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arXiv · 2104.15086

Dose Finding Studies for Therapies with Late-Onset Toxicities: A Comparison Study of Designs

Helen Barnett·Oliver Boix·Dimintris Kontos·Thomas Jaki
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Abstract

An objective of phase I dose-finding trials is to find the maximum tolerated dose; the dose with a particular risk of toxicity. Frequently, this risk is assessed across the first cycle of therapy. However, in oncology, a course of treatment frequently consists of multiple cycles of therapy. In many cases, the overall risk of toxicity for a given treatment is not fully encapsulated by observations from the first cycle, and hence it is advantageous to include toxicity outcomes from later cycles in phase I trials. Extending the follow up period in a trial naturally extends the total length of the trial which is undesirable. We present a comparison of eight methods that incorporate late onset toxicities whilst not extensively extending the trial length. We conduct simulation studies over a number of scenarios and in two settings; the first setting with minimal stopping rules and the second setting with a full set of standard stopping rules expected in such a dose finding study. We find that the model-based approaches in general outperform the model-assisted approaches, with an Interval Censored approach and a modified version of the Time-to-Event Continual Reassessment Method giving the most promising overall performance in terms of correct selections and trial length. Further recommendations are made for the implementation of such methods.

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Helen Barnett, Oliver Boix, Dimintris Kontos, Thomas Jaki. 2021-04-30. Dose Finding Studies for Therapies with Late-Onset Toxicities: A Comparison Study of Designs. https://arxiv.org/abs/2104.15086

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