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Volumn 30, Issue 17, 2011, Pages 2117-2129

Estimating the dose-toxicity curve in completed phase I studies

Author keywords

Constrained maximum likelihood estimation; Dose toxicity curve; Phase I trial; Retrospective continual reassessment method; Small sample size

Indexed keywords

ACCURACY; ARTICLE; CONFIDENCE INTERVAL; CONTROLLED STUDY; DOSE CALCULATION; INTERMETHOD COMPARISON; MAXIMUM LIKELIHOOD METHOD; MAXIMUM TOLERATED DOSE; NONPARAMETRIC TEST; PLOTS AND CURVES; PROBABILITY; REGRESSION ANALYSIS; SEQUENTIAL ANALYSIS; STUDY DESIGN;

EID: 79959925159     PISSN: 02776715     EISSN: 10970258     Source Type: Journal    
DOI: 10.1002/sim.4206     Document Type: Article
Times cited : (12)

References (29)
  • 3
    • 0032581450 scopus 로고    scopus 로고
    • An evaluation of Phase I cancer clinical trial designs
    • Ahn C. An evaluation of Phase I cancer clinical trial designs. Statistics in Medicine 1998; 17:1537-1549.
    • (1998) Statistics in Medicine , vol.17 , pp. 1537-1549
    • Ahn, C.1
  • 4
    • 33644597596 scopus 로고    scopus 로고
    • The continual reassessment method for dose-finding studies: A tutorial
    • Garrett Mayer E. The continual reassessment method for dose-finding studies: A tutorial. Clinical Trials 2006; 3:57-71.
    • (2006) Clinical Trials , vol.3 , pp. 57-71
    • Garrett Mayer, E.1
  • 5
    • 33745453653 scopus 로고    scopus 로고
    • A model-based approach in the estimation of the maximum tolerated dose in phase I cancer clinical trials
    • He W, Liu J, Binkowitz B, Quan H. A model-based approach in the estimation of the maximum tolerated dose in phase I cancer clinical trials. Statistics in Medicine 2006; 25:2027-2042.
    • (2006) Statistics in Medicine , vol.25 , pp. 2027-2042
    • He, W.1    Liu, J.2    Binkowitz, B.3    Quan, H.4
  • 6
    • 59349088647 scopus 로고    scopus 로고
    • A comprehensive comparison of the continual reassessment mehod to the standard 3 + 3 dose escalation scheme in Phase I dose-finding studies
    • Iasonos A, Wilton AS, Riedel ER, Seshan VE, Spriggs DR. A comprehensive comparison of the continual reassessment mehod to the standard 3 + 3 dose escalation scheme in Phase I dose-finding studies. Clinical Trials 2008; 5:465-477.
    • (2008) Clinical Trials , vol.5 , pp. 465-477
    • Iasonos, A.1    Wilton, A.S.2    Riedel, E.R.3    Seshan, V.E.4    Spriggs, D.R.5
  • 7
    • 59349096738 scopus 로고    scopus 로고
    • Quality assessment of phase I dose-finding cancer trials: Proposal of a checklist
    • Zohar S, Lian Q, Levy V, Cheung K, Ivanova A, Chevret S. Quality assessment of phase I dose-finding cancer trials: Proposal of a checklist. Clinical Trials 2008; 5:478-485.
    • (2008) Clinical Trials , vol.5 , pp. 478-485
    • Zohar, S.1    Lian, Q.2    Levy, V.3    Cheung, K.4    Ivanova, A.5    Chevret, S.6
  • 8
    • 0025148278 scopus 로고
    • Continual reassessment method: A practical design for phase 1 clinical trials in cancer
    • O'Quigley J, Pepe M, Fisher L. Continual reassessment method: A practical design for phase 1 clinical trials in cancer. Biometrics 1990; 46:33-48.
    • (1990) Biometrics , vol.46 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 9
    • 0017054227 scopus 로고
    • A generalization of the probit and logit methods for dose response curves
    • Prentice RL. A generalization of the probit and logit methods for dose response curves. Biometrics 1976; 32:761-768.
    • (1976) Biometrics , vol.32 , pp. 761-768
    • Prentice, R.L.1
  • 10
    • 0001400118 scopus 로고
    • Sigmoidally constrained maximum likelihood estimation in quantal bioassay
    • Schmoyer RL. Sigmoidally constrained maximum likelihood estimation in quantal bioassay. Journal of the American Statistical Association 1984; 79:448-453.
    • (1984) Journal of the American Statistical Association , vol.79 , pp. 448-453
