Afternoon discussion: Statistical issues in clinical trials conference on dose finding

The adoption of innovative, model-based, and computationally intensive clinical trial designs is challenged by barriers including clinician engagement, regulatory acceptance, dissemination beyond major research institutions, and patient accrual. This session explored strategies to overcome these barriers. Key approaches discussed included the development of user-friendly software and interactive platforms to enhance transparency, open sharing of algorithms, and recognition of software contributions in academic publishing. Building collaborations with stakeholders predisposed to innovation, fostering interdisciplinary communication, and producing complementary methodological and clinical publications were emphasized as essential steps. Practical considerations for trials with small sample sizes included the use of adaptive designs, individualized trials, and alternative optimization strategies when traditional theoretical assumptions are infeasible. A major theme of the discussion was the importance of model assumptions in innovative designs. Questions were raised about the sensitivity of results to these assumptions and the robustness of methods, particularly under limited sample sizes. Addressing this requires extensive simulation studies across varied scenarios to assess operating characteristics. The focus should be on achieving clinically meaningful goals-such as identifying effective dose regions-rather than perfect model specification. Speakers emphasized the need to acknowledge and, when feasible, test assumptions post hoc, integrating such verification as secondary objectives in trial design. An iterative scientific process was encouraged, recognizing that trials not only serve immediate clinical goals but also advance broader scientific understanding. Assumptions provide a principled foundation for methodology, but thoughtful scrutiny of their realism was urged, given the risk of relying on overly strong or untestable premises. The potential of metaheuristic algorithms was highlighted for efficiently identifying optimal designs across different model assumptions, supporting robustness evaluations. Practical implementation should adapt optimal designs to stakeholder needs while preserving acceptable statistical efficiency. In sum, advancing the adoption of innovative designs requires improved communication, infrastructure, and methodological transparency, alongside careful evaluation of model assumptions and robustness.

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Publication Details

Journal
Clinical Trials
Published
2025-06-27
DOI
https://doi.org/10.1177/17407745251350598
Primary Topic
Statistical Methods in Clinical Trials
Type
article
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article

Afternoon discussion: Statistical issues in clinical trials conference on dose finding

Anna Heath, Kelley M. Kidwell
Clinical Trials
Statistical Methods in Clinical Trials
article

Afternoon discussion: Statistical issues in clinical trials conference on dose finding

Anna Heath, Kelley M. Kidwell
article en

Abstract

The adoption of innovative, model-based, and computationally intensive clinical trial designs is challenged by barriers including clinician engagement, regulatory acceptance, dissemination beyond major research institutions, and patient accrual. This session explored strategies to overcome these barriers. Key approaches discussed included the development of user-friendly software and interactive platforms to enhance transparency, open sharing of algorithms, and recognition of software contributions in academic publishing. Building collaborations with stakeholders predisposed to innovation, fostering interdisciplinary communication, and producing complementary methodological and clinical publications were emphasized as essential steps. Practical considerations for trials with small sample sizes included the use of adaptive designs, individualized trials, and alternative optimization strategies when traditional theoretical assumptions are infeasible. A major theme of the discussion was the importance of model assumptions in innovative designs. Questions were raised about the sensitivity of results to these assumptions and the robustness of methods, particularly under limited sample sizes. Addressing this requires extensive simulation studies across varied scenarios to assess operating characteristics. The focus should be on achieving clinically meaningful goals-such as identifying effective dose regions-rather than perfect model specification. Speakers emphasized the need to acknowledge and, when feasible, test assumptions post hoc, integrating such verification as secondary objectives in trial design. An iterative scientific process was encouraged, recognizing that trials not only serve immediate clinical goals but also advance broader scientific understanding. Assumptions provide a principled foundation for methodology, but thoughtful scrutiny of their realism was urged, given the risk of relying on overly strong or untestable premises. The potential of metaheuristic algorithms was highlighted for efficiently identifying optimal designs across different model assumptions, supporting robustness evaluations. Practical implementation should adapt optimal designs to stakeholder needs while preserving acceptable statistical efficiency. In sum, advancing the adoption of innovative designs requires improved communication, infrastructure, and methodological transparency, alongside careful evaluation of model assumptions and robustness.

Clinical TrialsVol. 22(4)
University of Toronto (CA), University of Michigan (US), Hospital for Sick Children (CA), Public Health Ontario (CA), SickKids Foundation (CA), Institute for Clinical Evaluative Sciences (CA), University College London (GB)
Industry, innovation and infrastructure
Openalex Percentile: Top 85%
Statistical Methods in Clinical Trials
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