Smith Bradley T, Dhalla Mandeep S, Shah Gaurav K, Blinder Kevin J, Ryan Edwin H, Mittra Robert A
Barnes Retina Institute, St. Louis, Missouri, USA.
Retina. 2008 May;28(5):675-81. doi: 10.1097/IAE.0b013e31816b316e.
To report the outcome for eyes treated with intravitreal injection of bevacizumab combined with verteporfin photodynamic therapy (PDT) for choroidal neovascularization (CNV) in age-related macular degeneration (AMD).
Interventional, consecutive, retrospective case series including 40 eyes of 40 patients with newly diagnosed juxtafoveal or subfoveal CNV secondary to AMD.
The charts of patients treated with a 1.25-mg intravitreal injection of bevacizumab followed by PDT within a 2-week period were reviewed. Main outcome measures were visual acuity stabilization (defined as no change or a gain in visual acuity) and need for retreatment.
Thirty-three (83%) of 40 eyes had stabilization of visual acuity. Mean improvement in visual acuity was 1.73 lines. Twenty-six eyes (65%) required only a single intravitreal injection of bevacizumab combined with PDT. Of the 23 eyes with 12 months of follow-up, 17 (74%) had stabilization of visual acuity, while 9 (40%) had improvement in visual acuity (mean, 1.22 Snellen lines). Eleven eyes (48%) required only a single combined treatment for CNV resolution at the 12-month follow-up. Fifteen (88%) of 17 eyes with only 6 months of follow-up required only a single combined treatment. There were no complications such as endophthalmitis, uveitis, or ocular hypertension.
These findings suggest that eyes treated with both intravitreal injection of bevacizumab and PDT require none to a minimal number of re-treatments to have stabilization of vision, even at 12 months of follow-up. Further investigation with large controlled trials is warranted to outline the appropriate treatment paradigm for combination therapy.
报告玻璃体内注射贝伐单抗联合维替泊芬光动力疗法(PDT)治疗年龄相关性黄斑变性(AMD)脉络膜新生血管(CNV)的眼部治疗结果。
干预性、连续性、回顾性病例系列,包括40例新诊断的继发于AMD的近黄斑中心凹或黄斑中心凹下CNV患者的40只眼。
回顾了在2周内接受1.25mg玻璃体内注射贝伐单抗随后进行PDT治疗的患者病历。主要观察指标为视力稳定(定义为视力无变化或提高)及再次治疗需求。
40只眼中的33只(83%)视力稳定。视力平均提高1.73行。26只眼(65%)仅需单次玻璃体内注射贝伐单抗联合PDT。在随访12个月的23只眼中,17只(74%)视力稳定,而9只(40%)视力提高(平均1.22 Snellen行)。在12个月随访时,11只眼(48%)仅需单次联合治疗即可使CNV消退。在仅随访6个月的17只眼中,15只(88%)仅需单次联合治疗。未出现眼内炎、葡萄膜炎或高眼压等并发症。
这些结果表明,即使在随访12个月时,接受玻璃体内注射贝伐单抗和PDT治疗的眼也无需或仅需极少次数的再次治疗即可实现视力稳定。有必要通过大型对照试验进行进一步研究,以明确联合治疗的合适治疗模式。