National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and University College London Institute of Ophthalmology, London, United Kingdom.
Ophthalmology. 2013 Jan;120(1):68-76. doi: 10.1016/j.ophtha.2012.07.028. Epub 2012 Sep 15.
Elevated intraocular pressure (IOP) is a major risk factor for the deterioration of open-angle glaucoma (OAG); medical IOP reduction is the standard treatment, yet no randomized placebo-controlled study of medical IOP reduction has been undertaken previously. The United Kingdom Glaucoma Treatment Study (UKGTS) tests the hypothesis that treatment with a topical prostaglandin analog, compared with placebo, reduces the frequency of visual field (VF) deterioration events in OAG patients by 50% over a 2-year period.
The UKGTS is a randomized, double-masked, placebo-controlled, multicenter treatment trial for OAG.
Five hundred sixteen newly diagnosed (previously untreated) patients with OAG were recruited prospectively at 10 centers between 2007 and 2010.
Patients were assigned by concealed telephone allocation to treatment with a prostaglandin analog (latanoprost 0.005%) or placebo. The observation period was 2 years, with subjects monitored by VF testing, quantitative imaging, optic disc photography, and tonometry at 11 visits. Data were acquired according to novel protocols optimized for the analysis of deterioration velocity. The sample size was determined for a 2-sided error of α=0.05 to detect the difference between 24% and 11% in incident deterioration over a 24-month follow-up at 90% power and assuming a 25% attrition rate.
The primary outcome was time to VF deterioration within 24 months. Secondary outcomes included the deterioration velocity of VF and quantitative imaging measures and the relationship between these velocities and risk factors for deterioration.
The study design enabled a short trial with a 2-year observation period and provided data that can be used to assess the feasibility of further shortening trial duration with the progression velocity of VF and structural imaging measurements as outcomes.
The UKGTS is the first randomized, placebo-controlled trial to evaluate the efficacy of medical treatment in reducing VF deterioration in OAG. The measurement of deterioration velocity and inclusion of quantitative imaging has the potential to reduce the number of patients and duration required for subsequent clinical trials. This trial also will quantify risk factors for deterioration, enabling more precise risk profiling of patients and the development of patient management protocols.
FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
眼内压(IOP)升高是开角型青光眼(OAG)恶化的主要危险因素;医学上降低 IOP 是标准治疗方法,但之前从未进行过降低 IOP 的医学安慰剂对照随机研究。英国青光眼治疗研究(UKGTS)检验了这样一个假设,即与安慰剂相比,用局部前列腺素类似物治疗可将 OAG 患者在 2 年内视野(VF)恶化事件的频率降低 50%。
UKGTS 是一项针对 OAG 的随机、双盲、安慰剂对照、多中心治疗试验。
2007 年至 2010 年期间,在 10 个中心前瞻性招募了 516 名新诊断(未经治疗)的 OAG 患者。
通过隐蔽电话分配,患者被分配接受前列腺素类似物(拉坦前列素 0.005%)或安慰剂治疗。观察期为 2 年,通过 VF 测试、定量成像、视盘摄影和眼压检查,在 11 次就诊时监测受试者。根据优化分析恶化速度的新方案获取数据。样本量根据双侧错误α=0.05 确定,以检测 24 个月随访期间 24%和 11%之间的差异,效能为 90%,并假设 25%的流失率。
主要结局为 24 个月内 VF 恶化的时间。次要结局包括 VF 和定量成像测量的恶化速度以及这些速度与恶化风险因素之间的关系。
该研究设计使试验时间缩短为 2 年,并提供了数据,可以用于评估以 VF 和结构成像测量的进展速度作为结果进一步缩短试验持续时间的可行性。
UKGTS 是第一项评估医学治疗降低 OAG VF 恶化效果的随机、安慰剂对照试验。恶化速度的测量和定量成像的纳入有可能减少后续临床试验所需的患者数量和时间。该试验还将量化恶化的风险因素,从而能够更精确地对患者进行风险评估,并制定患者管理方案。
作者没有与本文讨论的任何材料有关的专有或商业利益。