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1
Continual reassessment and related designs in dose-finding studies.
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A comparison of phase I dose-finding designs in clinical trials with monotonicity assumption violation.
Clin Trials. 2020 Oct;17(5):522-534. doi: 10.1177/1740774520932130. Epub 2020 Jul 7.
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Shift models for dose-finding in partially ordered groups.
Clin Trials. 2019 Feb;16(1):32-40. doi: 10.1177/1740774518801599. Epub 2018 Oct 11.
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The continual reassessment method for dose-finding studies: a tutorial.
Clin Trials. 2006;3(1):57-71. doi: 10.1191/1740774506cn134oa.
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Extended model-based designs for more complex dose-finding studies.
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6
Retrospective analysis of sequential dose-finding designs.
Biometrics. 2005 Sep;61(3):749-56. doi: 10.1111/j.1541-0420.2005.00353.x.
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Evaluation of irrational dose assignment definitions using the continual reassessment method.
Clin Trials. 2019 Dec;16(6):665-672. doi: 10.1177/1740774519873316. Epub 2019 Sep 23.
8
How to design a dose-finding study using the continual reassessment method.
BMC Med Res Methodol. 2019 Jan 18;19(1):18. doi: 10.1186/s12874-018-0638-z.
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Comparative review of novel model-assisted designs for phase I clinical trials.
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Incorporating lower grade toxicity information into dose finding designs.
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A nonparametric Bayesian method for dose finding in drug combinations cancer trials.
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Bayesian Optimal Interval Design: A Simple and Well-Performing Design for Phase I Oncology Trials.
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Adaptive dose-finding studies: a review of model-guided phase I clinical trials.
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BAYESIAN DATA AUGMENTATION DOSE FINDING WITH CONTINUAL REASSESSMENT METHOD AND DELAYED TOXICITY.
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Adaptive prior variance calibration in the Bayesian continual reassessment method.
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本文引用的文献

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Utility-based optimization of combination therapy using ordinal toxicity and efficacy in phase I/II trials.
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Translation of innovative designs into phase I trials.
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The continual reassessment method for dose-finding studies: a tutorial.
Clin Trials. 2006;3(1):57-71. doi: 10.1191/1740774506cn134oa.
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Experimental designs for phase I and phase I/II dose-finding studies.
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Retrospective analysis of sequential dose-finding designs.
Biometrics. 2005 Sep;61(3):749-56. doi: 10.1111/j.1541-0420.2005.00353.x.
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An evaluation of phase I clinical trial designs in the continuous dose-response setting.
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Another look at two phase I clinical trial designs.
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Accrual strategies for phase I trials with delayed patient outcome.
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Bayesian decision procedures based on logistic regression models for dose-finding studies.
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