4.5 Article Proceedings Paper

Dose-finding approach for dose escalation with overdose control considering incomplete observations

期刊

STATISTICS IN MEDICINE
卷 30, 期 13, 页码 1584-1594

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WILEY-BLACKWELL
DOI: 10.1002/sim.4128

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dose-finding study; phase I trial; escalation with overdose control; time-to-event; trial duration

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We propose a hybrid design, the time-to-event dose-escalation method with overdose control (TITE-EWOC), introducing the time-to-event approach, developed by Cheung et al., in the EWOC method, developed by Babb et al. The aim of this new design is to decrease the dose-finding trial duration, without impairing the characteristics of the EWOC design, especially the overdose control ability. We conducted a simulation study, exploring four dose-toxicity relationships and three mean inter-patient arrival times. Performances of TITE-EWOC were compared with those of the EWOC method. This study shows that the trial duration can be greatly decreased with the TITE-EWOC, without impacting the proportion of overdosed patients or the number of dose-limiting toxicities by trial, for all explored dose-toxicity relationships, except for very short inter-patient arrival times. The ability of the method to find the true maximum tolerated dose remains unchanged. Copyright (C) 2011 John Wiley & Sons, Ltd.

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