Accounting for uncertainty in the historical response rate of the standard treatment in single‐arm two‐stage designs based on Bayesian power functions
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[1] Chap T. Le. Applied categorical data analysis and translational research , 2010 .
[2] J. Bryant,et al. Incorporating toxicity considerations into the design of two-stage phase II clinical trials. , 1995, Biometrics.
[3] Sin-Ho Jung,et al. Randomized phase II trials with a prospective control , 2008, Statistics in medicine.
[4] D. Spiegelhalter,et al. Bayesian Approaches to Clinical Trials and Health-Care Evaluation: Spiegelhalter/Clinical Trials and Health-Care Evaluation , 2004 .
[5] Meinhard Kieser,et al. Sample size planning for phase II trials based on success probabilities for phase III , 2015, Pharmaceutical statistics.
[6] Stefania Gubbiotti. Classical and Bayesian power functions; their use in clinical trials. , 2008 .
[7] Valeria Sambucini. A Bayesian predictive strategy for an adaptive two-stage design in phase II clinical trials. , 2010, Statistics in medicine.
[8] R. Simon,et al. Optimal two-stage designs for phase II clinical trials. , 1989, Controlled clinical trials.
[9] Valeria Sambucini,et al. A Bayesian predictive two‐stage design for phase II clinical trials , 2008, Statistics in medicine.
[10] Fang Chen,et al. Use of historical control data for assessing treatment effects in clinical trials , 2014, Pharmaceutical statistics.
[11] W. Shih,et al. A Bayesian–frequentist two‐stage single‐arm phase II clinical trial design , 2012, Statistics in medicine.
[12] Ming Li,et al. Bayesian designs with frequentist and Bayesian error rate considerations , 2005, Statistical methods in medical research.
[13] Anastasios A Tsiatis,et al. Adaptive two‐stage designs in phase II clinical trials , 2006, Statistics in medicine.
[14] 敏雄 下川. Randomized Phase II Cancer Clinical Trials , 2015 .
[15] Matteo Cellamare,et al. A randomized two‐stage design for phase II clinical trials based on a Bayesian predictive approach , 2015, Statistics in medicine.
[16] Pierpaolo Brutti,et al. Robust Bayesian sample size determination in clinical trials , 2008, Statistics in medicine.
[17] T. Chen,et al. Optimal three-stage designs for phase II cancer clinical trials. , 1997, Statistics in medicine.
[18] Sujit K. Sahu,et al. A Bayesian method of sample size determination with practical applications , 2006 .
[19] Weichung J Shih,et al. Adaptive Two‐Stage Designs for Single‐Arm Phase IIA Cancer Clinical Trials , 2004, Biometrics.
[20] David Machin,et al. Bayesian two-stage designs for phase II clinical trials. , 2002, Statistics in medicine.
[21] Fei Wang,et al. A simulation-based approach to Bayesian sample size determination for performance under a given model and for separating models , 2002 .
[22] Daniel J Sargent,et al. Optimising the design of phase II oncology trials: the importance of randomisation. , 2009, European journal of cancer.
[23] Ying Yuan,et al. A Bayesian design for phase II clinical trials with delayed responses based on multiple imputation , 2014, Statistics in medicine.
[24] Morris L. Eaton,et al. On the Limiting Behavior of the “Probability of Claiming Superiority” in a Bayesian Context , 2013 .
[25] Fulvio De Santis. Sample Size Determination for Robust Bayesian Analysis , 2006 .
[26] Guosheng Yin,et al. Clinical Trial Design: Bayesian and Frequentist Adaptive Methods , 2011 .
[27] Hua Jin,et al. A design of phase II cancer trials using total and complete response endpoints , 2005, Statistics in medicine.
[28] C. Baey,et al. Effect of a misspecification of response rates on type I and type II errors, in a phase II Simon design. , 2011, European journal of cancer.
[29] D. Sargent,et al. Randomized phase II trials: inevitable or inadvisable? , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[30] M R Conaway,et al. Bivariate sequential designs for phase II trials. , 1995, Biometrics.
[31] Manish R. Sharma,et al. Randomized phase II trials: a long-term investment with promising returns. , 2011, Journal of the National Cancer Institute.
[32] A. Zelenetz,et al. Gemcitabine, vinorelbine, and pegylated liposomal doxorubicin (GVD), a salvage regimen in relapsed Hodgkin's lymphoma: CALGB 59804. , 2007, Annals of oncology : official journal of the European Society for Medical Oncology.
[33] P F Thall,et al. Practical Bayesian guidelines for phase IIB clinical trials. , 1994, Biometrics.