-
1
-
-
0031920799
-
Cancer phase i clinical trials: Efficient dose escalation with overdose control
-
Babb, J., Rogatko, A., Zacks, S. (1997). Cancer phase I clinical trials: efficient dose escalation with overdose control. Statistics in Medicine 11:1103-1120.
-
(1997)
Statistics in Medicine
, vol.11
, pp. 1103-1120
-
-
Babb, J.1
Rogatko, A.2
Zacks, S.3
-
2
-
-
20744435134
-
A Bayesian approach to jointly modeling toxicity and biomarker expression in a phase I/II dose-finding trial
-
Bekele, B., Shen, Y. (2005). A Bayesian approach to jointly modeling toxicity and biomarker expression in a phase I/II dose-finding trial. Biometrics 61:344-354.
-
(2005)
Biometrics
, vol.61
, pp. 344-354
-
-
Bekele, B.1
Shen, Y.2
-
3
-
-
0036277621
-
The bivariate continual reassessment method: Extending the CRM to phase i trials of two competing outcomes
-
Braun, T. (2002). The bivariate continual reassessment method: Extending the CRM to phase I trials of two competing outcomes. Controlled Clinical Trials 23:240-256.
-
(2002)
Controlled Clinical Trials
, vol.23
, pp. 240-256
-
-
Braun, T.1
-
4
-
-
0029591692
-
Incorporating toxicity considerations into the design of two-stage phase II clinical trials
-
Bryant, J., Day, R. (1995). Incorporating toxicity considerations into the design of two-stage phase II clinical trials. Biometrics 51:1372-1383.
-
(1995)
Biometrics
, vol.51
, pp. 1372-1383
-
-
Bryant, J.1
Day, R.2
-
5
-
-
32044450843
-
Adaptive designs for dose-finding based on efficacy toxicity response
-
Dragalin, V., Fedorov, V. (2006). Adaptive designs for dose-finding based on efficacy toxicity response. Journal of Statistical Planning and Inference 136(6):1800-1823.
-
(2006)
Journal of Statistical Planning and Inference
, vol.136
, Issue.6
, pp. 1800-1823
-
-
Dragalin, V.1
Fedorov, V.2
-
6
-
-
60249094068
-
Two-stage design for dose-finding that accounts for both efficacy and safety
-
Dragalin, V., Fedorov, V., Wu, Y. (2008). Two-stage design for dose-finding that accounts for both efficacy and safety. Statistics in Medicine 27(25):5156-5176.
-
(2008)
Statistics in Medicine
, vol.27
, Issue.25
, pp. 5156-5176
-
-
Dragalin, V.1
Fedorov, V.2
Wu, Y.3
-
7
-
-
0035810147
-
Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia
-
Druker, B., Talpaz, M., Resta, D., Peng, B., Buchdunger, E., Ford, J. M., Lydon, N. B., Kantarjian, H., Capdeville, R., Ohno-Jones, S., Sawyers, C. L. (2001). Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. The New England Journal of Medicine 344(14):1031-1037.
-
(2001)
The New England Journal of Medicine
, vol.344
, Issue.14
, pp. 1031-1037
-
-
Druker, B.1
Talpaz, M.2
Resta, D.3
Peng, B.4
Buchdunger, E.5
Ford, J.M.6
Lydon, N.B.7
Kantarjian, H.8
Capdeville, R.9
Ohno-Jones, S.10
Sawyers, C.L.11
-
8
-
-
33845444046
-
IRIS investigators. Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia
-
Druker, B. J., Guilhot, F., O'Brien, S. G., Gathmann, I., Kantarjian, H., Gattermann, N., Deininger, M. W., Silver, R. T., Goldman, J. M., Stone, R. M., Cervantes, F., Hochhaus, A., Powell, B. L., Gabrilove, J. L., Rousselot, P., Reiffers, J., Cornelissen, J. J., Hughes, T., Agis, H., Fischer, T., Verhoef, G., Shepherd, J., Saglio, G., Gratwohl, A., Nielsen, J. L., Radich, J. P., Simonsson, B., Taylor, K., Baccarani, M., So, C., Letvak, L., Larson, R. A. (2006). IRIS investigators. Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. New England Journal of Medicine 355(23):2408-2417.
