참고문헌
- A'Hern RP (2001). Sample size tables for exact single-stage phase II designs, Statistics in Medicine, 20, 859-866. https://doi.org/10.1002/sim.721
- Bryant J and Day R (1995). Incorporating toxicity considerations into the design of two-stage phase ii clinical trials, Biometrics, 51, 1372-1383. https://doi.org/10.2307/2533268
- Cai C, Liu S, and Yuan Y (2014). A Bayesian design for phase II clinical trials with delayed responses based on multiple imputation, Statistics in Medicine, 33, 4017-4028. https://doi.org/10.1002/sim.6200
- Chen K and Shan M (2007). Optimal and minimax three-stage designs for phase II oncology clinical trials, Contemporary Clinical Trials, 28, 32-41.
- Chen TT (1997). Optimal three-stage designs for phase II cancer clinical trials, Statistics in Medicine, 16, 2701-2711. https://doi.org/10.1002/(SICI)1097-0258(19971215)16:23<2701::AID-SIM704>3.0.CO;2-1
- Conaway MR and Petroni GR (1996). Designs for phase ii trials allowing for a trade-off between response and toxicity, Biometrics, 52, 1375-1386. https://doi.org/10.2307/2532851
- Ensign LG, Gehan EA, Kamen DS, and Thall PF (1994). An optimal three-stage design for phase II clinical trials, Statistics in Medicine, 13, 1727-1736. https://doi.org/10.1002/sim.4780131704
- Fleming TR (1982). One-sample multiple testing procedure for phase ii clinical trials, Biometrics, 38, 143-151. https://doi.org/10.2307/2530297
- Green SJ and Dahlberg S (1992). Planned versus attained design in phase II clinical trials, Statistics in Medicine, 11, 853-862. https://doi.org/10.1002/sim.4780110703
- Jung SH, Carey M, and Kim KM (2001). Graphical search for two-stage designs for phase II clinical trials, Controlled Clinical Trials, 22, 367-372. https://doi.org/10.1016/S0197-2456(01)00142-8
- Kim S and Wong WK (2017). Extended two-stage adaptive designs with three target responses for phase II clinical trials, Statistical Methods in Medical Research, 27, 3628-3642.
- Kwak M and Jung SH (2014). Phase II clinical trials with time-to-event endpoints: optimal two-stage designs with one-sample log-rank test, Statistics in Medicine, 33, 2004-2016. https://doi.org/10.1002/sim.6073
- Lee JJ and Liu DD (2008). A predictive probability design for phase II cancer clinical trials, Clinical Trials, 5, 93-106. https://doi.org/10.1177/1740774508089279
- Mander AP and Thompson SG (2010). Two-stage designs optimal under the alternative hypothesis for phase II cancer clinical trials, Contemporary Clinical Trials, 31, 572-578. https://doi.org/10.1016/j.cct.2010.07.008
- Mander AP, Wason JM, Sweeting MJ, and Thompson SG (2012). Admissible two-stage designs for phase II cancer clinical trials that incorporate the expected sample size under the alternative hypothesis, Pharmaceutical Statistics, 11, 91-96. https://doi.org/10.1002/pst.501
- Ray HE and Rai SN (2011). An evaluation of a Simon 2-stage phase II clinical trial design incorporating toxicity monitoring, Contemporary Clinical Trials, 32, 428-436. https://doi.org/10.1016/j.cct.2011.01.006
- Rugo HS, Seneviratne L, Beck JT, et al. (2017). Prevention of everolimus-related stomatitis in women with hormone receptor-positive, her2-negative metastatic breast cancer using dexamethasone mouthwash (SWISH): a single-arm, phase 2 trial, Lancet Oncol, 18, 654-662. https://doi.org/10.1016/S1470-2045(17)30109-2
- Simon R (1989). Optimal two-stage designs for phase II clinical trials, Controlled Clinical Trials, 10, 1-10. https://doi.org/10.1016/0197-2456(89)90015-9
- Thall PF and Simon R (1994). Practical Bayesian guidelines for phase IIB clinical trials, Biometrics, 50, 337-349. https://doi.org/10.2307/2533377
- Wason JM, Mander AP, and Eisen TG (2011). Reducing sample sizes in two-stage phase II cancer trials by using continuous tumour shrinkage end-points, European Journal of Cancer, 47, 983-989. https://doi.org/10.1016/j.ejca.2010.12.007
- Zhou H, Lee JJ, and Yuan Y (2017). BOP2: Bayesian optimal design for phase II clinical trials with simple and complex endpoints, Statistics in Medicine, 36, 3302-3314. https://doi.org/10.1002/sim.7338