메뉴 건너뛰기




Volumn 30, Issue 17, 2011, Pages 2057-2061

Continual reassessment and related designs in dose-finding studies

Author keywords

[No Author keywords available]

Indexed keywords

BAYES THEOREM; CONFLICT OF INTEREST; CONTINUAL REASSESSMENT METHOD; DOSE CALCULATION; EDITORIAL; FACTORIAL DESIGN; HARM REDUCTION; HUMAN; MATHEMATICAL MODEL; MAXIMUM LIKELIHOOD METHOD; MAXIMUM TOLERATED DOSE; PATIENT SELECTION; RANDOMIZATION; RISK ASSESSMENT; SAMPLE SIZE; SENSITIVITY ANALYSIS; STUDY DESIGN;

EID: 79959997003     PISSN: 02776715     EISSN: 10970258     Source Type: Journal    
DOI: 10.1002/sim.4215     Document Type: Editorial
Times cited : (12)

References (20)
  • 2
    • 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(14):1537-1549.
    • (1998) Statistics in Medicine , vol.17 , Issue.14 , pp. 1537-1549
    • Ahn, C.1
  • 3
    • 0029780751 scopus 로고    scopus 로고
    • Improved designs for dose escalation studies using pharmacokinetic measurements
    • Piantadosi S, Liu G. Improved designs for dose escalation studies using pharmacokinetic measurements. Statistics in Medicine 1996; 15(15):1605-1618.
    • (1996) Statistics in Medicine , vol.15 , Issue.15 , pp. 1605-1618
    • Piantadosi, S.1    Liu, G.2
  • 4
    • 0031670630 scopus 로고    scopus 로고
    • Bayesian decision procedures based on logistic regression models for dose-finding studies
    • Whitehead J, Williamson D. Bayesian decision procedures based on logistic regression models for dose-finding studies. Journal of Biopharmaceutical Statistics 1998; 8:445-467.
    • (1998) Journal of Biopharmaceutical Statistics , vol.8 , pp. 445-467
    • Whitehead, J.1    Williamson, D.2
  • 5
    • 0033617666 scopus 로고    scopus 로고
    • Accrual strategies for phase I trials with delayed patient outcome
    • Thall PF, Lee JJ, Tseng CH, Estey EH. Accrual strategies for phase I trials with delayed patient outcome. Statistics in Medicine 1999; 18(10):1155-1169.
    • (1999) Statistics in Medicine , vol.18 , Issue.10 , pp. 1155-1169
    • Thall, P.F.1    Lee, J.J.2    Tseng, C.H.3    Estey, E.H.4
  • 6
    • 0035974939 scopus 로고    scopus 로고
    • An evaluation of phase I clinical trial designs in the continuous dose-response setting
    • Storer B. An evaluation of phase I clinical trial designs in the continuous dose-response setting. Statistics in Medicine 2001; 20(16):2399-2408.
    • (2001) Statistics in Medicine , vol.20 , Issue.16 , pp. 2399-2408
    • Storer, B.1
  • 7
    • 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(1):33-48.
    • (1990) Biometrics , vol.46 , Issue.1 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 8
    • 0029027770 scopus 로고
    • Some practical improvements in the continual reassessment method for phase I studies
    • Goodman SN, Zahurak ML, Piantadosi S. Some practical improvements in the continual reassessment method for phase I studies. Statistics in Medicine 1995; 14(11):1149-1161.
    • (1995) Statistics in Medicine , vol.14 , Issue.11 , pp. 1149-1161
    • Goodman, S.N.1    Zahurak, M.L.2    Piantadosi, S.3
  • 9
    • 59349088647 scopus 로고    scopus 로고
    • A comprehensive comparison of the continual reassessment method 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 method 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
  • 10
    • 0033619523 scopus 로고    scopus 로고
    • Another look at two phase I clinical trial designs (with commentary)
    • O'Quigley J. Another look at two phase I clinical trial designs (with commentary). Statistics in Medicine 1999; 18:2683-2692.
    • (1999) Statistics in Medicine , vol.18 , pp. 2683-2692
    • O'Quigley, J.1
  • 12
    • 0031920799 scopus 로고    scopus 로고
    • Cancer phase I clinical trials: efficient dose escalation with overdose control
    • Babb J, Rogatko A, Zacks S. Cancer phase I clinical trials: efficient dose escalation with overdose control. Statistics in Medicine 1998; 17(10):1103-1120.
    • (1998) Statistics in Medicine , vol.17 , Issue.10 , pp. 1103-1120
    • Babb, J.1    Rogatko, A.2    Zacks, S.3
  • 13
    • 79959983813 scopus 로고    scopus 로고
    • Two-stage continual reassessment method that determines dose-escalation based on individual toxicity grades. Society of Clinical Trials 31st Annual Meeting, 2010 (abstract P94).
    • Iasonos A, Zohar S, O'Quigley J. Two-stage continual reassessment method that determines dose-escalation based on individual toxicity grades. Society of Clinical Trials 31st Annual Meeting, 2010 (abstract P94).
    • Iasonos, A.1    Zohar, S.2    O'Quigley, J.3
  • 14
  • 15
    • 27944494441 scopus 로고    scopus 로고
    • Coherence principles in dose-finding studies
    • Cheung YK. Coherence principles in dose-finding studies. Biometrika 2005; 92(4):863-873.
    • (2005) Biometrika , vol.92 , Issue.4 , pp. 863-873
    • Cheung, Y.K.1
  • 16
    • 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(1):57-71.
    • (2006) Clinical Trials , vol.3 , Issue.1 , pp. 57-71
    • Garrett-Mayer, E.1
  • 17
    • 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
  • 18
    • 70349776681 scopus 로고    scopus 로고
    • Bayesian model averaging continual reassessment method in phase I clinical trials
    • Yin G, Yuan Y. Bayesian model averaging continual reassessment method in phase I clinical trials. Journal of the American Statistical Association 2009; 104(487):954-968.
    • (2009) Journal of the American Statistical Association , vol.104 , Issue.487 , pp. 954-968
    • Yin, G.1    Yuan, Y.2
  • 19
    • 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
  • 20
    • 77952967060 scopus 로고    scopus 로고
    • Utility-based optimization of combination therapy using ordinal toxicity and efficacy in phase I/II trials
    • Houede N, Thall PF, Nguyen H, Paoletti X, Kramar A. Utility-based optimization of combination therapy using ordinal toxicity and efficacy in phase I/II trials. Biometrics 2010; 66(2):532-540.
    • (2010) Biometrics , vol.66 , Issue.2 , pp. 532-540
    • Houede, N.1    Thall, P.F.2    Nguyen, H.3    Paoletti, X.4    Kramar, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.