Edward S. Harkness Eye Institute, Columbia University College of Physicians and Surgeons, New York, New York, USA.
Retina. 2010 Oct;30(9):1368-75. doi: 10.1097/IAE.0b013e3181d50cbf.
The purpose of the study was to analyze long-term outcomes for the treatment of type 1 (subretinal pigment epithelium) neovascularization using a modified "treat and extend" antivascular endothelial growth factor dosing regimen.
We performed a retrospective, noncomparative analysis of visual acuity, funduscopic, and optical coherence tomography data for 18 eyes of 16 consecutive patients with newly diagnosed type 1 neovascularization treated with intravitreal bevaci-zumab and/or ranibizumab with at least 24-month follow-up. Three monthly injections were followed by continued treatment at intervals increasing by 2 weeks per visit to a maximum of 10 weeks. The interval was shortened if clinical or optical coherence tomography evidence of recurrent fluid at the foveola or increased extrafoveolar fluid was detected.
Median baseline logarithm of the minimum angle of resolution visual acuity was 0.53 (20/69 Snellen equivalent) and remained stable at 24 months (logarithm of the minimum angle of resolution 0.52, P = 0.84) after an average of 12 injections (range, 8-19 injections) and at 36 months (logarithm of the minimum angle of resolution 0.52, P = 0.68) after an average of 20 injections (range, 18-25 injections). Although most eyes (15 of 18 [83%]) continued to manifest extrafoveolar subretinal fluid throughout the course of treatment, only 1 eye developed geographic atrophy overlying the areas of choroidal neovascularization. During a cumulative observation period of 540 months, no eyes developed a sight-threatening submacular hemorrhage.
A modified "treat and extend" dosing regimen of intravitreal antivascular endothelial growth factor therapy reduces the need for monthly visits and imaging and allows for stable long-term visual acuity in eyes with type 1 neovascularization.
本研究旨在分析采用改良的“治疗-扩展”抗血管内皮生长因子给药方案治疗 1 型(视网膜色素上皮下)新生血管的长期疗效。
我们对 16 例连续患者的 18 只眼进行了回顾性、非对照分析,这些患者均患有新诊断的 1 型新生血管,接受了玻璃体内贝伐单抗和/或雷珠单抗治疗,随访时间至少 24 个月。前 3 个月每月注射 1 次,然后每 2 周增加 1 次治疗间隔,最多可达 10 周。如果在黄斑区或黄斑区以外发现有复发的液体或额外的黄斑区以外液体,则缩短间隔。
中位基线最小分辨角对数视力为 0.53(20/69 斯耐伦等效),在平均接受 12 次注射(范围为 8-19 次)后 24 个月(最小分辨角对数 0.52,P=0.84)和平均接受 20 次注射(范围为 18-25 次)后 36 个月(最小分辨角对数 0.52,P=0.68)时保持稳定。尽管大多数眼睛(18 只中的 15 只[83%])在整个治疗过程中仍表现出黄斑区以外的视网膜下液,但只有 1 只眼睛在脉络膜新生血管区域出现了地图样萎缩。在 540 个月的累积观察期内,没有眼睛发生威胁视力的黄斑下出血。
采用改良的“治疗-扩展”玻璃体内抗血管内皮生长因子治疗方案减少了每月就诊和影像学检查的需要,并使 1 型新生血管患者的长期视力稳定。