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Max Menssen

Publications and source records attributed to Max Menssen.

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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

Prediction intervals for overdispersed binomial endpoints and their application to toxicological historical control data

For toxicology studies, the validation of the concurrent control group by historical control data (HCD) has become requirements. This validation is usually done by historical control limits (HCL), which should cover the observations of the concurrent control with a predefined level of confidence. In many applications, HCL are applied to dichotomous data, e.g. the number of rats with a tumor vs. the number of rats without a tumor (carcinogenicity studies) or the number of cells with a micronucleus out of a total number of cells. Dichotomous HCD may be overdispersed and can be heavily right- (or left-) skewed, which is usually not taken into account in the practical applications of HCL. To overcome this problem, four different prediction intervals (two frequentist, two Bayesian), that can be applied to such data, are proposed. Based on comprehensive Monte-Carlo simulations, the coverage probabilities of the proposed prediction intervals were compared to heuristical HCL typically used in daily toxicological routine (historical range, limits of the np-chart, mean plus minus 2 SD). Our simulations reveal, that frequentist bootstrap calibrated prediction intervals control the type-1-error best, but, also prediction intervals calculated based on Bayesian generalized linear mixed models appear to be practically applicable. Contrary, all heuristics fail to control the type-1-error. The application of HCL is demonstrated based on a real life data set containing historical controls from long-term carcinogenicity studies run on behalf of the U.S. National Toxicology Program. The proposed frequentist prediction intervals are publicly available from the R package predint, whereas R code for the computation of the two Bayesian prediction intervals is provided via GitHub.

stat.AP

Prediction intervals for overdispersed Poisson data and their application in medical and pre-clinical quality control

In pre-clinical and medical quality control, it is of interest to assess the stability of the process under monitoring or to validate a current observation using historical control data. Classically, this is done by the application of historical control limits (HCL) graphically displayed in control charts. In many applications, HCL are applied to count data, e.g. the number of revertant colonies (Ames assay) or the number of relapses per multiple sclerosis patient. Count data may be overdispersed, can be heavily right-skewed and clusters may differ in cluster size or other baseline quantities (e.g. number of petri dishes per control group or different length of monitoring times per patient). Based on the quasi-Poisson assumption or the negative-binomial distribution, we propose prediction intervals for overdispersed count data to be used as HCL. Variable baseline quantities are accounted for by offsets. Furthermore, we provide a bootstrap calibration algorithm that accounts for the skewed distribution and achieves equal tail probabilities. Comprehensive Monte-Carlo simulations assessing the coverage probabilities of eight different methods for HCL calculation reveal, that the bootstrap calibrated prediction intervals control the type-1-error best. Heuristics traditionally used in control charts (e.g. the limits in Sheward c- or u-charts or the mean plus minus 2 SD) fail to control a pre-specified coverage probability. The application of HCL is demonstrated based on data from the Ames assay and for numbers of relapses of multiple sclerosis patients. The proposed prediction intervals and the algorithm for bootstrap calibration are publicly available via the R package predint.

stat.AP

The R package predint: Prediction intervals for overdispersed binomial and Poisson data or based on linear random effects models in R

A prediction interval is a statistical interval that should encompass one (or more) future observation(s) with a given coverage probability and is usually computed based on historical control data. The application of prediction intervals is discussed in many fields of research, such as toxicology, pre-clinical statistics, engineering, assay validation or for the assessment of replication studies. Anyhow, the prediction intervals implemented in predint descent from previous work that was done in the context of toxicology and pre-clinical applications. Hence the implemented methodology reflects the data structures that are common in these fields of research. In toxicology the historical data is often comprised of dichotomous or counted endpoints. Hence it seems natural to model these kind of data based on the binomial or the Poisson distribution. Anyhow, the historical control data is usually comprised of several studies. These clustering gives rise to possible overdispersion which has to be reflected for interval calculation. In pre-clinical statistics, the endpoints are often assumed to be normal distributed, but usually are not independent from each other due to the experimental design (cross-classified and/or hierarchical structures). These dependencies can be modeled based on linear random effects models. Hence, predint provides functions for the calculation of prediction intervals and one-sided bounds for overdispersed binomial data, for overdispersed Poisson data and for data that is modeled by linear random effects models.

stat.AP