Retina Specialists of Beverly Hills, Beverly Hills, California.
Genentech Inc, South San Francisco, California.
JAMA Ophthalmol. 2021 Feb 1;139(2):219-223. doi: 10.1001/jamaophthalmol.2020.5130.
Pigment epithelial detachment (PED) is a feature commonly associated with neovascular age-related macular degeneration (nAMD) and may be perceived as being difficult to treat. Therefore, this investigation explored changes in PEDs and visual acuity outcomes following an initial anti-vascular endothelial growth factor (VEGF) injection and identified factors associated with positive response.
To describe changes in treatment-naive pigment epithelial detachments associated with the initial anti-VEGF injection.
DESIGN, SETTING, AND PARTICIPANTS: Post hoc analysis of patients from the Phase III, Double-masked, Multicenter, Randomized, Active Treatment-controlled Study of the Efficacy and Safety of 0.5 mg and 2.0 mg Ranibizumab Administered Monthly or on an As-needed Basis in Patients With Subfoveal Neovascular Age-Related Macular Degeneration (HARBOR) trial (NCT00891735) with PED at baseline. The HARBOR trial was a phase 3, randomized, multicenter, double-masked, active treatment-controlled trial. Participants included treatment-naive patients with subfoveal nAMD and PEDs at baseline; intervention arms were pooled for analysis (n = 586). The HARBOR study began in July 2009 and was completed in August 2012, and the post hoc analyses were conducted between October 2016 and May 2018.
Intravitreal injections of ranibizumab, 0.5 mg and 2.0 mg, administered monthly or on an as-needed basis over 24 months.
Post hoc analyses of flattened PED frequency at month 1, univariate and multivariable analysis of patient and ocular characteristics at baseline and PED status at month 1, and total number of ranibizumab injections received stratified by PED status at month 1.
A total of 35.5% of patients (208 of 586) with PED at baseline achieved a flattened PED after a single ranibizumab injection. An additional 17.3% subsequently achieved a flattened PED at month 2. Univariate analysis identified an association between older age, lower PED height, and lower subretinal fluid thickness with PED flattening after a single injection. Multivariable analysis identified PED height as a factor associated with this anatomical outcome. Best-corrected visual acuity scores were not superior based on PED flattening at month 1. On average, patients in the as-needed arm who achieved a flattened PED after a single ranibizumab injection required fewer injections by month 24 vs patients whose PED remained present at month 1 (11.0 vs 14.2; difference, 3.3; 95% CI, 1.9-4.6; P < .001).
In this group of treatment-naive patients with PED from nAMD, after the initial ranibizumab injection approximately one-third and after the second injection approximately one-half had flattened PEDS, although visual outcomes were not superior among those that did vs did not have flattening. The findings suggest flattening may serve as a marker for less intensive as-needed injection frequencies.
ClinicalTrials.gov Identifier: NCT00891735.
色素上皮脱离(PED)是与新生血管性年龄相关性黄斑变性(nAMD)相关的常见特征,可能被认为难以治疗。因此,本研究旨在探讨初次抗血管内皮生长因子(VEGF)注射后 PED 及其视力结果的变化,并确定与阳性反应相关的因素。
描述与初次抗 VEGF 注射相关的未经治疗的色素上皮脱离的变化。
设计、地点和参与者:对来自 III 期、双盲、多中心、随机、活性治疗对照研究的患者进行事后分析,该研究评估了每月或按需给予 0.5mg 和 2.0mg 雷珠单抗治疗伴有黄斑下新生血管性年龄相关性黄斑变性(HARBOR)患者的疗效和安全性(NCT00891735),这些患者基线时存在 PED。HARBOR 试验是一项 III 期、随机、多中心、双盲、活性治疗对照试验。纳入的患者为未经治疗的伴有黄斑下 nAMD 和 PED 的患者;干预组合并进行分析(n=586)。HARBOR 研究于 2009 年 7 月开始,2012 年 8 月完成,事后分析于 2016 年 10 月至 2018 年 5 月进行。
玻璃体内注射雷珠单抗,0.5mg 和 2.0mg,每月或按需给药,持续 24 个月。
第 1 个月时 PED 平坦化的频率、第 1 个月时患者和眼部特征的单变量和多变量分析以及第 1 个月时 PED 状态的总注射次数,按第 1 个月时 PED 状态分层。
基线时有 PED 的患者(586 例中的 208 例)中,共有 35.5%在单次雷珠单抗注射后 PED 变平。另外 17.3%在第 2 个月时 PED 变平。单变量分析发现,年龄较大、PED 高度较低和视网膜下液厚度较低与单次注射后 PED 变平相关。多变量分析确定 PED 高度是与该解剖学结局相关的因素。第 1 个月 PED 变平时,最佳矫正视力评分没有提高。平均而言,在按需治疗组中,单次雷珠单抗注射后 PED 变平的患者在第 24 个月时需要的注射次数少于第 1 个月时 PED 仍存在的患者(11.0 次 vs 14.2 次;差异 3.3;95%CI,1.9-4.6;P<0.001)。
在这项来自 nAMD 的未经治疗的 PED 患者的研究中,在初次雷珠单抗注射后,大约三分之一的患者 PED 变平,在第二次注射后,大约一半的患者 PED 变平,尽管在变平的患者中视觉结果并不优于未变平的患者。这些发现表明,变平可能是减少按需注射频率的标志物。
ClinicalTrials.gov 标识符:NCT00891735。