메뉴 건너뛰기




Volumn , Issue , 2006, Pages 225-242

Dose-Finding with Delayed Binary Outcomes in Cancer Trials

Author keywords

Chronic toxicity formulation; Correct weight function; Dose finding methods in delayed toxicity outcomes; Dose finding with delayed binary outcomes; IMRT scenarios; Intensity modulated radiation therapy (IMRT); Simulation; Time to event approach and likelihood based dose finding methods; TITE CRM

Indexed keywords

TOXICITY;

EID: 84957974628     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/0470861258.ch11     Document Type: Chapter
Times cited : (1)

References (20)
  • 1
    • 0023554115 scopus 로고
    • Current phase I/II designs: are they adequate?
    • B. Storer and D. DeMets (1987) Current phase I/II designs: are they adequate? J. Clin. Res. Drug Development, 1, 121-30.
    • (1987) J. Clin. Res. Drug Development , vol.1 , pp. 121-130
    • Storer, B.1    DeMets, D.2
  • 2
    • 0024452804 scopus 로고
    • Design and analysis of phase I clinical trial
    • B.E. Storer (1989) Design and analysis of phase I clinical trial. Biometrics, 45(3), 925-37.
    • (1989) Biometrics , vol.45 , Issue.3 , pp. 925-937
    • Storer, B.E.1
  • 3
    • 0025148278 scopus 로고
    • Continual reassessment method: a practical design for phase I clinical trials in cancer
    • J. O'Quigley, M. Pepe and L. Fisher (1990) Continual reassessment method: a practical design for phase I clinical trials in cancer. Biometrics, 46(1), 33-48.
    • (1990) Biometrics , vol.46 , Issue.1 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 4
    • 0031920799 scopus 로고    scopus 로고
    • Cancer phase I clinical trials: efficient dose escalation with overdose control
    • J. Babb, A. Rogatko and S. Zacks (1998) Cancer phase I clinical trials: efficient dose escalation with overdose control. Statistics in Medicine, 17(10), 1103-20.
    • (1998) Statistics in Medicine , vol.17 , Issue.10 , pp. 1103-1120
    • Babb, J.1    Rogatko, A.2    Zacks, S.3
  • 5
    • 84957940101 scopus 로고    scopus 로고
    • Dose escalation strategies for phase I clinical trials with late-onset toxicities
    • PhD Dissertation, University of Wisconsin, Madison, Wisconsin
    • Y.K. Cheung (2000) Dose escalation strategies for phase I clinical trials with late-onset toxicities. PhD Dissertation, University of Wisconsin, Madison, Wisconsin.
    • (2000)
    • Cheung, Y.K.1
  • 6
    • 0033637096 scopus 로고    scopus 로고
    • Sequential designs for phase I clinical trials with late-onset toxicities
    • Y.K. Cheung and R. Chappell (2000) Sequential designs for phase I clinical trials with late-onset toxicities. Biometrics, 56(4), 1177-82.
    • (2000) Biometrics , vol.56 , Issue.4 , pp. 1177-1182
    • Cheung, Y.K.1    Chappell, R.2
  • 8
    • 0029027770 scopus 로고
    • Some practical improvements in the continual reassessment method for phase I studies
    • S.N. Goodman, M.L. Zahurak and S. Piantadosi (1995) Some practical improvements in the continual reassessment method for phase I studies. Statistics in Medicine, 14(11), 1149-61.
    • (1995) Statistics in Medicine , vol.14 , Issue.11 , pp. 1149-1161
    • Goodman, S.N.1    Zahurak, M.L.2    Piantadosi, S.3
  • 9
    • 0033617666 scopus 로고    scopus 로고
    • Accrual strategies for phase I trials with delayed patient outcome
    • P.F. Thall, J.J. Lee, C.H. Tseng and E.H. Estey (1999) Accrual strategies for phase I trials with delayed patient outcome. Statistics in Medicine, 18(10), 1155-69.
    • (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
  • 11
    • 0036186030 scopus 로고    scopus 로고
