메뉴 건너뛰기




Volumn 38, Issue 3, 1998, Pages 215-220

Optimal Bayesian-feasible dose escalation for cancer phase I trials

Author keywords

Bayesian adaptive procedure; Bayesian feasible scheme; Cancer phase I clinical trials; Consistent escalation scheme; Constrained optimization; Dose escalation scheme

Indexed keywords


EID: 0032525496     PISSN: 01677152     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0167-7152(98)00016-9     Document Type: Article
Times cited : (38)

References (10)
  • 1
    • 0010068276 scopus 로고    scopus 로고
    • Cancer phase I clinical trials: Efficient dose escalation with overdose control
    • in press
    • Babb, J., Rogatko, A., Zacks, S., 1997. Cancer Phase I Clinical Trials: Efficient Dose Escalation With Overdose Control, Statistics in Medicine (in press).
    • (1997) Statistics in Medicine
    • Babb, J.1    Rogatko, A.2    Zacks, S.3
  • 3
    • 0026663871 scopus 로고
    • Bayesian methods for phase I clinical trials
    • Gastonis, C., Greenhouse, J.B., 1992. Bayesian methods for Phase I Clinical Trials. Statist. Med. 11, 1377-1389.
    • (1992) Statist. Med. , vol.11 , pp. 1377-1389
    • Gastonis, C.1    Greenhouse, J.B.2
  • 4
    • 0025148278 scopus 로고
    • Continual reassessment method: A practical design for phase I clinical trials in cancer
    • O'Quigley, J., Pepe, M., Fisher, L., 1990. Continual reassessment method: a practical design for Phase I clinical trials in cancer. Biometrics 46, 33-38.
    • (1990) Biometrics , vol.46 , pp. 33-38
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 5
    • 0025986460 scopus 로고
    • Methods for dose finding studies in cancer clinical trials: A review and result of Monte Carlo study
    • O'Quigley, J., Chevret, S., 1991. Methods for dose finding studies in cancer clinical trials: A review and result of Monte Carlo study. Statist. Med. 10, 1047-1664.
    • (1991) Statist. Med. , vol.10 , pp. 1047-1664
    • O'Quigley, J.1    Chevret, S.2
  • 7
    • 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
  • 8
    • 0002871130 scopus 로고
    • Selection of dose levels for estimating a percentage point of a logistic quantal response curve
    • Tsutakawa, R.K., 1980. Selection of dose levels for estimating a percentage point of a logistic quantal response curve. J. Roy. Statist. Soc. Ser. C 29, 25-33.
    • (1980) J. Roy. Statist. Soc. Ser. C , vol.29 , pp. 25-33
    • Tsutakawa, R.K.1
  • 9
    • 70350337921 scopus 로고    scopus 로고
    • Adaptive designs for parametric models
    • Chapter 5. Elsevier, Amsterdam
    • Zacks, S., 1996. Adaptive designs for parametric models. In: Handbook of Statistics, vol. 13, Chapter 5. Elsevier, Amsterdam.
    • (1996) Handbook of Statistics , vol.13
    • Zacks, S.1
  • 10
    • 70350322540 scopus 로고
    • Sequential search of optimal dosages: The linear regression case
    • North-Holland, Amsterdam
    • Zacks, S., Eichhorn, B.H., 1975. Sequential search of optimal dosages: The linear regression case. In: Statistical Design and Linear Models. North-Holland, Amsterdam.
    • (1975) Statistical Design and Linear Models
    • Zacks, S.1    Eichhorn, B.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.