SearcharxivSearch

arXiv · 2511.18094

A sensitivity analysis for non-inferiority studies with non-randomised data

Abstract

Background: Non-inferiority studies based on non-randomised data are increasingly used in clinical research but remain prone to unmeasured confounding. The classical E-value offers a simple way to quantify such bias but has been applied almost exclusively with respect to the statistical null. We reformulated the E-value framework to make explicit its applicability to predefined clinical margins, thereby extending its utility to non-inferiority analyses. Development: Using the bias-factor formulation by Ding and VanderWeele, we defined the non-inferiority E-value as the minimum strength of association that an unmeasured confounder would need with both treatment and outcome, on the risk-ratio scale, to move the 95% confidence-limit estimate to the prespecified non-inferiority margin. Application: This approach was applied to three observational studies and one single-arm trial with external controls to illustrate interpretation and range. The resulting non-inferiority E-values for the confidence limits varied from about one to three, depending on design and findings. In the single-arm trial, a large gap between the confidence-limit and point-estimate NIEs reflected small sample size and wide confidence intervals, highlighting that both should be reported for a balanced assessment of robustness. Conclusion: This study reformulates the E-value to focus on clinically meaningful margins rather than the statistical null, enabling its application to non-inferiority analyses. Although the non-inferiority E-value inherits the limitations of the original method and cannot address all bias sources, it offers a transparent framework for interpreting non-randomised evidence and for generating insights that inform the design of future, more definitive randomised controlled trials.

Explore related subjects

Keep this discovery

BibTeXRIS

Daijiro Kabata, Takumi Imai. 2025-11-22. A sensitivity analysis for non-inferiority studies with non-randomised data. https://arxiv.org/abs/2511.18094

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Surprise Reduction and Nullification in Bayesian and Inverse Bayesian Inference under Ambiguous Prediction-Error Attribution

In non-stationary environments, prediction errors may signal environmental change or transient outliers, and adaptive systems must track such changes without overreacting to outliers. We distinguish surprise reduction, which updates beliefs to fit observations, from surprise nullification, which weakens constraints imposed by the predictive structure, and formalize both within Bayesian and inverse Bayesian (BIB) inference. Belief and likelihood updates are derived from variational objectives sharing a nullification strength, determined endogenously by minimizing surprise under the candidate post-update predictive distribution. In the Gaussian case, nullification expands belief and likelihood variances by a common factor relative to standard Bayesian updating, leaving the ratio unchanged. BIB thus defers attribution of the prediction error, committing to neither latent-state change nor observation-process uncertainty. The nullification strength is carried over as a candidate and is maintained or released according to the predictive surprise of the next observation. In a mean estimation task with outliers and changepoints, no scanned parameter setting of a Sage-Husa-type adaptive Kalman filter, fixed-strength BIB variant, or belief-forgetting-only variant outperforms BIB in both changepoint tracking and post-outlier stability. An oracle-informed reduced Bayesian model tracks changepoints better but is less stable after outliers. Although BIB maintains no explicit hypotheses about changepoints or outliers, it generates event-dependent dynamics. The learning rate increases after changepoints, whereas after outliers, nullification is released, and this increase is suppressed. Deferring attribution and letting subsequent observations differentiate the responses may constitute a principle of adaptive inference in non-stationary environments.

stat.ME

Generalized Ridge Refitting for the Lasso and Prediction Improvement Bounds

We study a class of Lasso based estimators obtained by applying a quadratic correction on the Lasso equicorrelation set. The penalty matrix determines both the magnitude and geometry of the correction and contains, among other cases, the isotropic Lasso--Ridge correction, least squares refitting, Gram proportional interpolation between the Lasso and least squares, and coordinate specific penalties. We first derive a closed form representation and isolate the positive gain component of the resulting prediction improvement. We then control the remaining stochastic linear term in expectation by localizing the random signed equicorrelation model around a deterministic reference support. This yields a finite sample expectation bound that explicitly accounts for the randomness induced by Lasso model selection. The resulting decomposition provides a unified framework for understanding when Lasso based quadratic corrections can improve prediction.

stat.ME

Discretization in covariate-adaptive randomization: gains and losses

Covariate-adaptive randomization(CAR) is widely implemented in clinical trials to balance prognostic covariates across treatment arms. Continuous covariates are often discretized into strata in practice, yet their consequences are not clearly understood. This paper provides a comprehensive study of the impact of discretization on both the CAR design process and the inferential results thereafter. We establish the asymptotic properties of both imbalance measures and treatment effect estimators under discretized and non-discretized settings. Practical recommendations are given on when and how discretization should be employed. We show that discretization in design is generally recommended, as it enhances robustness against model misspecification. However, if the true model is known, the most efficient strategy is to balance covariates according to that model in the design. The theoretical results are corroborated by extensive simulation studies and an empirical application to a diabetes trial dataset. Together, the results clarify the gains and losses of discretization in CAR and pave the way for learning impact of discretization to other designs and beyond.

stat.ME