메뉴 건너뛰기




Volumn 58, Issue 5, 2009, Pages 719-736

Bayesian dose finding by jointly modelling toxicity and efficacy as time-to-event outcomes

Author keywords

Adaptive design; Bivariate survival function; Cure rate model; Phase I trial; Phase II trial; Survival curve

Indexed keywords


EID: 70350136475     PISSN: 00359254     EISSN: 14679876     Source Type: Journal    
DOI: 10.1111/j.1467-9876.2009.00674.x     Document Type: Article
Times cited : (95)

References (23)
  • 1
    • 0001086867 scopus 로고
    • Survival curve for cancer patients following treatment
    • Berkson, J. Gage, R. P. (1952) Survival curve for cancer patients following treatment. J. Am. Statist. Ass., 47, 501 515.
    • (1952) J. Am. Statist. Ass. , vol.47 , pp. 501-515
    • Berkson, J.1    Gage, R.P.2
  • 2
    • 33644861229 scopus 로고    scopus 로고
    • Bayesian clinical trials
    • Berry, D. A. (2006) Bayesian clinical trials. Nat. Rev. Drug Discov., 5, 27 36.
    • (2006) Nat. Rev. Drug Discov. , vol.5 , pp. 27-36
    • Berry, D.A.1
  • 3
    • 0036277621 scopus 로고    scopus 로고
    • The bivariate continual reassessment method: Extending the CRM to phase i trials of two competing outcomes
    • Braun, T. M. (2002) The bivariate continual reassessment method: extending the CRM to phase I trials of two competing outcomes. Contr. Clin. Trials, 23, 240 256.
    • (2002) Contr. Clin. Trials , vol.23 , pp. 240-256
    • Braun, T.M.1
  • 4
    • 34249289754 scopus 로고    scopus 로고
    • Simultaneously optimizing dose and schedule of a new cytotoxic agent
    • Braun, T. M., Thall, P. F., Nguyen, H. Lima, M. (2007) Simultaneously optimizing dose and schedule of a new cytotoxic agent. Clin. Trials, 4, 113 124.
    • (2007) Clin. Trials , vol.4 , pp. 113-124
    • Braun, T.M.1    Thall, P.F.2    Nguyen, H.3    Lima, M.4
  • 5
    • 20744450408 scopus 로고    scopus 로고
    • Determining a maximum tolerated schedule of a cytotoxic agent
    • Braun, T. M., Yuan, Z. Thall, P. F. (2005) Determining a maximum tolerated schedule of a cytotoxic agent. Biometrics, 61, 335 343.
    • (2005) Biometrics , vol.61 , pp. 335-343
    • Braun, T.M.1    Yuan, Z.2    Thall, P.F.3
  • 6
    • 0034877849 scopus 로고    scopus 로고
    • A bivariate cure-mixture approach for modeling familial association in diseases
    • Chatterjee, N. Shih, J. (2001) A bivariate cure-mixture approach for modeling familial association in diseases. Biometrics, 57, 779 786.
    • (2001) Biometrics , vol.57 , pp. 779-786
    • Chatterjee, N.1    Shih, J.2
  • 7
    • 0033637096 scopus 로고    scopus 로고
    • Sequential designs for phase i clinical trials with late-onset toxicities
    • Cheung, Y. K. Chappell, R. (2000) Sequential designs for phase I clinical trials with late-onset toxicities. Biometrics, 56, 1177 1182.
    • (2000) Biometrics , vol.56 , pp. 1177-1182
    • Cheung, Y.K.1    Chappell, R.2
  • 8
    • 0017883262 scopus 로고
    • A model for association in bivariate life tables and its application in epidemiological studies of familial tendency in chronic disease incidence
    • Clayton, D. G. (1978) A model for association in bivariate life tables and its application in epidemiological studies of familial tendency in chronic disease incidence. Biometrika, 65, 141 151.
    • (1978) Biometrika , vol.65 , pp. 141-151
    • Clayton, D.G.1
  • 9
    • 0000336139 scopus 로고
    • Regression models and life-tables (with discussion).
    • Cox, D. R. (1972) Regression models and life-tables (with discussion). J. R. Statist. Soc. B, 34, 187 220.
    • (1972) J. R. Statist. Soc. B , vol.34 , pp. 187-220
    • Cox, D.R.1
  • 10
    • 0033979541 scopus 로고    scopus 로고
    • Effect of time to complete remission on subsequent survival and disease-free survival time in AML, RAEB-t, and RAEB
    • Estey, E. H., Shen, Y. Thall, P. F. (2000) Effect of time to complete remission on subsequent survival and disease-free survival time in AML, RAEB-t, and RAEB. Blood, 95, 72 77.
    • (2000) Blood , vol.95 , pp. 72-77
