Comparison Among Modified Continual Reassessment Methods with Different Dose Allocation Methods for Phase I Clinical Trials

The continual reassessment method (CRM) has been an essential Bayesian finding design in phase I clinical trials. It utilizes all the information in observed data which contributes to its essential operational characteristics. However, the CRM has been criticized for its aggressive dose escalation. Model-assisted methods including BOIN, Keyboard, and mTPI improved the safety while retaining relative efficiency. In this paper, we propose four models combining the structure of the CRM and model-assisted methods. We show that these models could operate with comparable CRM performance through simulations. The results suggest that two of the proposed methods outperformed the traditional methods with a higher percentage of correct selection of true maximum tolerated dose. In addition, the interval-based approaches offered by the new models with greater flexibility regarding target toxicity achieved an improvement in the adaptability of the dose-finding process in clinical trials.

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Publication Details

Journal
Mathematics
Published
2025-03-05
DOI
https://doi.org/10.3390/math13050863
Primary Topic
Statistical Methods in Clinical Trials
Type
article
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article

Comparison Among Modified Continual Reassessment Methods with Different Dose Allocation Methods for Phase I Clinical Trials

Conghua Wen, Rong Li, Weijia Zhang, Jiacheng Xiao
Mathematics
Statistical Methods in Clinical Trials
article

Comparison Among Modified Continual Reassessment Methods with Different Dose Allocation Methods for Phase I Clinical Trials

Conghua Wen, Rong Li, Weijia Zhang, Jiacheng Xiao
article en

Abstract

The continual reassessment method (CRM) has been an essential Bayesian finding design in phase I clinical trials. It utilizes all the information in observed data which contributes to its essential operational characteristics. However, the CRM has been criticized for its aggressive dose escalation. Model-assisted methods including BOIN, Keyboard, and mTPI improved the safety while retaining relative efficiency. In this paper, we propose four models combining the structure of the CRM and model-assisted methods. We show that these models could operate with comparable CRM performance through simulations. The results suggest that two of the proposed methods outperformed the traditional methods with a higher percentage of correct selection of true maximum tolerated dose. In addition, the interval-based approaches offered by the new models with greater flexibility regarding target toxicity achieved an improvement in the adaptability of the dose-finding process in clinical trials.

MathematicsVol. 13(5)
Xi’an Jiaotong-Liverpool University (CN)
Openalex Percentile: Top 96%
Statistical Methods in Clinical Trials
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