Estimation and expected sample size in Simon's two-stage designs that stop as early as possible

Publication date

2022-09-01

Authors

Daletzakis, Antonios
van den Bor, R.M.
Jonker, Marianne A
Roes, Kit C BORCID 0000-0002-6775-1963ISNI 0000000040154793
van Tinteren, Harm

Editors

Advisors

Supervisors

Document Type

Article

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License

taverne

Abstract

In early phase clinical studies in oncology, Simon's two-stage designs are widely used. The trial design could be made more efficient by stopping early in the second stage when the required number of responses is reached, or when it has become clear that this target can no longer be met (a form of non-stochastic curtailment). Early stopping, however, will affect proper estimation of the response rate. We propose a uniformly minimum-variance unbiased estimator (UMVUE) for the response rate in this setting. The estimator is proven to be UMVUE using the Rao-Blackwell theorem. We evaluate the estimator's properties in terms of bias and mean squared error, both analytically and via simulations. We derive confidence intervals based on sample space orderings, and assess the coverage. For various design options, we evaluate the reduction in expected sample size as a function of the true response rate. Our method provides a solution for estimating response rates in case of a non-stochastic curtailment Simon's two-stage design.

Keywords

early stopping, expected sample size reduction, non-stochastic curtailment, response rate estimation, sequential designs, two-stage design, Taverne, Statistics and Probability, Pharmacology, Pharmacology (medical)

Citation

Daletzakis, A, van den Bor, R, Jonker, M A, Roes, K C B & van Tinteren, H 2022, 'Estimation and expected sample size in Simon's two-stage designs that stop as early as possible', Pharmaceutical Statistics, vol. 21, no. 5, pp. 879-894. https://doi.org/10.1002/pst.2200