-
1
-
-
77953010578
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
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
-
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
-
19
-
-
0030749549
-
Accelerated titration designs for phase I clinical trials in oncology
-
SIMON, R., FREIDLIN, B., RUBINSTEIN, L., ARBUCK, S. G., COLLINS, J. AND CHRISTIAN, M. C. (1997). Accelerated titration designs for phase I clinical trials in oncology. Journal of the National Cancer Institute 89, 1138-1147. (Pubitemid 27337928)
-
(1997)
Journal of the National Cancer Institute
, vol.89
, Issue.15
, pp. 1138-1147
-
-
Simon, R.1
Freidlin, B.2
Rubinstein, L.3
Arbuck, S.G.4
Collins, J.5
Christian, M.C.6
-
20
-
-
34247276015
-
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
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