Randomization-based Inference for MCP-Mod

TL;DR

This paper introduces randomization-based inference and penalized MLE methods to improve dose-response analysis in small sample phase II trials using MCP-Mod, enhancing power and accuracy especially with binary endpoints.

Contribution

It develops novel randomization-based inference techniques combined with penalized MLE to address small sample challenges in MCP-Mod dose-response analysis.

Findings

Randomization-based tests increase statistical power in small samples.

Penalized MLEs improve computational efficiency and estimation stability.

Methods maintain control over type-I error rates even with time trends.

Abstract

Dose selection is critical in pharmaceutical drug development, as it directly impacts therapeutic efficacy and patient safety of a drug. The Generalized Multiple Comparison Procedures and Modeling (MCP-Mod) approach is commonly used in Phase II trials for testing and estimation of dose-response relationships. However, its effectiveness in small sample sizes, particularly with binary endpoints, is hindered by issues like complete separation in logistic regression, leading to non-existence of estimates. Motivated by an actual clinical trial using the MCP-Mod approach, this paper introduces penalized maximum likelihood estimation (MLE) and randomization-based inference techniques to address these challenges. Randomization-based inference allows for exact finite sample inference, while population-based inference for MCP-Mod typically relies on asymptotic approximations. Simulation studies demonstrate that randomization-based tests can enhance statistical power in small to medium-sized samples while maintaining control over type-I error rates, even in the presence of time trends. Our results show that residual-based randomization tests using penalized MLEs not only improve computational efficiency but also outperform standard randomization-based methods, making them an adequate choice for dose-finding analyses within the MCP-Mod framework. Additionally, we apply these methods to pharmacometric settings, demonstrating their effectiveness in such scenarios. The results in this paper underscore the potential of randomization-based inference for the analysis of dose-finding trials, particularly in small sample contexts.