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Volumn 25, Issue 12, 2006, Pages 2027-2042

A model-based approach in the estimation of the maximum tolerated dose in phase I cancer clinical trials

Author keywords

Dose limiting toxicity; Maximum tolerated dose; Model based approach; Traditional 3+3 designs; Traditional algorithm based designs

Indexed keywords

ANTINEOPLASTIC AGENT;

EID: 33745453653     PISSN: 02776715     EISSN: 10970258     Source Type: Journal    
DOI: 10.1002/sim.2334     Document Type: Article
Times cited : (29)

References (18)
  • 2
    • 0030044379 scopus 로고    scopus 로고
    • Design and results of phase I cancer clinical trials: Three-year experience at M.D. Anderson Cancer Center
    • Smith T, Lee J, Kantarjian H, Legha S, Rober M. Design and results of phase I cancer clinical trials: three-year experience at M.D. Anderson Cancer Center. Journal of Clinical Oncology 1996; 14(1):287-295.
    • (1996) Journal of Clinical Oncology , vol.14 , Issue.1 , pp. 287-295
    • Smith, T.1    Lee, J.2    Kantarjian, H.3    Legha, S.4    Rober, M.5
  • 3
    • 0008707207 scopus 로고    scopus 로고
    • Overview of phase I trials
    • Crowley (ed.). Marcel Dekker: New York
    • Edler L. Overview of phase I trials. In Handbook of Statistics in Clinical Oncology, Crowley (ed.). Marcel Dekker: New York, 2001; 1-34.
    • (2001) Handbook of Statistics in Clinical Oncology , pp. 1-34
    • Edler, L.1
  • 4
    • 0025148278 scopus 로고
    • Continual reassessment method: A practical design for phase I clinical studies in cancer
    • O'Quigley J, Pepe M, Fisher L. Continual reassessment method: a practical design for phase I clinical studies in cancer. Biometrics 1990; 46:33-48.
    • (1990) Biometrics , vol.46 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 5
    • 0030993031 scopus 로고    scopus 로고
    • A random walk rule for phase I clinical trials
    • Durham S, Flournoy N, Rosenberger W. A random walk rule for phase I clinical trials. Biometrics 1997; 53:745-760.
    • (1997) Biometrics , vol.53 , pp. 745-760
    • Durham, S.1    Flournoy, N.2    Rosenberger, W.3
  • 6
    • 0029071328 scopus 로고
    • Bayesian decision procedures for dose determining experiments
    • Whitehead J, Brunier H. Bayesian decision procedures for dose determining experiments. Statistics in Medicine 1995; 14:885-893.
    • (1995) Statistics in Medicine , vol.14 , pp. 885-893
    • Whitehead, J.1    Brunier, H.2
  • 7
    • 0030848713 scopus 로고    scopus 로고
    • Bayesian decision procedures with application to dose-finding studies
    • Whitehead J. Bayesian decision procedures with application to dose-finding studies. International Journal of Pharmaceutical Medicine 1997; 11:201-208.
    • (1997) International Journal of Pharmaceutical Medicine , vol.11 , pp. 201-208
    • Whitehead, J.1
  • 8
    • 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; 17:1103-1120.
    • (1998) Statistics in Medicine , vol.17 , pp. 1103-1120
    • Babb, J.1    Rogatko, A.2    Zacks, S.3
  • 9
    • 0035739843 scopus 로고    scopus 로고
    • The expected toxicity rate at the maximum tolerated dose in the standard phase I cancer clinical trial design
    • Kang S, Ahn C. The expected toxicity rate at the maximum tolerated dose in the standard phase I cancer clinical trial design. Drug Information Journal 2001; 35:1189-1199.
    • (2001) Drug Information Journal , vol.35 , pp. 1189-1199
    • Kang, S.1    Ahn, C.2
  • 10
    • 0036975813 scopus 로고    scopus 로고
    • An investigation of the traditional algorithm-based designs for phase I cancer clinical trials
    • Kang S, Ahn C. An investigation of the traditional algorithm-based designs for phase I cancer clinical trials. Drug Information Journal 2002; 36:865-873.
    • (2002) Drug Information Journal , vol.36 , pp. 865-873
    • Kang, S.1    Ahn, C.2
  • 11
    • 0012957270 scopus 로고    scopus 로고
    • Statistical properties of the traditional algorithm-based designs for phase I cancer clinical trials
    • Lin Y, Shih WJ. Statistical properties of the traditional algorithm-based designs for phase I cancer clinical trials. Biostatistics 2001; 2(2):203-215.
    • (2001) Biostatistics , vol.2 , Issue.2 , pp. 203-215
    • Lin, Y.1    Shih, W.J.2
  • 14
    • 0024452804 scopus 로고
    • Design and analysis of phase I clinical trials
    • Storer B. Design and analysis of phase I clinical trials. Biometrics 1989; 45:925-937.
    • (1989) Biometrics , vol.45 , pp. 925-937
    • Storer, B.1
  • 15
    • 0037201011 scopus 로고    scopus 로고
    • Competing designs for phase I clinical trials: A review
    • Rosenberger W, Haines L. Competing designs for phase I clinical trials: a review. Statistics in Medicine 2002; 21:2757-2770.
    • (2002) Statistics in Medicine , vol.21 , pp. 2757-2770
    • Rosenberger, W.1    Haines, L.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
    • 0025986460 scopus 로고
    • Methods for dose finding studies in cancer trials: A review and results of a Monte Carlo study
    • O'Quigley J, Chevret S. Methods for dose finding studies in cancer trials: a review and results of a Monte Carlo study. Statistics in Medicine 1991; 10:1647-1664.
    • (1991) Statistics in Medicine , vol.10 , pp. 1647-1664
    • O'Quigley, J.1    Chevret, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.