Kiire Christine A, Morjaria Rupal, Rudenko Anna, Fantato Alexina, Smith Lewis, Smith Amy, Chong Victor
Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Clin Ophthalmol. 2015 Dec 11;9:2305-11. doi: 10.2147/OPTH.S90322. eCollection 2015.
Pegaptanib has been shown to be effective in treating diabetic macular edema (DME). In the original Phase II/III trial, however, patients with macular ischemia were excluded. In this study, we treated patients with ischemic DME.
Macular ischemia was defined as a 30% increase in the area of the foveal avascular zone (FAZ) at 45 seconds on fundus fluorescein angiography. In addition, the participants had diffuse foveal-involving DME with a central subfield thickness (CST) of >300 μm on spectral-domain optical coherence tomography. Five intravitreal pegaptanib injections were given 6 weeks apart. The final study visit was 6 weeks after the fifth injection. The primary outcome was change in the size of FAZ. Secondary outcomes were change in best-corrected visual acuity (BCVA) and the change in CST.
Thirty participants were enrolled. Three were unable to complete the full course of treatment. Their outcomes were carried forward for the first part of this analysis. There was no statistically significant change in the mean size of the FAZ from baseline to the final visit. Subclassifying participants as those with minimal/moderate ischemia (16 participants, FAZ area <1,000 pixels) and those with more severe ischemia (14 participants, FAZ area >1,000 pixels) also showed no statistically significant change in the mean area of the FAZ. On average, BCVA increased and CST decreased from baseline to the final visit, but these changes were not statistically significant. Using per protocol analysis on those participants who completed the full course of treatment, the mean BCVA increased from 49.2 to 53.9 letters (P=0.046).
In this study, intravitreal injection of pegaptanib did not significantly alter the size of the FAZ in participants with varying degrees of ischemic DME. There was, however, a significant improvement in mean BCVA in those who completed the treatment course.
已证明培加他汀尼在治疗糖尿病性黄斑水肿(DME)方面有效。然而,在最初的II/III期试验中,黄斑缺血患者被排除在外。在本研究中,我们对缺血性DME患者进行了治疗。
黄斑缺血定义为眼底荧光血管造影45秒时黄斑无血管区(FAZ)面积增加30%。此外,参与者患有累及黄斑中心凹的弥漫性DME,光谱域光学相干断层扫描显示中心子场厚度(CST)>300μm。每隔6周进行5次玻璃体内培加他汀尼注射。最后一次研究访视在第五次注射后6周。主要结局是FAZ大小的变化。次要结局是最佳矫正视力(BCVA)的变化和CST的变化。
招募了30名参与者。3人无法完成整个治疗过程。他们的结局被纳入本分析的第一部分。从基线到最后一次访视,FAZ的平均大小没有统计学上的显著变化。将参与者分为轻度/中度缺血组(16名参与者,FAZ面积<1000像素)和重度缺血组(14名参与者,FAZ面积>1000像素),FAZ的平均面积也没有统计学上的显著变化。平均而言,从基线到最后一次访视,BCVA增加,CST降低,但这些变化没有统计学意义。对完成整个治疗过程的参与者进行符合方案分析,平均BCVA从49.2提高到53.9个字母(P=0.046)。
在本研究中,玻璃体内注射培加他汀尼并未显著改变不同程度缺血性DME参与者的FAZ大小,但完成治疗过程的参与者的平均BCVA有显著改善。