-
(2006)
New England Journal of Medicine
, vol.355
, Issue.23
, pp. 2408-2417
-
-
Druker, B.J.1
Guilhot, F.2
O'Brien, S.G.3
Gathmann, I.4
Kantarjian, H.5
Gattermann, N.6
Deininger, M.W.7
Silver, R.T.8
Goldman, J.M.9
Stone, R.M.10
Cervantes, F.11
Hochhaus, A.12
Powell, B.L.13
Gabrilove, J.L.14
Rousselot, P.15
Reiffers, J.16
Cornelissen, J.J.17
Hughes, T.18
Agis, H.19
Fischer, T.20
Verhoef, G.21
Shepherd, J.22
Saglio, G.23
Gratwohl, A.24
Nielsen, J.L.25
Radich, J.P.26
Simonsson, B.27
Taylor, K.28
Baccarani, M.29
So, C.30
Letvak, L.31
Larson, R.A.32
more..
-
9
-
-
0030993031
-
A random walk rule for phase i clinical trials
-
Durham, S., Flournoy, N., Rosenberger, W. (1997). A random walk rule for phase I clinical trials. Biometrics 53:745-760.
-
(1997)
Biometrics
, vol.53
, pp. 745-760
-
-
Durham, S.1
Flournoy, N.2
Rosenberger, W.3
-
10
-
-
0025837127
-
Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferasedeficient child with acute lymphoblastic leukemia
-
Evans, W., Horner, M., Chu, Y., Kalwinsky, D., Roberts, W. (1991). Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferasedeficient child with acute lymphoblastic leukemia. Journal of Pediatrics 119:985-989.
-
(1991)
Journal of Pediatrics
, vol.119
, pp. 985-989
-
-
Evans, W.1
Horner, M.2
Chu, Y.3
Kalwinsky, D.4
Roberts, W.5
-
11
-
-
0033918775
-
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
-
-
0029027770
-
Some practical improvments in the continual reassessment method for phase i studies
-
Goodman, S., Zahurak, M., Piantadosi, S. (1995). Some practical improvments 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.1
Zahurak, M.2
Piantadosi, S.3
-
13
-
-
0027949027
-
Simulation as a design tool for phase I/II clinical trials: An example from bone marrow transplantation
-
Gooley, T., Martin, P., Fisher, L., Pettinger, M. (1994). Simulation as a design tool for phase I/II clinical trials: an example from bone marrow transplantation. Controlled Clinical trials 15:450-462.
-
(1994)
Controlled Clinical Trials
, vol.15
, pp. 450-462
-
-
Gooley, T.1
Martin, P.2
Fisher, L.3
Pettinger, M.4
-
14
-
-
0041333015
-
Bayesian optimal designs for phase i clinical trials
-
Haines, L., Perevoszkaya, I., Rosenberger, W. (2003). Bayesian optimal designs for phase I clinical trials. Biometrics 59:591-600.
-
(2003)
Biometrics
, vol.59
, pp. 591-600
-
-
Haines, L.1
Perevoszkaya, I.2
Rosenberger, W.3
-
15
-
-
0037438434
-
Improved up-anddown designs for phase i trials
-
Ivanova, A., Montazer-Haghighi, A., Mohanty, S., Durham, S. (2003). Improved up-anddown designs for phase I trials. Statistics in Medicine 22:69-82.
-
(2003)
Statistics in Medicine
, vol.22
, pp. 69-82
-
-
Ivanova, A.1
Montazer-Haghighi, A.2
Mohanty, S.3
Durham, S.4
-
16
-
-
0028170238
-
A comparison of two phase i designs
-
Korn, E., Midthune, D., Chen, T., Rubinstein, L., Christian, M., Simon, R. (1994). A comparison of two phase I designs. Statistics in Medicine 13:1799-1806.
