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首页> 外文期刊>Journal of Personalized Medicine >Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
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Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials

机译:支持在随机对照试验中纳入药物遗传学生物标志物的证据

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Pharmacogenetics and biomarkers are becoming normalised as important technologies to improve drug efficacy rates, reduce the incidence of adverse drug reactions, and make informed choices for targeted therapies. However, their wider clinical implementation has been limited by a lack of robust evidence. Suitable evidence is required before a biomarker’s clinical use, and also before its use in a clinical trial. We have undertaken a review of five pharmacogenetic biomarker-guided randomised controlled trials (RCTs) and evaluated the evidence used by these trials to justify biomarker inclusion. We assessed and quantified the evidence cited in published rationale papers, or where these were not available, obtained protocols from trial authors. Very different levels of evidence were provided by the trials. We used these observations to write recommendations for future justifications of biomarker use in RCTs and encourage regulatory authorities to write clear guidelines.
机译:药物遗传学和生物标志物已被标准化为重要技术,可提高药物功效率,减少药物不良反应的发生率并为靶向疗法做出明智的选择。然而,由于缺乏可靠的证据,其更广泛的临床应用受到了限制。在生物标志物临床使用之前以及在临床试验中使用之前,都需要适当的证据。我们对5项药物遗传学生物标志物指导的随机对照试验(RCT)进行了综述,并评估了这些试验所使用的证据来证明生物标志物的合理性。我们评估并量化了已发表的基本原理论文中引用的证据,或在没有这些依据的情况下,从试验作者处获得了方案。试验提供的证据水平差异很大。我们使用这些观察结果为将来在RCT中使用生物标志物的理由撰写了建议,并鼓励监管机构编写明确的指南。

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