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Design Issues in Dose-Finding Phase I Trials for Combinations of Two Agents

机译:两种药物组合的剂量寻找I期试验中的设计问题

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Combination therapy of two antitumor agents may provide treatment additivity or synergy. Phase I trials for combination therapy search for the maximum tolerated dose (MTD) for combined agents. The conventional approach is to preselect an escalation path, usually increasing the dose of one agent and then another, and to use the standard 3+3 design. However, this procedure may miss the optimum dose combination, prolong the time it takes, and increase the number of patients necessary to reach the MTD. In this study, we present strategies for a comprehensive search for MTD for a two-agent combination therapy. We evaluate algorithms based on two-stage and three-stage design as well as variations in cohort size. A two-dimensional isotonic estimation method for toxicity rate is provided. We use simulation methods to compare 2+1+3 vs. 3+3 cohort sizes. We conclude that the comprehensive search proposed in our study can be more practical and efficient in identifying the MTD in combination-therapy of two agents.
机译:两种抗肿瘤剂的联合治疗可提供治疗的加成性或协同作用。联合疗法的I期试验寻找联合药物的最大耐受剂量(MTD)。常规方法是预先选择升级路径,通常先增加一种药剂的剂量,然后再增加另一种药剂的剂量,并使用标准的3 + 3设计。但是,此过程可能会错过最佳剂量组合,从而延长所需时间,并增加达到MTD所需的患者数量。在这项研究中,我们提出了针对两种药物联合治疗的MTD的全面搜索策略。我们评估基于两阶段和三阶段设计以及同类群组大小的算法。提供了一种二维等渗估计毒性率的方法。我们使用模拟方法比较2 + 1 + 3与3 + 3同类群组的大小。我们得出的结论是,在我们的研究中提出的全面搜索可以更实用和有效地确定两种药物联合治疗中的MTD。

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