Ivanova Anastasia, Wang Kai
Department of Biostatistics, CB #7420, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Stat Med. 2004 Jun 30;23(12):1861-70. doi: 10.1002/sim.1796.
This paper investigates the design and analysis of dose-finding trials with two agents. The set of doses for each agent is fixed in advance. The goal of the trial is to find the set of dose combinations with probability of toxicity closest to a pre-specified value. For each of the two agents we assume that the probability of toxicity of an agent is non-decreasing with dose when the dose of the other agent is fixed. Using this assumption we construct a new non-parametric design that operates on a two-dimensional grid of all possible dose combinations. A bivariate isotonic regression estimator of the maximum tolerated combinations is described. We conclude that the new design and the bivariate isotonic estimator are superior to the procedure where several independent dose-finding trials are run.
本文研究了使用两种药物的剂量探索试验的设计与分析。每种药物的剂量组在试验前已确定。试验的目标是找到毒性概率最接近预先指定值的剂量组合集。对于两种药物中的每一种,我们假设当另一种药物的剂量固定时,该药物的毒性概率随剂量非递减。基于此假设,我们构建了一种新的非参数设计,该设计在所有可能剂量组合的二维网格上进行操作。文中描述了最大耐受组合的双变量保序回归估计量。我们得出结论,新设计和双变量保序估计量优于进行多个独立剂量探索试验的方法。