    • Estey, E.H.1    Shen, Y.2    Thall, P.F.3
  • 11
    • 0033918775 scopus 로고    scopus 로고
    • A curve-free method for phase i clinical trials
    • Gasparini, M. Eisele, J. (2000) A curve-free method for phase I clinical trials. Biometrics, 56, 609 615.
    • (2000) Biometrics , vol.56 , pp. 609-615
    • Gasparini, M.1    Eisele, J.2
  • 12
    • 0038312668 scopus 로고
    • Adaptive rejection Metropolis sampling within Gibbs sampling
    • Gilks, W. R., Best, N. G. Tan, K. K. C. (1995) Adaptive rejection Metropolis sampling within Gibbs sampling. Appl. Statist., 44, 455 472.
    • (1995) Appl. Statist. , vol.44 , pp. 455-472
    • Gilks, W.R.1    Best, N.G.2    Tan, K.K.C.3
  • 13
    • 0029027770 scopus 로고
    • Some practical improvements in the continual reassessment method for phase i studies
    • Goodman, S. N., Zahurak, M. L. Piantadosi, S. (1995) Some practical improvements in the continual reassessment method for phase I studies. Statist. Med., 14, 1149 1161.
    • (1995) Statist. Med. , vol.14 , pp. 1149-1161
    • Goodman, S.N.1    Zahurak, M.L.2    Piantadosi, S.3
  • 15
    • 0001356210 scopus 로고
    • A mixture model combining logistic regression with proportional hazards regression
    • Kuk, A. Y. C. Chen, C. H. (1992) A mixture model combining logistic regression with proportional hazards regression. Biometrika, 79, 531 541.
    • (1992) Biometrika , vol.79 , pp. 531-541
    • Kuk, A.Y.C.1    Chen, C.H.2
  • 16
    • 0037080851 scopus 로고    scopus 로고
    • An extension of the continual reassessment method using decision theory
    • Leung, D. H.-Y. Wang, Y.-G. (2002) An extension of the continual reassessment method using decision theory. Statist. Med., 21, 51 63.
    • (2002) Statist. Med. , vol.21 , pp. 51-63
    • Leung, D.H.-Y.1    Wang, Y.-G.2
  • 18
    • 0029001313 scopus 로고
    • An extension of the continual reassessment methods using a preliminary up-and-down design in a dose finding study in cancer patients, in order to investigate a greater range of doses
    • Møller, S. (1995) An extension of the continual reassessment methods using a preliminary up-and-down design in a dose finding study in cancer patients, in order to investigate a greater range of doses. Statist. Med., 14, 911 922.
    • (1995) Statist. Med. , vol.14 , pp. 911-922
    • Møller, S.1
  • 19
    • 0034019219 scopus 로고    scopus 로고
    • Bayesian nonparametric inference on the dose level with specified response rate
    • Mukhopadhyay, S. (2000) Bayesian nonparametric inference on the dose level with specified response rate. Biometrics, 56, 220 226.
    • (2000) Biometrics , vol.56 , pp. 220-226
    • Mukhopadhyay, S.1
  • 20
    • 0025148278 scopus 로고
    • Continual reassessment method: A practical design for Phase 1 clinical trials in cancer
    • O'Quigley, J., Pepe, M. Fisher, L. (1990) Continual reassessment method: a practical design for Phase 1 clinical trials in cancer. Biometrics, 46, 33 48.
    • (1990) Biometrics , vol.46 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 21
    • 0024452804 scopus 로고
    • Design and analysis of Phase i clinical trials
    • Storer, B. E. (1989) Design and analysis of Phase I clinical trials. Biometrics, 45, 925 937.
    • (1989) Biometrics , vol.45 , pp. 925-937
    • Storer, B.E.1
  • 22
    • 4444272419 scopus 로고    scopus 로고
    • Dose-finding based on toxicity-efficacy trade-offs
    • Thall, P. F. Cook, J. (2004) Dose-finding based on toxicity-efficacy trade-offs. Biometrics, 60, 684 693.
    • (2004) Biometrics , vol.60 , pp. 684-693
    • Thall, P.F.1    Cook, J.2
  • 23
    • 33748795036 scopus 로고    scopus 로고
    • Bayesian dose-finding in phase I/II trials using toxicity and efficacy odds ratio
    • Yin, G., Li, Y. Ji, Y. (2006) Bayesian dose-finding in phase I/II trials using toxicity and efficacy odds ratio. Biometrics, 62, 777 784.
    • (2006) Biometrics , vol.62 , pp. 777-784
    • Yin, G.1    Li, Y.2    Ji, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.