of phase II/III clinical trial.
All 286 participants included in the GATHER-1 study.
For each subject, blue-light fundus autofluorescence (FAF), color fundus photographs, fluorescein angiograms, and OCT scans were obtained on the study eye and fellow eye. Geographic atrophy area and other lesion characteristics were independently graded by 2 experienced primary readers. If the 2 readers differed on gradeability, GA area (> 10%) or other lesion characteristics, the image was graded by an arbitrator whose measurement or characterization was the final grade.
The main outcome measures were gradeability and reproducibility of FAF imaging data. Imaging data included lesion area, confluence of GA with peripapillary atrophy (PPA), whether GA involved the foveal centerpoint, and type of hyperautofluorescence pattern.
A total of 2004 images (1002 visits, 286 participants) were analyzed. Gradeability (90.5%) and interreader gradeability concordance (90.2%) were high across all visits. Study eye images were more gradable compared with fellow-eye images. A greater proportion of smaller lesions required arbitration, but interreader reproducibility was consistently high for all images. There was no difference in gradeability, gradeability concordance, or lesion-area concordance for images with PPA-confluent GA compared with those with nonconfluent PPA. Foveal centerpoint-involving lesions had lower gradeability and lesion-area concordance. Images with diffuse patterns of hyperautofluorescence had better gradeability and gradeability concordance than those with nondiffuse patterns but had no difference in lesion-area or lesion-area concordance.
There is high gradeability and excellent reproducibility measures across all images. These data support the validity of conclusions from GATHER-1 and the chosen inclusion criteria and end point.
Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
通过评估地图样萎缩(GA)测量的可重复性以及影响可重复性的因素,验证GATHER - 1纳入标准和该研究的主要解剖学终点。
II/III期临床试验的事后分析。
GATHER - 1研究纳入的所有286名参与者。
为每位受试者的研究眼和对侧眼获取蓝光眼底自发荧光(FAF)、彩色眼底照片、荧光素血管造影和光学相干断层扫描(OCT)图像。地图样萎缩面积和其他病变特征由2名经验丰富的主要阅片者独立分级。如果2名阅片者在分级能力、GA面积(>10%)或其他病变特征上存在差异,则由一名仲裁者对图像进行分级,其测量或特征描述即为最终分级。
主要观察指标为FAF成像数据的分级能力和可重复性。成像数据包括病变面积、GA与视乳头周围萎缩(PPA)的融合情况、GA是否累及黄斑中心点以及高自发荧光模式的类型。
共分析了2004张图像(1002次就诊,286名参与者)。在所有就诊中,分级能力(90.5%)和阅片者间分级能力一致性(90.2%)都很高。与对侧眼图像相比,研究眼图像更易于分级。较小病变需要仲裁的比例更高,但所有图像的阅片者间可重复性始终很高。与PPA不融合的GA图像相比,PPA融合的GA图像在分级能力、分级能力一致性或病变面积一致性方面没有差异。累及黄斑中心点的病变分级能力和病变面积一致性较低。具有弥漫性高自发荧光模式的图像比非弥漫性模式的图像具有更好的分级能力和分级能力一致性,但在病变面积或病变面积一致性方面没有差异。
所有图像均具有较高的分级能力和出色的可重复性指标。这些数据支持GATHER - 1研究结论以及所选纳入标准和终点的有效性。
本文末尾的脚注和披露中可能会找到专有或商业披露信息。