-
(1994)
Statistics in Medicine
, vol.13
, pp. 1799-1806
-
-
Korn, E.1
Midthune, D.2
Chen, T.3
Rubinstein, L.4
Christian, M.5
Simon, R.6
-
17
-
-
0030802914
-
Thiopurine methyltransferase deficiency in childhood lymphoblastic leukemia: 6-mercaptopurine dosage strategies
-
Lennard, L., Lewis, I., Michelagnoli, M., Lilleyman, J. (1997). Thiopurine methyltransferase deficiency in childhood lymphoblastic leukemia: 6-mercaptopurine dosage strategies. Medical and Pediatric Oncology 29:252-255.
-
(1997)
Medical and Pediatric Oncology
, vol.29
, pp. 252-255
-
-
Lennard, L.1
Lewis, I.2
Michelagnoli, M.3
Lilleyman, J.4
-
18
-
-
0035075179
-
Isotonic designs for phase i trials
-
Leung, D., Wang, Y. (2001). Isotonic designs for phase I trials. Controlled Clinical Trials 22:126-138.
-
(2001)
Controlled Clinical Trials
, vol.22
, pp. 126-138
-
-
Leung, D.1
Wang, Y.2
-
19
-
-
31344433744
-
A Bayesian dose finding design for dual endpoint phase i trials
-
Loke, Y., Tan, S., Cai, Y., Machin, D. (2006). A Bayesian dose finding design for dual endpoint phase I trials. Statistics in Medicine 25:3-22.
-
(2006)
Statistics in Medicine
, vol.25
, pp. 3-22
-
-
Loke, Y.1
Tan, S.2
Cai, Y.3
MacHin, D.4
-
20
-
-
0029001313
-
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
-
Moller, 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. Statistics in Medicine 14:911-922.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 911-922
-
-
Moller, S.1
-
21
-
-
0029938415
-
Continual reassessment method: A likelihood approach
-
O'Quigley, J., Shen, L. Z. (1996). Continual reassessment method: a likelihood approach. Biometrics 52:673-684.
-
(1996)
Biometrics
, vol.52
, pp. 673-684
-
-
O'Quigley, J.1
Shen, L.Z.2
-
22
-
-
0025148278
-
Continual reassessment method: A practical design for phase i clinical trials in cancer
-
O'Quigley, J., Pepe, M., Fisher, M. (1990). Continual reassessment method: a practical design for phase I clinical trials in cancer. Biometrics 46:33-48.
-
(1990)
Biometrics
, vol.46
, pp. 33-48
-
-
O'Quigley, J.1
Pepe, M.2
Fisher, M.3
-
23
-
-
0035186085
-
Dose-finding designs for HIV studies
-
O'Quigley, J., Hughes, M., Fenton, T. (2001). Dose-finding designs for HIV studies. Biometrics 57:1018-1029.
-
(2001)
Biometrics
, vol.57
, pp. 1018-1029
-
-
O'Quigley, J.1
Hughes, M.2
Fenton, T.3
-
24
-
-
0037100229
-
Adaptive dose finding for phase i clinical trials of drugs used for chemotherapy of cancer
-
Potter, D. (2002). Adaptive dose finding for phase I clinical trials of drugs used for chemotherapy of cancer. Statistics in Medicine 21:1805-1823.
-
(2002)
Statistics in Medicine
, vol.21
, pp. 1805-1823
-
-
Potter, D.1
-
26
-
-
0033486029
-
Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus
-
Relling, M., Hancock, M., Rivera, G., Sundlund, J., Ribeiro, R., Krynetski, E., Pui, C. H., Evans, W. (1999). Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus. Journal of the National Cancer Institute 91:2001-2008.
