Optimization of EWOC principle in BLRM design for phase 1 oncology trials.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Xiaohan Guo, Sean Kent, Arnab Maity, Wei Zhong
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引用次数: 0

Abstract

Bayesian logistic regression model (BLRM) is widely used to guide dose escalation decisions in phase 1 oncology trials. An important feature of BLRM design is the appealing safety performance due to its escalation with overdose control (EWOC). However, some recent literature indicates that BLRM with EWOC may have a relatively low probability to find the maximum tolerated dose (MTD) compared to some other dose escalation designs. This work discusses this design problem and proposes a practical solution to improve the performance of BLRM design. Specifically, we suggest increasing the EWOC cutoff from routine value 0.25 to a value between 0.3 and 0.4, which will increase the chance of finding the correct MTD with minimal compromise to overdosing risk. Our comparative simulation studies indicate that BLRM with an increased EWOC cutoff has comparable operating characteristics on the correct MTD selection and over-toxicity control as other dose escalation designs (BOIN, mTPI, keyboard, etc.). Moreover, we compare the methodology and operating characteristics of BLRM designs with various decision rules that allow more flexible overdosing control. A case study of dose escalation in a recent phase 1 oncology trial is provided to show how BLRM with optimal EWOC cutoff operates well in practice.

优化肿瘤学 1 期试验 BLRM 设计中的 EWOC 原理。
贝叶斯逻辑回归模型(BLRM)被广泛用于指导肿瘤一期试验中的剂量升级决策。贝叶斯逻辑回归模型设计的一个重要特点是通过超剂量控制(EWOC)进行剂量递增,因而具有良好的安全性。然而,最近的一些文献表明,与其他一些剂量递增设计相比,带有超剂量控制的 BLRM 找到最大耐受剂量(MTD)的概率可能相对较低。本研究讨论了这一设计问题,并提出了切实可行的解决方案,以提高 BLRM 设计的性能。具体来说,我们建议将 EWOC 临界值从常规值 0.25 提高到 0.3 至 0.4 之间,这样就能在尽量减少过量用药风险的情况下提高找到正确 MTD 的几率。我们的比较模拟研究表明,提高 EWOC 临界值的 BLRM 与其他剂量升级设计(BOIN、mTPI、键盘等)相比,在正确选择 MTD 和过量毒性控制方面具有相似的操作特性。此外,我们还比较了 BLRM 设计与各种决策规则的方法和操作特性,这些决策规则允许更灵活的超剂量控制。我们还提供了最近一项肿瘤学 1 期试验中的剂量升级案例研究,以说明具有最佳 EWOC 截止值的 BLRM 在实践中是如何运行良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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