导航儿科试验实施中的挑战:将贝叶斯序列设计与处理主要和次要终点的半参数启发相结合。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Danila Azzolina, Ileana Baldi, Silvia Bressan, Mohd Rashid Khan, Liviana Da Dalt, Dario Gregori, Paola Berchialla
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引用次数: 0

摘要

背景:本研究提出了一种贝叶斯自适应半参数方法,旨在解决儿科随机对照试验(rct)的挑战。该研究的重点是有效地处理主要和次要终点,这是儿科试验中经常被忽视的一个关键方面。这种方法特别适用于存在稀疏或相互冲突的先前数据的情况,这在儿科研究中很常见,特别是对于罕见疾病或病症。方法:我们的方法考虑贝叶斯自适应设计,增强了b样条半参数先验,允许随着持续数据动态更新先验。这提高了治疗效果估计的效率和准确性。半参数先验固有的灵活性使其适用于儿科人群,其中对治疗的反应可能是高度可变的。设计手术特征通过模拟研究进行评估,模拟研究的动机是肾脏瘢痕性尿路感染试验(RESCUE)的真实案例。结果:我们证明,即使出现招募挑战、不确定性和先验数据冲突,半参数先验参数化在研究结论中也表现出正确声明治疗效果的改进趋势。此外,半参数先验设计证明了真正无用停止的能力,这种趋势随着样本量和中断率的变化而变化。基于参数先验的方法在中期评估中检测治疗效果更有效,特别是在样本量较大的情况下。结论:我们的研究结果表明,这些方法在处理儿科试验的复杂性方面特别有效,在这些试验中,先前的数据可能有限或相互矛盾。半参数先验设计在纳入新证据方面的灵活性在解决招聘挑战和在有限数据下做出明智决策方面是有利的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating challenges in pediatric trial conduct: integrating bayesian sequential design with semiparametric elicitation for handling primary and secondary endpoints.

Background: This study presents a Bayesian Adaptive Semiparametric approach designed to address the challenges of pediatric randomized controlled trials (RCTs). The study focuses on efficiently handling primary and secondary endpoints, a critical aspect often overlooked in pediatric trials. This methodology is particularly pertinent in scenarios where sparse or conflicting prior data are present, a common occurrence in pediatric research, particularly for rare diseases or conditions.

Method: Our approach considers Bayesian adaptive design, enhanced with B-Spline Semiparametric priors, allowing for the dynamic updating of priors with ongoing data. This improves the efficiency and accuracy of the treatment effect estimation. The Semiparametric prior inherent flexibility makes it suitable for pediatric populations, where responses to treatment can be highly variable. The design operative characteristics were assessed through a simulation study, motivated by the real-world case of the REnal SCarring Urinary infEction Trial (RESCUE).

Result: We demonstrate that Semiparametric prior parametrization exhibits an improved tendency to correctly declare the treatment effect at the study conclusion, even if recruitment challenges, uncertainty, and prior-data conflict arise. Moreover, the Semiparametric prior design demonstrates an improved ability in truly stopping for futility, with this tendency varying with the sample size and discontinuation rates. Approaches based on Parametric priors are more effective in detecting treatment efficacy during interim assessments, particularly with larger sample sizes.

Conclusion: Our findings indicate that these methods are especially effective in managing the complexities of pediatric trials, where prior data may be limited or contradictory. The flexibility of Semiparametric prior design in incorporating new evidence proves advantageous in addressing recruitment challenges and making informed decisions with restricted data.

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来源期刊
BMC Medical Research Methodology
BMC Medical Research Methodology 医学-卫生保健
CiteScore
6.50
自引率
2.50%
发文量
298
审稿时长
3-8 weeks
期刊介绍: BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.
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