메뉴 건너뛰기




Volumn 12, Issue 2, 2011, Pages 386-398

Continual reassessment method with multiple toxicity constraints

Author keywords

Design calibration; Dose finding cancer trials; Toxicity grades and types

Indexed keywords

ANTINEOPLASTIC AGENT; BORONIC ACID DERIVATIVE; BORTEZOMIB; CYCLOPHOSPHAMIDE; DOXORUBICIN; PREDNISOLONE; PYRAZINE DERIVATIVE; VINCRISTINE;

EID: 79953141091     PISSN: 14654644     EISSN: 14684357     Source Type: Journal    
DOI: 10.1093/biostatistics/kxq062     Document Type: Article
Times cited : (45)

References (20)
  • 1
    • 77953010578 scopus 로고    scopus 로고
    • Risk-group-specifc dose fnding based on an average toxicity score
    • BEKELE, B. N., LI, Y. AND JI, Y. (2009). Risk-group-specifc dose fnding based on an average toxicity score. Biometrics 66, 541-548.
    • (2009) Biometrics , vol.66 , pp. 541-548
    • Bekele, B.N.1    Y, L.I.2    Y, J.I.3
  • 2
    • 2142670647 scopus 로고    scopus 로고
    • Dose-Finding Based on Multiple Toxicities in a Soft Tissue Sarcoma Trial
    • BEKELE, B. N. AND THALL, P. (2004). Dose-fnding based on multiple toxicities in a soft tissue sarcoma trial. Journal of the American Statistical Association 99, 26-35. (Pubitemid 38545191)
    • (2004) Journal of the American Statistical Association , vol.99 , Issue.465 , pp. 26-35
    • Bekele, B.N.1    Thall, P.F.2
  • 3
    • 0036188788 scopus 로고    scopus 로고
    • On the use of nonparametric curves in phase I trials with low toxicity tolerance
    • CHEUNG, Y. K. (2002). On the use of non-parametric curves in phase I trials with low toxicity tolerance. Biometrics 58, 237-240. (Pubitemid 34194510)
    • (2002) Biometrics , vol.58 , Issue.1 , pp. 237-240
    • Cheung, Y.K.1
  • 4
    • 27944494441 scopus 로고    scopus 로고
    • Coherence principles in dose-fnding studies
    • CHEUNG, Y. K. (2005). Coherence principles in dose-fnding studies. Biometrika 92, 863-873.
    • (2005) Biometrika , vol.92 , pp. 863-873
    • Cheung, Y.K.1
  • 5
    • 38349062295 scopus 로고    scopus 로고
    • Sequential implementation of stepwise procedures for identifying the maximum tolerated dose
    • CHEUNG, Y. K. (2007). Sequential implementation of stepwise procedures for identifying the maximum tolerated dose. Journal of the American Statistical Association 102, 1448-1461.
    • (2007) Journal of the American Statistical Association , vol.102 , pp. 1448-1461
    • Cheung, Y.K.1
  • 6
    • 0036712359 scopus 로고    scopus 로고
    • A simple technique to evaluate model sensitivity in the continual reassessment method
    • CHEUNG, Y. K. AND CHAPPELL, R. (2002). A simple technique to evaluate model sensitivity in the continual reassessment method. Biometrics 58, 671-674. (Pubitemid 35001486)
    • (2002) Biometrics , vol.58 , Issue.3 , pp. 671-674
    • Cheung, Y.K.1    Chappell, R.2
  • 7
    • 77249122114 scopus 로고    scopus 로고
    • Stochastic approximation with virtual observations for dose-fnding on discrete levels
    • CHEUNG, Y. K. AND ELKIND, M. S. V. (2010). Stochastic approximation with virtual observations for dose-fnding on discrete levels. Biometrika 97, 109-121.
    • (2010) Biometrika , vol.97 , pp. 109-121
    • Cheung, Y.K.1    Elkind, M.S.V.2
  • 8
    • 0030993031 scopus 로고    scopus 로고
    • A random walk rule for phase I clinical trials
    • DOI 10.2307/2533975
    • DURHAM, S. D., FLOURNOY, N. AND ROSENBERGER, W. (1997). A random walk rule for phase I clinical trials. Biometrics 53, 745-760. (Pubitemid 27262236)
    • (1997) Biometrics , vol.53 , Issue.2 , pp. 745-760
    • Durham, S.D.1    Flournoy, N.2    Rosenberger, W.F.3
  • 10
    • 0029027770 scopus 로고
    • Some practical improvements in the continual reassessment method for phase i studies
    • GOODMAN, S. N., ZAHURAK, M. L. AND PIANTADOSI, S. (1995). Some practical improvements in the continual reassessment method for phase I studies. Statistics in Medicine 14, 1149-1161.
    • (1995) Statistics in Medicine , vol.14 , pp. 1149-1161
    • Goodman, S.N.1    Zahurak, M.L.2    Piantadosi, S.3
  • 11
    • 60749092627 scopus 로고    scopus 로고
