SearcharxivSearch

arXiv subjects

Stina Zetterstrom

Publications and source records attributed to Stina Zetterstrom.

2 recordsLinked to original sources

Operationalizing Allocation Probability Tests: Practical Guidance on Optimized Implementation for Power and Robustness

Recently, a new testing approach for response-adaptive clinical trials was proposed based on the allocation probabilities (AP) rather than the outcome data. While original work on the AP test focused on binary and normal endpoints and demonstrated that significant efficiency gains are possible, many critical questions remain open regarding its practical implementation and upper limits. In this work, rather than simply proposing novel statistics, we seek to understand the maximum gain that can be obtained with the AP test by optimizing how these probabilities are used to define the test statistic. We expand the method's practical utility by applying it to survival endpoints (exponential distributions) and introducing a rigorous strategy for selecting the null hypothesis to properly calibrate type I error. Our simulation studies reveal that by optimizing the functional form of the AP test, investigators can achieve a substantial increase in power, approaching the theoretical maximum, without sacrificing the patient outcome goals of the design. Furthermore, we explicitly compare the method to a standard Bayesian decision rule, finding that the optimized AP test significantly outperforms traditional frequentist tests while maintaining strict error control. This work provides a missing practical framework for implementing robust and optimized AP tests in complex response-adaptive settings.

stat.ME

SelectionBias: An R Package for Bounding Selection Bias

Selection bias can occur when subjects are included or excluded in the analysis based upon some selection criteria for the study population. The bias can jeopardize the validity of the study and sensitivity analyses for assessing the effect of the selection are desired. One method of sensitivity analysis is to construct bounds for the bias. In this work, we present an R package that can be used to calculate two previously proposed bounds for selection bias for the causal relative risk and causal risk difference for both the total and the selected population. The first bound, derived by Smith and VanderWeele (SV), is based on values of sensitivity parameters that describe parts of the joint distribution of the outcome, treatment, selection indicator and unobserved variables. The second bound is based solely on the observed data, and is therefore referred to as an assumption free (AF) bound. In addition to a tutorial for the bounds and the R package, we derive additional properties for the SV bound. We show that the sensitivity parameters are variation independent and derive feasible regions for them. Furthermore, a bound is sharp if it is a priori known that the bias can be equal to the value of the bound, given the values of the selected sensitivity parameters. Conditions for the SV bound to be sharp in the selected subpopulation are provided based on the observed data. We illustrate both the R package and the properties of the bound with a simulated dataset that emulates a study where the effect of the zika virus on microcephaly in Brazil is investigated.

stat.ME