    • Monitoring the rates of composite events with censored data in phase II clinical trials
    • Y.K. Cheung and P.F. Thall (2002) Monitoring the rates of composite events with censored data in phase II clinical trials. Biometrics, 58(1), 89-97.
    • (2002) Biometrics , vol.58 , Issue.1 , pp. 89-97
    • Cheung, Y.K.1    Thall, P.F.2
  • 12
    • 0031888716 scopus 로고    scopus 로고
    • Practical implementation of a modified continual reassessment method for dose-finding trials
    • S. Piantadosi, J.D. Fisher and S. Grossman (1998) Practical implementation of a modified continual reassessment method for dose-finding trials. Cancer Chemotherapy and Pharmacology, 41(6), 429-36.
    • (1998) Cancer Chemotherapy and Pharmacology , vol.41 , Issue.6 , pp. 429-436
    • Piantadosi, S.1    Fisher, J.D.2    Grossman, S.3
  • 13
    • 0000481188 scopus 로고
    • An empirical distribution function for sampling with incomplete information
    • M. Ayer, H.D. Brunk, G.M. Ewing, W.T. Reid and E. Silverman (1955) An empirical distribution function for sampling with incomplete information. Ann. Math. Statistics, 26, 641-7.
    • (1955) Ann. Math. Statistics , vol.26 , pp. 641-647
    • Ayer, M.1    Brunk, H.D.2    Ewing, G.M.3    Reid, W.T.4    Silverman, E.5
  • 14
  • 15
    • 0029129572 scopus 로고
    • Semi-parametric estimation in failure time mixture models
    • J.M. Taylor (1995) Semi-parametric estimation in failure time mixture models. Biometrics, 51(3), 899-907.
    • (1995) Biometrics , vol.51 , Issue.3 , pp. 899-907
    • Taylor, J.M.1
  • 16
    • 0000247147 scopus 로고
    • Estimation and testing in a two-sample generalized odds-rate model
    • D.M. Dabrowska and K.A. Doksum (1988) Estimation and testing in a two-sample generalized odds-rate model. J. Am. Statistical Assoc., 83, 744-9.
    • (1988) J. Am. Statistical Assoc. , vol.83 , pp. 744-749
    • Dabrowska, D.M.1    Doksum, K.A.2
  • 17
    • 0036712359 scopus 로고    scopus 로고
    • A simple technique to evaluate model sensitivity in the continual reassessment method
    • Y.K. Cheung and R. Chappell (2002) A simple technique to evaluate model sensitivity in the continual reassessment method. Biometrics, 58(3), 671-4.
    • (2002) Biometrics , vol.58 , Issue.3 , pp. 671-674
    • Cheung, Y.K.1    Chappell, R.2
  • 18
    • 0028060511 scopus 로고
    • Practical modifications of the continual reassessment method for phase I cancer clinical trials
    • D. Faries (1994) Practical modifications of the continual reassessment method for phase I cancer clinical trials. J. Biopharmaceutical Statistics, 4(2), 147-64.
    • (1994) J. Biopharmaceutical Statistics , vol.4 , Issue.2 , pp. 147-164
    • Faries, D.1
  • 19
    • 0031953966 scopus 로고    scopus 로고
    • A strategy for dose-finding and safety monitoring based on efficacy and adverse outcomes in phase I/II clinical trials
    • P.F. Thall and K.E. Russell (1998) A strategy for dose-finding and safety monitoring based on efficacy and adverse outcomes in phase I/II clinical trials. Biometrics, 54(1), 251-64.
    • (1998) Biometrics , vol.54 , Issue.1 , pp. 251-264
    • Thall, P.F.1    Russell, K.E.2
  • 20
    • 0034533856 scopus 로고    scopus 로고
    • Longitudinal design for phase I clinical trials using the continual reassessment method
    • A.T.R. Legedza and J.G. Ibrahim (2000) Longitudinal design for phase I clinical trials using the continual reassessment method. Controlled Clin. Trials, 21(6), 574-88.
    • (2000) Controlled Clin. Trials , vol.21 , Issue.6 , pp. 574-588
    • Legedza, A.T.R.1    Ibrahim, J.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.