    • Dose fnding for continuous and ordinal outcomes with a monotone objective function: A unifed approach
    • IVANOVA, A. AND KIM, S. H. (2009). Dose fnding for continuous and ordinal outcomes with a monotone objective function: a unifed approach. Biometrics 65, 247-255.
    • (2009) Biometrics , vol.65 , pp. 247-255
    • Ivanova, A.1    Kim, S.H.2
  • 12
    • 34548619360 scopus 로고    scopus 로고
    • Dose-fnding in phase i clinical trials based on toxicity probability intervals
    • JI, Y., LI, Y. AND BEKELE, N. (2007). Dose-fnding in phase I clinical trials based on toxicity probability intervals. Clinical Trials 4, 235-244.
    • (2007) Clinical Trials , vol.4 , pp. 235-244
    • Y, J.I.1    Y, L.I.2    Bekele, N.3
  • 13
    • 67649321803 scopus 로고    scopus 로고
    • Model calibration in the continual reassessment method
    • LEE, S. M. AND CHEUNG, Y. K. (2009). Model calibration in the continual reassessment method. Clinical Trials 6, 227-238.
    • (2009) Clinical Trials , vol.6 , pp. 227-238
    • Lee, S.M.1    Cheung, Y.K.2
  • 14
    • 84858252858 scopus 로고    scopus 로고
    • Validation of toxicity burden score for use in phase i clinical trials
    • (abstr. 2514)
    • LEE, S. M., HERSHMAN, D., MARTIN, P., LEONARD, K. AND CHEUNG, Y. K. (2009). Validation of toxicity burden score for use in phase I clinical trials. Journal of Clinical Oncology 27 (Suppl.), 15s (abstr. 2514).
    • (2009) Journal of Clinical Oncology , vol.27 , Issue.SUPPL.
    • Lee, S.M.1    Hershman, D.2    Martin, P.3    Leonard, K.4    Cheung, Y.K.5
  • 15
    • 33745892167 scopus 로고    scopus 로고
    • Phase I/II trial of bortezomib plus CHOP-Rituximab in diffuse large B cell (DLBCL) and mantle cell lymphona (MCL): Phase i results
    • and others (abstr. 491)
    • LEONARD, J. P., FURMAN, R. R., CHEUNG, Y. K. K., FELDMAN, E. J., CHO, H. J., VOSE, J. M., NICHOLS, G., GLYNN, P. W., JOYCE, M. A., KETAS, J. and others (2005). Phase I/II trial of bortezomib plus CHOP-Rituximab in diffuse large B cell (DLBCL) and mantle cell lymphona (MCL): phase I results. Blood 106, 147a (abstr. 491).
    • (2005) Blood , vol.106
    • Leonard, J.P.1    Furman, R.R.2    Cheung, Y.K.K.3    Feldman, E.J.4    Cho, H.J.5    Vose, J.M.6    Nichols, G.7    Glynn, P.W.8    Joyce, M.A.9    Ketas, J.10
  • 16
    • 0006407254 scopus 로고    scopus 로고
    • WinBUGS-a Bayesian modelling framework: Concepts, structure, and extensibility
    • LUNN, D. J., THOMAS, A., BEST, N. AND SPIEGELHALTER, D. (2000). WinBUGS-a Bayesian modelling framework: concepts, structure, and extensibility. Statistics and Computing 10, 325-337.
    • (2000) Statistics and Computing , vol.10 , pp. 325-337
    • Lunn, D.J.1    Thomas, A.2    Best, N.3    Spiegelhalter, D.4
  • 17
    • 12344312699 scopus 로고    scopus 로고
    • NATIONAL CANCER INSTITUTE CTCAEi Version 3.0. Bethesda: National Cancer Institute.
    • NATIONAL CANCER INSTITUTE (2003). Common Terminology Criteria for Adverse Events (CTCAE). Version 3.0. Bethesda: National Cancer Institute. http://ctep.cancer.gov/forms/CTCAEv3.pdf.
    • (2003) Common Terminology Criteria for Adverse Events
  • 18
    • 0025148278 scopus 로고
    • Continual reassessment method: A practical design for phase 1 clinical trials in cancer
    • DOI 10.2307/2531628
    • O'QUIGLEY, J., PEPE, M. AND FISHER, L. (1990). Continual reassessment method: a practical design for phase I clinical trials in cancer. Biometrics 46, 33-48. (Pubitemid 20245604)
    • (1990) Biometrics , vol.46 , Issue.1 , pp. 33-48
    • O'Quigley, J.1    Pepe, M.2    Fisher, L.3
  • 20
    • 34247276015 scopus 로고    scopus 로고
    • The continual reassessment method for multiple toxicity grades: A Bayesian quasi-likelihood approach
    • YUAN, Z., CHAPPELL, R. AND BAILEY, H. (2007). The continual reassessment method for multiple toxicity grades: a Bayesian quasi-likelihood approach. Biometrics 63, 173-179.
    • (2007) Biometrics , vol.63 , pp. 173-179
    • Yuan, Z.1    Chappell, R.2    Bailey, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.