Backfilling Cohorts in Phase I Dose-Escalation Studies
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The use of `backfilling', assigning additional patients to doses deemed safe, in phase I dose-escalation studies has been used in practice to collect additional information on the safety profile, pharmacokinetics and activity of a drug. These additional patients help ensure that the Maximum Tolerated Dose (MTD) is reliably estimated and give additional information in order to determine the recommended phase II dose (RP2D). In this paper, we study the effect of employing backfilling in a phase I trial on the estimation of the MTD and the duration of the study. We consider the situation where only one cycle of follow-up is used for escalation as well as the case where there may be delayed onset toxicities. We find that, over a range of scenarios, there is an increase in the proportion of correct selections and a notable reduction in the trial duration at the cost of more patients required in the study.
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