A dose-schedule finding design for phase I-II clinical trials-Reference-Cited by-同舟云学术

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A dose-schedule finding design for phase I-II clinical trials

Published:2015-08-10 Issue:2 Volume:65 Page:259-272
ISSN:0035-9254
Container-title:Journal of the Royal Statistical Society: Series C (Applied Statistics)
language:en
Short-container-title:J. R. Stat. Soc. C

Author:

Guo Beibei¹,Li Yisheng²,Yuan Ying²

Affiliation:

1. Louisiana State University; Baton Rouge USA

2. University of Texas MD Anderson Cancer Center; Houston USA

Funder

National Cancer Institute

‘Stand up to cancer dream team translational research’

Entertainment Industry Foundation

Publisher

Wiley

Subject

Statistics, Probability and Uncertainty,Statistics and Probability

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/rssc.12113/fullpdf

Reference20 articles.

1. Bayesian analysis of binary and polytomous response data;Albert;J. Am. Statist. Ass.,1993

2. Influence of treatment schedule on toxicity and efficacy of cyclophosphamide, epirubicin, and fluorouracil in metastatic breast cancer: a randomized trial comparing weekly and every-4-week administration;Blomqvist;J. Clin. Oncol.,1993

3. Simultaneously optimizing dose and schedule of a new cytotoxic agent;Braun;Clin. Trials,2007

4. Determining a maximum-tolerated schedule of a cytotoxic agent;Braun;Biometrics,2005

5. A Bayesian dose finding design for oncology clinical trials of combinational biological agents;Cai;Appl. Statist.,2014

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3. Optimizing dose-schedule regimens with bayesian adaptive designs: opportunities and challenges;Frontiers in Pharmacology;2023-11-23

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