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地理萎缩治疗试验的设计特征:对ClinicalTrials.gov中注册试验的系统评价

Design Characteristics of Geographic Atrophy Treatment Trials: Systematic Review of Registered Trials in ClinicalTrials.gov.

作者信息

Cheng Qianqian Ellie, Gao Jeffrey, Kim Benjamin J, Ying Gui-Shuang

机构信息

School of Arts and Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.

Conestoga High School, Berwyn, Pennsylvania.

出版信息

Ophthalmol Retina. 2018 Jun;2(6):518-525. doi: 10.1016/j.oret.2017.08.018. Epub 2017 Nov 9.

Abstract

PURPOSE

Currently there is no effective treatment for geographic atrophy (GA) secondary to age-related macular degeneration, despite many trials that were completed or are ongoing. The purpose of this systematic review is to describe the key design characteristics of GA trials. Well-designed GA trials using appropriate outcome measures are critical for the discovery of an effective treatment. This review may provide valuable insights for improving the design of future trials.

METHODS

Two reviewers independently searched for eligible trials (last search on February 28, 2017) and abstracted data of design characteristics including eligibility criteria, sample size, length of follow-up, and primary and secondary outcomes.

RESULTS

Among 53 registered GA treatment trials, 10 (19%) were in phase 1, 36 (68%) in phase 1-2 or 2 (phase 2), and 7 (13%) in phase 2-3 or 3 (phase 3); 24 of the 53 trials (45%) are ongoing. The most common interventions were anti-inflammatory agents (40%). GA growth was used as the primary outcome in 58% of phase 2 trials and 71% of phase 3 trials, and as a secondary outcome in 31% of phase 2 trials and 0% of phase 3 trials. Visual acuity (VA) was used as the primary outcome in 17% of phase 2 trials and 14% of phase 3 trials, and as a secondary outcome in 67% of phase 2 trials and 57% of phase 3 trials. The median sample size of trials was 22 in phase 1, 60 in phase 2, and 772 in phase 3, with median follow-up length of 0.7, 1.0, and 2.0 years, respectively. The study eye baseline VA criterion was specified in 33 trials (62%) and varied across trials, with a lower limit of 20/50 to 20/400. The criterion for baseline GA size was specified in 14 trials (26%), with minimum GA size 0.5 to 1 disc area.

CONCLUSIONS

There exists large variation in the design characteristics of GA treatment trials. GA growth is the most common primary outcome measure, and VA is the most common secondary outcome measure. Future trials should consider these design characteristics to advance the discovery of an effective treatment for GA.

摘要

目的

尽管已经完成或正在进行许多试验,但目前尚无针对年龄相关性黄斑变性继发的地图样萎缩(GA)的有效治疗方法。本系统评价的目的是描述GA试验的关键设计特征。采用适当结局指标进行精心设计的GA试验对于发现有效治疗方法至关重要。本评价可能为改进未来试验的设计提供有价值的见解。

方法

两名研究者独立检索符合条件的试验(最后检索时间为2017年2月28日),并提取设计特征数据,包括纳入标准、样本量、随访时间以及主要和次要结局。

结果

在53项已注册的GA治疗试验中,10项(19%)处于1期,36项(68%)处于1-​2期或2期,7项(13%)处于2-​3期或3期;53项试验中有24项(45%)正在进行。最常见的干预措施是抗炎药(40%)。在58%的2期试验和71%的3期试验中,GA面积扩大被用作主要结局,在31%的2期试验和0%的3期试验中被用作次要结局。在17%的2期试验和14%的3期试验中,视力(VA)被用作主要结局,在67%的2期试验和57%的3期试验中被用作次要结局。各期试验的样本量中位数分别为:1期22例,2期60例,3期772例,随访时间中位数分别为0.7年、1.0年和2.0年。33项试验(62%)明确了研究眼的基线视力标准,各试验标准不同,下限为20/50至20/400。14项试验(26%)明确了基线GA面积标准,最小GA面积为0.5至1个视盘面积。

结论

GA治疗试验的设计特征存在很大差异。GA面积扩大是最常见的主要结局指标,VA是最常见的次要结局指标。未来的试验应考虑这些设计特征,以推动GA有效治疗方法的发现。

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