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Frank Schaarschmidt

Publications and source records attributed to Frank Schaarschmidt.

6 recordsLinked to original sources

Prediction intervals for overdispersed multinomial data with application to historical controls

In pharmaceutical and toxicological research, historical control data are increasingly used to validate concurrent control groups, typically via the construction of historical control limits. While methods have been described for continuous and dichotomous endpoints, approaches for overdispersed multinomial data, common in developmental and reproductive toxicology or histopathology, are currently lacking. This article introduces and compares methods for constructing simultaneous prediction intervals for future multinomial observations subject to overdispersion. We investigate a range of frequentist approaches, including asymptotic approximations and bootstrap techniques (incorporating symmetric, asymmetric, and marginal calibration, as well as rank-based methods), alongside Bayesian hierarchical models. Extensive simulation studies assessing simultaneous coverage probability and the balance of lower and upper tail error probabilities show that standard asymptotic methods and simple Bonferroni adjustments yield liberal intervals, especially for small sample sizes or rare event categories. In contrast, bootstrap methods, specifically the Marginal Calibration and Rank-Based Simultaneous Confidence Sets, provide reliable error control and equal tail probabilities across diverse scenarios involving varying cluster sizes and degrees of overdispersion. These methods fill an important gap for multinomial endpoints and support the validation of concurrent controls using historical control data, in line with the recent European Food Safety Authority scientific opinion on the use and reporting of historical control data.

stat.ME

Including historical control data in simultaneous inference for pre-clinical multi-arm studies

In pre- and non-clinical toxicology, the reduction of animal use is highly desireable. Although approaches for possible sample size reduction in the concurrent control group were suggested previously under the virtual control groups framework for continuous endpoints, methodology that is applicable to binary outcomes that occur in long-term carcinogenicity studies is currently missing. In order to augment animals in the current control group with historical control data, we propose approaches that rely on dynamic Bayesian borrowing and simultaneous credible intervals for risk ratios. Several operation characteristics such as familywise error rate (FWER) and power are assessed via Monte-Carlo simulations and compared to the ones of approaches that rely on pooling of historical and current observations. It turned out that under optimal conditions, Bayesian approaches based on robustified prior distributions enable a substantial reduction of the control groups sample size, while still controlling the FWER up to a satisfactory level. Furthermore, at least to some extend, these approaches were able to protect against possible drift. This hightlights the potential of Bayesian study designs to reduce animal use in toxicology through re-use of the large pool of existing control data.

stat.ME

A versatile trend test for the evaluation of tumor incidences in long-term carcinogenicity bioassays

For the evaluation of carcinogenicity bioassays a new trend test is proposed which is based on a maximum of arithmetic, ordinal, and logarithmic regression scores as well as the Williams-type contrasts for either crude proportions or more appropriate poly3-estimates for the tumor-by-time relationships. This test provides an almost appropriate power for most shapes of dose-response relationships (including for possible downturn effect at high(er) dose(s)), common signs of significance (p-value, confidence limits) and the information on the probable shape. Related software is easily available within the CRAN-packages tukeytrend, MCPAN, multcomp.

stat.AP

Model-based simultaneous inference for multiple subgroups and multiple endpoints

Various methodological options exist on evaluating differences in both subgroups and the overall population. Most desirable is the simultaneous study of multiple endpoints in several populations. We investigate a newer method using multiple marginal models (mmm) which allows flexible handling of multiple endpoints, including continuous, binary or time-to-event data. This paper explores the performance of mmm in contrast to the standard Bonferroni approach via simulation. Mainly these methods are compared on the basis of their familywise error rate and power under different scenarios, varying in sample size and standard deviation. Additionally, it is shown that the method can deal with overlapping subgroup definitions and different combinations of endpoints may be assumed. The reanalysis of a clinical example shows a practical application.

stat.AP

A Tukey type trend test for repeated carcinogenicity bioassays, motivated by multiple glyphosate studies

In the last two decades, significant methodological progress to the simultaneous inference of simple and complex randomized designs, particularly proportions as endpoints, occurred. This includes: i) the new Tukey trend test approach, ii) multiple contrast tests for binomial proportions, iii) multiple contrast tests for poly-k estimates, and Add-1 approximation for one-sided inference. This report focus on a new Tukey type trend test to evaluate repeated long-term carcinogenicity bioassays which was motivated by multiple glyphosate studies. Notice, it is not the aim here to contribute to the evaluation of Glyphosate and its controversies. By means of the CRAN-packages tukeytrend, MCPAN, multcomp the real data analysis is straightforward possible.

stat.ME

A modified Armitage test for more than a linear trend on proportions

The Armitage test for linear trend in proportions can be modified using the multiple marginal model approach for three regression models with arithmetic, ordinal and logarithmic dose scores simultaneously, to be powerful against a wide range of possible dose response relationships. Moreover, it can be used for particular designs in the generalized linear (mixed) model for the three common effect sizes odds ratio, risk ratio and risk difference. The related R package tukeytrend allows simple generalizations, e.g. the analysis 2-by-k table data with a possible plateau shape or analysing overdispersed proportions. The evaluation of further real data examples are available in a vignette to that R package.

stat.ME