共 71 条
[1]
Zhou H(2018)Accuracy, safety, and reliability of novel phase I trial designs Clin Cancer Res. 24 4357-64
[2]
Yuan Y(1989)Design and analysis of phase I clinical trials Biometrics. 45 925-37
[3]
Nie L(1999)Operating characteristics of the standard phase I clinical trial design Comput Stat Data Anal. 30 303-15
[4]
Storer BE(2009)Dose escalation methods in phase I cancer clinical trials J Natl Cancer Inst. 101 708-20
[5]
Reiner E(1990)Continual reassessment method: a practical design for phase I clinical trials in cancer Biometrics. 46 33-48
[6]
Paoletti X(1998)Cancer Phase I Clinical Trials: efficient dose escalation with overdose control Stat Med. 17 1103-20
[7]
O’Quigley J(2010)Dose Finding with Escalation with Overdose Control (EWOC) in Cancer Clinical Trials Stat Sci. 25 217-26
[8]
Le Tourneau C(2008)Critical aspects of the Bayesian approach to phase I cancer trials Stat Med. 27 2420-39
[9]
Lee JJ(2010)A modified toxicity probability interval method for dose-finding trials Clin Trials. 7 653-63
[10]
Siu LL(2017)A Bayesian interval dose-finding design addressing Ockham’s razor: mTPI-2 Contemp Clin Trials. 58 23-33