OncoBayes2 (Q52525): Difference between revisions

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+Bayesian logistic regression model with optional  EXchangeability-NonEXchangeability parameter modelling for flexible  borrowing from historical or concurrent data-sources. The safety model  can guide dose-escalation decisions for adaptive oncology Phase I  dose-escalation trials which involve an arbitrary number of  drugs. Please refer to Neuenschwander et al. (2008)  <doi:10.1002/sim.3230> and Neuenschwander et al. (2016)  <doi:10.1080/19466315.2016.1174149> for details on the methodology.
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Latest revision as of 02:33, 22 March 2024

Bayesian Logistic Regression for Oncology Dose-Escalation Trials

Language	Label	Description	Also known as
English	OncoBayes2	Bayesian Logistic Regression for Oncology Dose-Escalation Trials

Statements

instance of

R package

0 references

software version identifier

0.8-8

publication date

3 March 2023

0 references

0.4-4

publication date

29 August 2019

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0.5-3

publication date

15 November 2019

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0.5-4

publication date

19 November 2019

0 references

0.5-8

publication date

12 December 2019

0 references

0.6-0

publication date

11 February 2020

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0.6-3

publication date

19 March 2020

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0.6-4

publication date

7 April 2020

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0.6-5

publication date

7 May 2020

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0.7-0

publication date

7 May 2021

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0.8-1

publication date

2 September 2021

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0.8-2

publication date

14 September 2021

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0.8-4

publication date

18 February 2022

0 references

0.8-5

publication date

1 March 2022

0 references

0.8-6

publication date

2 May 2022

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0.8-7

publication date

25 August 2022

0 references

0.8-9

publication date

20 July 2023

0 references

0 references

0 references

MaRDI software profile

0 references

last update

20 July 2023

0 references

description

Bayesian logistic regression model with optional EXchangeability-NonEXchangeability parameter modelling for flexible borrowing from historical or concurrent data-sources. The safety model can guide dose-escalation decisions for adaptive oncology Phase I dose-escalation trials which involve an arbitrary number of drugs. Please refer to Neuenschwander et al. (2008) <doi:10.1002/sim.3230> and Neuenschwander et al. (2016) <doi:10.1080/19466315.2016.1174149> for details on the methodology.

0 references

0 references

0 references

0 references

GNU General Public License

edition/version

≥ 3 (English)