-
1
-
-
0008470813
-
Experimental design for joint action
-
Abdelbasit, K. M. and Plackett, R. L. (1982). Experimental design for joint action. Biometrics 38, 171-179.
-
(1982)
Biometrics
, vol.38
, pp. 171-179
-
-
Abdelbasit, K.M.1
Plackett, R.L.2
-
2
-
-
0000501656
-
Information theory and an extension of the maximum likelihood principle
-
In: Second International Symposium on Information Theory, B. N. Petrov and F. Csaki (eds.), Budapest: Akademiai Kiado
-
Akaike, H. (1973). Information theory and an extension of the maximum likelihood principle. In: Second International Symposium on Information Theory, B. N. Petrov and F. Csaki (eds.), pp. 267-281. Budapest: Akademiai Kiado.
-
(1973)
, pp. 267-281
-
-
Akaike, H.1
-
4
-
-
0001646484
-
Cox's regression model for counting processes: A large-sample study
-
Andersen, P. K. and Gill, R. D. (1982). Cox's regression model for counting processes: A large-sample study. The Annals of Statistics 10, 1100-1120.
-
(1982)
The Annals of Statistics
, vol.10
, pp. 1100-1120
-
-
Andersen, P.K.1
Gill, R.D.2
-
5
-
-
0346880128
-
Identification of causal effects using instrumental variables (with discussion)
-
Angrist, J. D., Imbens, G. W., and Rubin, D. B. (1996). Identification of causal effects using instrumental variables (with discussion). Journal of the American Statistical Association 91,444-472.
-
(1996)
Journal of the American Statistical Association
, vol.91
, pp. 444-472
-
-
Angrist, J.D.1
Imbens, G.W.2
Rubin, D.B.3
-
7
-
-
0019617309
-
General models for the joint action of mixtures of drugs
-
Ashford, J. R. (1981). General models for the joint action of mixtures of drugs. Biometrics 37, 457-474.
-
(1981)
Biometrics
, vol.37
, pp. 457-474
-
-
Ashford, J.R.1
-
8
-
-
0031920799
-
Cancer phase I clinical trials: Efficient dose escalation with overdose control
-
Babb, J., Rogatko, A., and Zacks, S. (1998). Cancer phase I clinical trials: Efficient dose escalation with overdose control. Statistics in Medicine 17, 1103-1120.
-
(1998)
Statistics in Medicine
, vol.17
, pp. 1103-1120
-
-
Babb, J.1
Rogatko, A.2
Zacks, S.3
-
9
-
-
33847133828
-
On estimating treatment effects under noncompliance in randomized clinical trials: Are intent-to-treat or instrumental variables analyses perfect solutions?
-
Bang, H. and Davis, C. E. (2007). On estimating treatment effects under noncompliance in randomized clinical trials: Are intent-to-treat or instrumental variables analyses perfect solutions? Statistics in Medicine 26, 954-964.
-
(2007)
Statistics in Medicine
, vol.26
, pp. 954-964
-
-
Bang, H.1
Davis, C.E.2
-
10
-
-
67650652432
-
I-SPY 2: An adaptive breast cancer trial design in the setting of neoadjuvant chemotherapy
-
Barker, A. D., Sigman, C. C, Kelloff, G. J., Hylton, N. M., Berry, D. A., and Esserman, L. J. (2009). I-SPY 2: An adaptive breast cancer trial design in the setting of neoadjuvant chemotherapy. Clinical Pharmacology & Therapeutics 86,97-100.
-
(2009)
Clinical Pharmacology & Therapeutics
, vol.86
, pp. 97-100
-
-
Barker, A.D.1
Sigman, C.C.2
Kelloff, G.J.3
Hylton, N.M.4
Berry, D.A.5
Esserman, L.J.6
-
11
-
-
0003495202
-
Statistical Inference under Order Restrictions: The Theory and Application of Isotonic Regression
-
New York: Wiley
-
Barlow, R. E., Bartholomew, D. J., Bremner, J. M., and Brunk, H. D. (1972). Statistical Inference under Order Restrictions: The Theory and Application of Isotonic Regression. New York: Wiley.