-
(1999)
Journal of the National Cancer Institute
, vol.91
, pp. 2001-2008
-
-
Relling, M.1
Hancock, M.2
Rivera, G.3
Sundlund, J.4
Ribeiro, R.5
Krynetski, E.6
Pui, C.H.7
Evans, W.8
-
27
-
-
36849035490
-
Translation of innovative designs into phase i trials
-
Rogatko, A., Schoeneck, D., Jonas, W., Tighiouart, M., Khuri, F. R., Porter, A. (2007). Translation of innovative designs into phase I trials. Journal of Clinical Oncology 25(31):4982-4986.
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.31
, pp. 4982-4986
-
-
Rogatko, A.1
Schoeneck, D.2
Jonas, W.3
Tighiouart, M.4
Khuri, F.R.5
Porter, A.6
-
28
-
-
0030749549
-
Accelerated titration designs for phase i clinical trials in oncology
-
Simon, R., Freidlin, B., Rubinstein, L., Arbuck, S., Collins, J., Christian, M. (1997). Accelerated titration designs for phase I clinical trials in oncology. Journal of the National Cancer Institute 89:1138-1147.
-
(1997)
Journal of the National Cancer Institute
, vol.89
, pp. 1138-1147
-
-
Simon, R.1
Freidlin, B.2
Rubinstein, L.3
Arbuck, S.4
Collins, J.5
Christian, M.6
-
29
-
-
0038545822
-
Decision-theoretic design for phase II clinical trials allowing for competing studies
-
Stallard, N. (2003). Decision-theoretic design for phase II clinical trials allowing for competing studies. Biometrics 59:402-409.
-
(2003)
Biometrics
, vol.59
, pp. 402-409
-
-
Stallard, N.1
-
30
-
-
0024452804
-
Design and analysis of phase i clinical trials
-
Storer, B. (1989). Design and analysis of phase I clinical trials. Biometrics 45:925-937.
-
(1989)
Biometrics
, vol.45
, pp. 925-937
-
-
Storer, B.1
-
31
-
-
0031953966
-
A strategy for dose-finding and safety monitoring based on efficacy and adverse outcomes in phase I/II clinical trials
-
Thall, P., Russell, K. (1998). A strategy for dose-finding and safety monitoring based on efficacy and adverse outcomes in phase I/II clinical trials. Biometrics 54:251-264.
-
(1998)
Biometrics
, vol.54
, pp. 251-264
-
-
Thall, P.1
Russell, K.2
-
32
-
-
0032794987
-
A new statistical method for dose-finding based on efficacy and toxicity in early phase clinical trials
-
Thall, P., Estey, E., Sung, H. (1999). A new statistical method for dose-finding based on efficacy and toxicity in early phase clinical trials. Investigational New Drugs 17:155-167.
-
(1999)
Investigational New Drugs
, vol.17
, pp. 155-167
-
-
Thall, P.1
Estey, E.2
Sung, H.3
-
33
-
-
4444272419
-
Dose-finding based on efficacy-toxicity trade-offs
-
Thall, P., Cook, J. (2004). Dose-finding based on efficacy-toxicity trade-offs. Biometrics 60:684-693.
-
(2004)
Biometrics
, vol.60
, pp. 684-693
-
-
Thall, P.1
Cook, J.2
-
34
-
-
0029071328
-
Bayesian decision procedures for dose determing experiments
-
Whitehead, J., Brunier, H. (1995). Bayesian decision procedures for dose determing experiments. Statistics in Medicine 14:885-893.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 885-893
-
-
Whitehead, J.1
Brunier, H.2
-
35
-
-
33745176255
-
Bayesian decision procedures for binary and continuous bivariate dose-escalation studies
-
Zhou, Y., Whitehead, J., Bonvini, E., Stevens, J. (2006). Bayesian decision procedures for binary and continuous bivariate dose-escalation studies. Pharmaceutical Statistics 5:125-133.
-
(2006)
Pharmaceutical Statistics
, vol.5
, pp. 125-133
-
-
Zhou, Y.1
Whitehead, J.2
Bonvini, E.3
Stevens, J.4
|