Bressler Neil, Haskova Zdenka, Kapre Audrey, Gentile Brittany
Wilmer Eye Institute, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Genentech, Inc., South San Francisco, CA, USA.
Transl Vis Sci Technol. 2024 Dec 2;13(12):27. doi: 10.1167/tvst.13.12.27.
To derive estimates of clinically meaningful change (improvement) on the 25-item National Eye Institute Visual Function Questionnaire (NEI VFQ-25) in patients with diabetic macular edema (DME) using anchor- and distribution-based methods.
In this exploratory post hoc analysis of data from the RIDE/RISE (NCT00473382/NCT00473330) clinical trials of ranibizumab for DME, the NEI VFQ-25 was completed at baseline and six, 12, 18, and 24 months. Anchor-based (≥5-, ≥10-, and ≥15-letter gain in best-corrected visual acuity [BCVA]) and distribution-based estimates were calculated. Subgroup analyses included outcomes when the study eye was the better- or worse-seeing eye.
Baseline characteristics were balanced between the trials (RIDE, N = 382; RISE, N = 377). Anchor-based estimates of clinically meaningful improvement in composite scores (for ≥15-letter gain in BCVA) were 3.78 and 2.23 for RIDE and RISE, respectively. Estimates appeared similar for most subscales: near activities (4.11 and 3.31), distance activities (3.53 and 3.74), driving difficulties (5.15 and 3.15), and vision-specific dependency (4.70 and 1.83). Supportive distribution-based meaningful change composite score estimates also were similar between RIDE and RISE for values based on 0.5 standard deviation (9.85 and 9.70, respectively) or standard error of the mean (5.10 and 4.82, respectively).
These analyses suggest improvement of three to five points on the NEI VFQ-25 composite score and four individual subscales as clinically meaningful in patients with DME.
This analysis supports considering these thresholds when assessing the clinical risk-benefit of DME treatment from the patient perspective using the NEI VFQ-25.
采用基于锚定和分布的方法,得出糖尿病性黄斑水肿(DME)患者在25项美国国立眼科研究所视觉功能问卷(NEI VFQ - 25)上具有临床意义的变化(改善)估计值。
在这项对雷珠单抗治疗DME的RIDE/RISE(NCT00473382/NCT00473330)临床试验数据的探索性事后分析中,在基线以及6、12、18和24个月时完成NEI VFQ - 25评估。计算基于锚定的(最佳矫正视力[BCVA]提高≥5、≥10和≥15字母)和基于分布的估计值。亚组分析包括研究眼为视力较好或较差眼时的结果。
两项试验(RIDE,N = 382;RISE,N = 377)的基线特征均衡。基于锚定的复合评分临床意义改善估计值(BCVA提高≥15字母),RIDE为3.78,RISE为2.23。大多数子量表的估计值相似:近视力活动(4.11和3.31)、远视力活动(3.五3和3.74)、驾驶困难(5.15和3.15)以及视力相关依赖(4.70和1.83)。基于分布的支持性有意义变化复合评分估计值在RIDE和RISE之间也相似,基于0.5标准差的值分别为9.85和9.70,基于均值标准误的值分别为5.10和4.82。
这些分析表明,DME患者在NEI VFQ - 25复合评分上提高三到五分以及四个单独子量表上的变化具有临床意义。
该分析支持在从患者角度使用NEI VFQ - 25评估DME治疗的临床风险效益时考虑这些阈值。