    • Schmoyer, R.L.1
  • 13
    • 0034651978 scopus 로고    scopus 로고
    • A semiparametric approach to analysing dose-response data
    • Nottingham QJ, Birch JB. A semiparametric approach to analysing dose-response data. Statistics in Medicine 2000; 19:389-404.
    • (2000) Statistics in Medicine , vol.19 , pp. 389-404
    • Nottingham, Q.J.1    Birch, J.B.2
  • 14
    • 0024204438 scopus 로고
    • Kernel estimates of dose response
    • Staniswalis JG, Cooper V. Kernel estimates of dose response. Biometrics 1988; 44:1103-1119.
    • (1988) Biometrics , vol.44 , pp. 1103-1119
    • Staniswalis, J.G.1    Cooper, V.2
  • 15
    • 0036191646 scopus 로고    scopus 로고
    • Dose finding using the biased coin up-and-down design and isotonic regression
    • Stylianou M, Flournoy N. Dose finding using the biased coin up-and-down design and isotonic regression. Biometrics 2002; 58:171-177.
    • (2002) Biometrics , vol.58 , pp. 171-177
    • Stylianou, M.1    Flournoy, N.2
  • 16
    • 0037470293 scopus 로고    scopus 로고
    • Estimating the probability of toxicity at the target dose following an up-and-down design
    • Stylianou M, Proschan M, Flournoy N. Estimating the probability of toxicity at the target dose following an up-and-down design. Statistics in Medicine 2003; 22:535-543.
    • (2003) Statistics in Medicine , vol.22 , pp. 535-543
    • Stylianou, M.1    Proschan, M.2    Flournoy, N.3
  • 17
    • 27744594554 scopus 로고    scopus 로고
    • Retrospective analysis of sequential dose-finding designs
    • O'Quigley J. Retrospective analysis of sequential dose-finding designs. Biometrics 2005; 61:749-756.
    • (2005) Biometrics , vol.61 , pp. 749-756
    • O'Quigley, J.1
  • 18
    • 0029938415 scopus 로고    scopus 로고
    • Continual reassessment method: a likelihood approach
    • O'Quigley J, Shen L. Continual reassessment method: a likelihood approach. Biometrics 1996; 52:673-684.
    • (1996) Biometrics , vol.52 , pp. 673-684
    • O'Quigley, J.1    Shen, L.2
  • 19
    • 33644840022 scopus 로고    scopus 로고
    • Experimental designs for phase I and phase I/II dose-finding studies
    • O'Quigley J, Zohar S. Experimental designs for phase I and phase I/II dose-finding studies. British Journal of Cancer 2006; 94:609-613.
    • (2006) British Journal of Cancer , vol.94 , pp. 609-613
    • O'Quigley, J.1    Zohar, S.2
  • 21
    • 18844419240 scopus 로고    scopus 로고
    • A Bayesian evaluation of enrolling additional patients at the maximum tolerated dose in phase I trials
    • Gonen M. A Bayesian evaluation of enrolling additional patients at the maximum tolerated dose in phase I trials. Controlled Clinical Trials 2005; 26:131-140.
    • (2005) Controlled Clinical Trials , vol.26 , pp. 131-140
    • Gonen, M.1
  • 27
    • 0032377357 scopus 로고    scopus 로고
    • Approximate is better than exact for interval estimation of binomial proportions
    • 8.
    • Agresti A, Coull B. Approximate is better than exact for interval estimation of binomial proportions. The American Statistician 1998; 52:8.
    • (1998) The American Statistician , vol.52
    • Agresti, A.1    Coull, B.2
  • 28
    • 0024237386 scopus 로고
    • Small-sample confidence limits for parameters under inequality constraints with application to quantal bioassay
    • Morris MD. Small-sample confidence limits for parameters under inequality constraints with application to quantal bioassay. Biometrics 1988; 44:1083-1092.
    • (1988) Biometrics , vol.44 , pp. 1083-1092
    • Morris, M.D.1
  • 29
    • 1142304984 scopus 로고    scopus 로고
    • Non-parametric optimal design in dose finding studies
    • O'Quigley J, Paoletti XJM. Non-parametric optimal design in dose finding studies. Biostatistics 2002; 3:51-56.
    • (2002) Biostatistics , vol.3 , pp. 51-56
    • O'Quigley, J.1    Paoletti, X.J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.