利用老年性黄斑病变治疗对比试验 (CATT) 和 IRIS® 注册表数据进行临床试验仿真的方法比较

IF 3.2 Q1 OPHTHALMOLOGY Ophthalmology science Pub Date : 2024-04-03 DOI:10.1016/j.xops.2024.100524
Helene Fevrier MPH , Andrew LaPrise BS , Michael Mbagwu MD , Theodore Leng MD, MS , Aracelis Z. Torres PhD, MPH , Durga S. Borkar MD, MMCi
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引用次数: 0

摘要

目的我们使用美国眼科学会 IRIS® 注册表(Intelligent Research in Sight)中的真实世界数据(RWD)进行精确匹配和反倾向得分加权(IPSW),以模拟 AMD 治疗比较试验(CATT)中的 2 个按月治疗组,并将 RWD 治疗组的结果与临床试验中的 2 个按月治疗组的结果进行比较。方法在2015年10月1日至2019年12月31日期间,在IRIS注册中心确定患者。在应用了CATT的所有非影像学纳入和排除标准后,仅接受贝伐珠单抗或雷尼珠单抗治疗的患者眼球被确定为符合条件的队列。根据年龄、性别和基线视力进行精确匹配和ISPW.主要结果测量通过精确匹配和IPSW生成的IRIS登记处prn治疗组基线和1年之间视力的平均变化(近似ETDRS字母).结果我们确定了427只眼睛接受了ranibizumab prn治疗,771只眼睛接受了贝伐珠单抗prn治疗。通过精确匹配,贝伐珠单抗每月治疗组中 98% 的 CATT 患者眼球(n = 281)和雷尼珠单抗每月治疗组中 87% 的 CATT 患者眼球(n = 261)与 IRIS 注册表中的患者眼球匹配。对于雷尼珠单抗按月治疗组,使用精确匹配生成的患者眼球增加了 1.9 个字母,而使用 IPSW 生成的患者眼球增加了 2.8 个字母(精确匹配:1.9 个字母 ± 14.0 vs. IPSW:2.8 个字母 ± 15.0 个字母,P = 0.43)。对于贝伐珠单抗prn 治疗臂,使用精确匹配生成的患者眼球增加了 2.4 个字母,而使用 IPSW 生成的患者眼球增加了 2.1 个字母(精确匹配:2.4 个字母 ± 15.4 vs. IPSW:2.1 个字母 ± 16.0 个字母,P = 0.79)。与之前的真实世界研究类似,与临床试验相比,IRIS注册治疗组的临床结果明显更差。
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Comparison of Methods of Clinical Trial Emulation Utilizing Data From the Comparison of AMD Treatment Trial (CATT) and the IRIS® Registry

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 (prn) 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 prn 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 prn and 771 eyes treated with bevacizumab prn. 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 prn 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, P = 0.43). For the bevacizumab prn 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, P = 0.79).

Conclusions

Both exact matching and IPSW produced similar results in emulating the prn 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 Disclosure(s)

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

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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
发文量
0
审稿时长
89 days
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