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Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic

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Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic. / Ewings, S.; Saunders, G.; Jaki, T. et al.
In: BMC Medical Research Methodology, Vol. 22, No. 1, 25, 20.01.2022.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Ewings, S, Saunders, G, Jaki, T & Mozgunov, P 2022, 'Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic', BMC Medical Research Methodology, vol. 22, no. 1, 25. https://doi.org/10.1186/s12874-022-01512-0

APA

Ewings, S., Saunders, G., Jaki, T., & Mozgunov, P. (2022). Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic. BMC Medical Research Methodology, 22(1), Article 25. https://doi.org/10.1186/s12874-022-01512-0

Vancouver

Ewings S, Saunders G, Jaki T, Mozgunov P. Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic. BMC Medical Research Methodology. 2022 Jan 20;22(1):25. doi: 10.1186/s12874-022-01512-0

Author

Ewings, S. ; Saunders, G. ; Jaki, T. et al. / Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic. In: BMC Medical Research Methodology. 2022 ; Vol. 22, No. 1.

Bibtex

@article{3574c357c8b24aa5ba2d0ff03e153384,
title = "Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic",
abstract = "Background: Modern designs for dose-finding studies (e.g., model-based designs such as continual reassessment method) have been shown to substantially improve the ability to determine a suitable dose for efficacy testing when compared to traditional designs such as the 3 + 3 design. However, implementing such designs requires time and specialist knowledge. Methods: We present a practical approach to developing a model-based design to help support uptake of these methods; in particular, we lay out how to derive the necessary parameters and who should input, and when, to these decisions. Designing a model-based, dose-finding trial is demonstrated using a treatment within the AGILE platform trial, a phase I/II adaptive design for novel COVID-19 treatments. Results: We present discussion of the practical delivery of AGILE, covering what information was found to support principled decision making by the Safety Review Committee, and what could be contained within a statistical analysis plan. We also discuss additional challenges we encountered in the study and discuss more generally what (unplanned) adaptations may be acceptable (or not) in studies using model-based designs. Conclusions: This example demonstrates both how to design and deliver an adaptive dose-finding trial in order to support uptake of these methods. ",
keywords = "Adaptive design, Bayesian, Dose escalation, Phase I",
author = "S. Ewings and G. Saunders and T. Jaki and P. Mozgunov",
year = "2022",
month = jan,
day = "20",
doi = "10.1186/s12874-022-01512-0",
language = "English",
volume = "22",
journal = "BMC Medical Research Methodology",
issn = "1471-2288",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Practical recommendations for implementing a Bayesian adaptive phase I design during a pandemic

AU - Ewings, S.

AU - Saunders, G.

AU - Jaki, T.

AU - Mozgunov, P.

PY - 2022/1/20

Y1 - 2022/1/20

N2 - Background: Modern designs for dose-finding studies (e.g., model-based designs such as continual reassessment method) have been shown to substantially improve the ability to determine a suitable dose for efficacy testing when compared to traditional designs such as the 3 + 3 design. However, implementing such designs requires time and specialist knowledge. Methods: We present a practical approach to developing a model-based design to help support uptake of these methods; in particular, we lay out how to derive the necessary parameters and who should input, and when, to these decisions. Designing a model-based, dose-finding trial is demonstrated using a treatment within the AGILE platform trial, a phase I/II adaptive design for novel COVID-19 treatments. Results: We present discussion of the practical delivery of AGILE, covering what information was found to support principled decision making by the Safety Review Committee, and what could be contained within a statistical analysis plan. We also discuss additional challenges we encountered in the study and discuss more generally what (unplanned) adaptations may be acceptable (or not) in studies using model-based designs. Conclusions: This example demonstrates both how to design and deliver an adaptive dose-finding trial in order to support uptake of these methods.

AB - Background: Modern designs for dose-finding studies (e.g., model-based designs such as continual reassessment method) have been shown to substantially improve the ability to determine a suitable dose for efficacy testing when compared to traditional designs such as the 3 + 3 design. However, implementing such designs requires time and specialist knowledge. Methods: We present a practical approach to developing a model-based design to help support uptake of these methods; in particular, we lay out how to derive the necessary parameters and who should input, and when, to these decisions. Designing a model-based, dose-finding trial is demonstrated using a treatment within the AGILE platform trial, a phase I/II adaptive design for novel COVID-19 treatments. Results: We present discussion of the practical delivery of AGILE, covering what information was found to support principled decision making by the Safety Review Committee, and what could be contained within a statistical analysis plan. We also discuss additional challenges we encountered in the study and discuss more generally what (unplanned) adaptations may be acceptable (or not) in studies using model-based designs. Conclusions: This example demonstrates both how to design and deliver an adaptive dose-finding trial in order to support uptake of these methods.

KW - Adaptive design

KW - Bayesian

KW - Dose escalation

KW - Phase I

U2 - 10.1186/s12874-022-01512-0

DO - 10.1186/s12874-022-01512-0

M3 - Journal article

VL - 22

JO - BMC Medical Research Methodology

JF - BMC Medical Research Methodology

SN - 1471-2288

IS - 1

M1 - 25

ER -