Emulating Six Cardiovascular Outcome Trials of Antidiabetic Drugs in Individuals with Type 2 Diabetes: Analyses Based on Real-World Databases from Korea and Taiwan.

IF 5.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Hwa Yeon Ko, Philip C M Au, Michael Chun-Yuan Cheng, Ching-Lung Cheung, Ahhyung Choi, Miyuki Hsing-Chun Hsieh, Han Eol Jeong, Edward Chia-Cheng Lai, Brian Meng-Hsun Li, Kenneth K C Man, Jeremy A Rassen, Daniel Hsiang-Te Tsai, Shirley V Wang, Ian C K Wong, Ju-Young Shin, Sohee Park
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Abstract

With the increasing volume of clinical evidence derived from large-scale Asian real-world data (RWD) and the growing interest in its use in regulatory decision-making, it is important to conduct benchmarking exercises that evaluate whether studies using Asian RWD can generate similar conclusions as randomized controlled trials (RCTs). We aimed to assess whether observational studies based on Korea and Taiwan RWD can yield comparable results with trials by emulating six cardiovascular outcome trials (CVOTs) of antidiabetic drugs in individuals with type 2 diabetes (T2D). We emulated six CVOTs using nationwide claims of Korea and Taiwan. An active comparator, new-user design was applied, and observational analogues to the eligibility criteria and outcomes of the corresponding RCT were implemented. Propensity score matching was utilized to balance the treatment groups. Hazard ratios and 95% confidence intervals (CI) were estimated and compared with corresponding RCT estimates. We used three pre-specified binary agreement metrics that have been used in prior benchmarking studies to define concordance in results. Results from each of the six emulations were concordant with the corresponding CVOT on ≥ 1 binary agreement metric. Five out of six emulations indicated superiority when the corresponding CVOT only demonstrated non-inferiority. Results from emulations were more concordant with Asian-specific results from RCT, with four emulations meeting all agreement metrics. In this binational study using two Asian healthcare claims data, emulations yielded comparable clinical conclusions with the corresponding RCT, increasing the confidence in the validity of RWE studies in patients with T2D using these databases.

模拟6项2型糖尿病患者抗糖尿病药物的心血管结局试验:基于韩国和台湾真实世界数据库的分析
随着来自大规模亚洲真实世界数据(RWD)的临床证据数量的增加,以及对其在监管决策中的应用越来越感兴趣,进行基准测试来评估使用亚洲真实世界数据的研究是否可以得出与随机对照试验(rct)相似的结论是很重要的。我们的目的是评估基于韩国和台湾RWD的观察性研究是否可以通过模拟6项抗糖尿病药物在2型糖尿病(T2D)患者中的心血管结局试验(CVOTs)得出与试验相当的结果。我们使用韩国和台湾的国家主张来模拟六个cvot。采用主动比较器,新用户设计,并实施相应RCT的资格标准和结果的观察性类似物。使用倾向评分匹配来平衡治疗组。估计风险比和95%置信区间(CI),并比较相应的RCT估计值。我们使用了三个预先指定的二元一致性指标,这些指标已在先前的基准研究中使用,以定义结果的一致性。6个模拟的结果在≥1个二元一致性度量上均与相应的CVOT一致。当相应的CVOT仅显示非劣效性时,6个模拟中有5个显示了优越性。模拟的结果与RCT的亚洲特定结果更加一致,有四个模拟符合所有协议指标。在这项使用两个亚洲医疗保健索赔数据的两国研究中,模拟得出了与相应的RCT相当的临床结论,增加了使用这些数据库对T2D患者进行RWE研究的有效性的信心。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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