I 期剂量摸底试验的广义 3+3 (G3+3) 设计

Yuan Ji, Yunxuan Zhang, Andrew Liu Ji
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引用次数: 0

摘要

目的 我们提出并论证了在 I 期临床试验中采用新型无模型剂量摸底设计的可行性和可取性。方法 通用 3+3 (G3+3) 设计使用一套简单的规则,总结如下:对于一个剂量下的 3 或 6 名患者,采用 3+3 设计来决定给药剂量。对于其他人数,如果观察到的毒性率(OTR)小于 0.2,则升级到下一个较高剂量;如果 OTR 大于 0.29,则降级到下一个较低剂量;否则,保持当前剂量。结果 G3+3 设计是目前比较流行的设计(如 BOIN 和 i3+3)中唯一能复制 3+3 设计对 3 或 6 名患者的决策的设计。当治疗的患者人数不是 3 或 6 人时,G3+3 也能像其他流行设计一样产生理想的决策。计算机模拟验证了 G3+3 设计的卓越运行特性。结论 G3+3 设计推广了流行的 3+3 设计,因此可以对任何剂量下的患者人数做出理想的决策。由于 G3+3 不依赖统计模型,简单透明,无需软件工具即可实现,因此有望促进和加强现代 I 期剂量试验和早期药物开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Generalized 3+3 (G3+3) Design for Phase I Dose-Finding Trials
PURPOSE We propose and demonstrate the feasibility and desirability of a novel model-free dose-finding design for phase I clinical trials. METHODS The Generalized 3+3 (G3+3) design uses a set of simple rules summarized as follows: For 3 or 6 patients at a dose, apply the 3+3 design for making dosing decisions. For other numbers, if the observed toxicity rate (OTR) is less than 0.2, escalate to the next higher dose; if the OTR is greater than 0.29, de-escalate to the next lower dose; otherwise, stay at the current dose. RESULTS The G3+3 design is the only design that can replicate the decisions of the 3+3 design for 3 or 6 patients among the popular designs compared like BOIN and i3+3. G3+3 generates desirable decisions when the number of patients treated is not 3 or 6, like the popular designs. Computer simulation verifies the superior operating characteristics of the G3+3 design. CONCLUSION The G3+3 design generalizes the popular 3+3 design so that desirable decisions can be made for any number of patients at a dose. Since G3+3 does not rely on statistical models, is simple and transparent, and can be implemented without a software tool, it is expected to facilitate and enhance modern phase I dose-finding trials and early-phase drug development.
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