Adaptive promising zone design for sequential parallel comparison design with continuous outcomes.

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Xinlin Lu, Guogen Shan
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引用次数: 0

Abstract

Introduction: The sequential parallel comparison design has emerged as a valuable tool in clinical trials with high placebo response rates. To further enhance its efficiency and effectiveness, adaptive strategies, such as sample size adjustment and allocation ratio modification can be employed.

Methods: We compared the performance of Jennison and Turnbull's method and the Promising Zone approach for sample size adjustment in a two-phase sequential parallel comparison design study. We also evaluated the impact of allocation ratio adjustments using Neyman and Optimal allocation strategies. Various scenarios were simulated to assess the effects of different design parameters, including weight in the test statistic, initial randomization ratio, and interim analysis timing.

Results: The Promising Zone approach demonstrated superior or comparable power to Jennison and Turnbull's method at equivalent expected sample sizes while maintaining the intuitive property that more promising interim results lead to smaller required follow-up sample sizes. However, the Promising Zone approach may require a larger maximum possible sample size in some cases. The addition of allocation ratio adjustments offered minimal improvements overall, but showed potential benefits when the variance in the treatment group was larger than that in the placebo group. We also applied our findings to a real-world example from the AVP-923 trial in patients with Alzheimer's disease-related agitation, demonstrating the practical implications of adaptive sequential parallel comparison designs in clinical research.

Discussion: Adaptive strategies can significantly enhance the efficiency of sequential parallel comparison designs. The choice between sample size adjustment methods should consider trade-offs between power, expected sample size, and maximum adjusted sample size. Although allocation ratio adjustments showed limited overall impact, they may be beneficial in specific scenarios. Future research should explore the application of these adaptive strategies to binary and survival outcomes in sequential parallel comparison designs.

连续结果序列平行比较设计的自适应前景区设计。
序贯平行比较设计在高安慰剂反应率的临床试验中已成为一种有价值的工具。为了进一步提高其效率和有效性,可以采用调整样本量和调整分配比例等自适应策略。方法:在两阶段连续平行比较设计研究中,我们比较了Jennison和Turnbull的方法和有希望区方法在样本量调整方面的性能。我们还利用内曼和最优分配策略评估了分配比例调整的影响。模拟各种情况以评估不同设计参数的影响,包括试验统计量中的权重、初始随机化比率和中期分析时间。结果:在相同的预期样本量下,有希望区域方法比Jennison和Turnbull的方法表现出优越或相当的能力,同时保持了更有希望的中期结果导致所需的后续样本量更小的直观性质。然而,在某些情况下,希望区方法可能需要更大的最大可能样本量。总的来说,增加分配比例调整提供了最小的改善,但当治疗组的差异大于安慰剂组时,显示出潜在的益处。我们还将我们的发现应用于阿尔茨海默病相关躁动患者的AVP-923试验的现实例子,证明了自适应顺序平行比较设计在临床研究中的实际意义。讨论:自适应策略可以显著提高顺序并行比较设计的效率。样本量调整方法之间的选择应该考虑功率、预期样本量和最大调整样本量之间的权衡。虽然分配比例调整的整体影响有限,但在特定情况下可能是有益的。未来的研究应该探索这些自适应策略在序列平行比较设计中的应用。
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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
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