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利用年龄相关性黄斑变性治疗试验(CATT)和IRIS®注册中心的数据进行临床试验模拟方法的比较

Comparison of Methods of Clinical Trial Emulation Utilizing Data From the Comparison of AMD Treatment Trial (CATT) and the IRIS® Registry.

作者信息

Fevrier Helene, LaPrise Andrew, Mbagwu Michael, Leng Theodore, Torres Aracelis Z, Borkar Durga S

机构信息

Verana Health, San Francisco, California.

Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, California.

出版信息

Ophthalmol Sci. 2024 Apr 3;4(5):100524. doi: 10.1016/j.xops.2024.100524. eCollection 2024 Sep-Oct.

Abstract

PURPOSE

We used exact matching and inverse propensity score weighting (IPSW) using real-world data (RWD) from the American Academy of Ophthalmology IRIS® Registry (Intelligent Research in Sight) to emulate the 2 pro re nata () treatment arms from the Comparison of AMD Treatment Trial (CATT) and to compare the outcomes of the RWD arms to the 2 monthly treatment arms from the clinical trial.

DESIGN

Retrospective cohort study utilizing deidentified electronic health record registry data and patient-level deidentified clinical trial data.

SUBJECTS

All treatment-naive patient eyes with neovascular age-related macular degeneration treated with ranibizumab or bevacizumab only for 1 year from either the CATT or the IRIS Registry.

METHODS

Patients were identified in the IRIS Registry between October 1, 2015 and December 31, 2019. After all nonimaging-based inclusion and exclusion criteria from the CATT were applied, patient eyes receiving bevacizumab or ranibizumab only on a basis were identified as the eligible cohort. Exact matching and ISPW was applied based on age, gender, and baseline visual acuity.

MAIN OUTCOME MEASURES

Mean change in visual acuity, in approximated ETDRS letters, between baseline and 1 year for the IRIS Registry prn treatment arms generated by exact matching and IPSW.

RESULTS

We identified 427 eyes treated with ranibizumab and 771 eyes treated with bevacizumab . Using exact matching, 98% (n = 281) of CATT patient eyes in the bevacizumab monthly treatment arm and 87% (n = 261) of CATT patient eyes in the ranibizumab monthly treatment arm were matched to a patient eye in the IRIS Registry. For the ranibizumab treatment arm, patient eyes generated using exact matching gained 1.9 letters and those generated using IPSW gained 2.8 letters (exact matching: 1.9 letters ± 14.0 vs. IPSW: 2.8 letters ± 15.0 letters,  = 0.43). For the bevacizumab treatment arm, patient eyes generated using exact matching gained 2.4 letters and those generated using IPSW gained 2.1 letters (exact matching: 2.4 letters ± 15.4 vs. IPSW: 2.1 letters ± 16.0 letters,  = 0.79).

CONCLUSIONS

Both exact matching and IPSW produced similar results in emulating the treatment arms of the CATT using IRIS Registry data and patient-level clinical trial data. Similar to prior real-world studies, the clinical outcomes were significantly worse in the IRIS Registry treatment arms compared with the clinical trial.

FINANCIAL DISCLOSURES

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

我们使用美国眼科学会IRIS®注册库(视力智能研究)的真实世界数据(RWD)进行精确匹配和逆倾向评分加权(IPSW),以模拟年龄相关性黄斑变性治疗试验(CATT)中的2个按需治疗(pro re nata,prn)治疗组,并将RWD组的结果与该临床试验中的2个每月治疗组进行比较。

设计

利用去识别化的电子健康记录注册库数据和患者水平的去识别化临床试验数据进行回顾性队列研究。

研究对象

所有初治的新生血管性年龄相关性黄斑变性患者眼,仅接受雷珠单抗或贝伐单抗治疗1年,数据来自CATT或IRIS注册库。

方法

在IRIS注册库中识别出2015年10月1日至2019年12月31日期间的患者。应用CATT中所有基于非影像学的纳入和排除标准后,将仅按需接受贝伐单抗或雷珠单抗治疗的患者眼确定为合格队列。基于年龄、性别和基线视力进行精确匹配和IPSW。

主要观察指标

通过精确匹配和IPSW生成的IRIS注册库prn治疗组在基线和1年之间以近似ETDRS字母表示的视力平均变化。

结果

我们识别出427只接受雷珠单抗治疗的眼和771只接受贝伐单抗治疗的眼。使用精确匹配,贝伐单抗每月治疗组中98%(n = 281)的CATT患者眼和雷珠单抗每月治疗组中87%(n = 261)的CATT患者眼与IRIS注册库中的患者眼匹配。对于雷珠单抗治疗组,使用精确匹配生成的患者眼视力提高了1.9个字母,使用IPSW生成的患者眼视力提高了2.8个字母(精确匹配:1.9个字母±14.0,IPSW:2.8个字母±15.0个字母,P = 0.43)。对于贝伐单抗治疗组,使用精确匹配生成的患者眼视力提高了2.4个字母,使用IPSW生成的患者眼视力提高了2.1个字母(精确匹配:2.4个字母±15.4,IPSW:2.1个字母±16.0个字母,P = 0.79)。

结论

使用IRIS注册库数据和患者水平的临床试验数据,精确匹配和IPSW在模拟CATT的治疗组方面产生了相似的结果。与先前的真实世界研究相似,IRIS注册库治疗组的临床结果与临床试验相比明显更差。

财务披露

本文末尾的脚注和披露中可能会有专有或商业披露信息。

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