-
(1972)
-
-
Barlow, R.E.1
Bartholomew, D.J.2
Bremner, J.M.3
Brunk, H.D.4
-
12
-
-
0004454219
-
Randomized allocation of treatments in sequential medical trials (with discussion)
-
Bather, J. A. (1981). Randomized allocation of treatments in sequential medical trials (with discussion). Journal of the Royal Statistical Society, Series B 43,265-292.
-
(1981)
Journal of the Royal Statistical Society, Series B
, vol.43
, pp. 265-292
-
-
Bather, J.A.1
-
13
-
-
0002812390
-
On the allocation of treatments in sequential medical trials (with discussion)
-
Bather, J. A. (1985). On the allocation of treatments in sequential medical trials (with discussion). International Statistical Review 53, 1-13.
-
(1985)
International Statistical Review
, vol.53
, pp. 1-13
-
-
Bather, J.A.1
-
14
-
-
0028619850
-
Evaluation of experiments with adaptive interim analyses
-
Bauer, P. and Könne, K. (1994). Evaluation of experiments with adaptive interim analyses. Biometrics 50, 1029-1041.
-
(1994)
Biometrics
, vol.50
, pp. 1029-1041
-
-
Bauer, P.1
Könne, K.2
-
15
-
-
45849147269
-
Monitoring late-onset toxicities in phase I trials using predicted risks
-
Bekele, B. N., Ji, Y, Shen, Y, and Thall, P. F. (2008). Monitoring late-onset toxicities in phase I trials using predicted risks. Biostatistics 9, 442-457.
-
(2008)
Biostatistics
, vol.9
, pp. 442-457
-
-
Bekele, B.N.1
Ji, Y.2
Shen, Y.3
Thall, P.F.4
-
16
-
-
20744435134
-
A Bayesian approach to jointly modeling toxicity and biomarker expression in a phase I/II dose-finding trial
-
Bekele, B. N. and Shen, Y. (2005). A Bayesian approach to jointly modeling toxicity and biomarker expression in a phase I/II dose-finding trial. Biometrics 61, 343-354.
-
(2005)
Biometrics
, vol.61
, pp. 343-354
-
-
Bekele, B.N.1
Shen, Y.2
-
17
-
-
0003757758
-
Statistical Decision Theory and Bayesian Analysis
-
New York: Springer-Verlag
-
Berger, J. O. (1985). Statistical Decision Theory and Bayesian Analysis. New York: Springer-Verlag.
-
(1985)
-
-
Berger, J.O.1
-
20
-
-
79952079839
-
Adaptive clinical trials: The promise and the caution
-
Berry, D. A. (2011). Adaptive clinical trials: The promise and the caution. Journal of Clinical Oncology 29, 606-609.
-
(2011)
Journal of Clinical Oncology
, vol.29
, pp. 606-609
-
-
Berry, D.A.1
-
21
-
-
0028887994
-
Adaptive assignment versus balanced randomization in clinical trials: A decision analysis
-
Berry, D. A. and Eick, S. G. (1995). Adaptive assignment versus balanced randomization in clinical trials: A decision analysis. Statistics in Medicine 14, 231-246.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 231-246
-
-
Berry, D.A.1
Eick, S.G.2
-
22
-
-
85122716876
-
Bayesian Adaptive Methods for Clinical Trials
-
Chapman & Hall/CRC, Boca Raton
-
Berry, S. M., Carlin, B. P., Lee, J. J., and Müller, P. (2010). Bayesian Adaptive Methods for Clinical Trials. Chapman & Hall/CRC, Boca Raton.
-
(2010)
-
-
Berry, S.M.1
Carlin, B.P.2
Lee, J.J.3
Müller, P.4
-
23
-
-
67649306739
-
Bayesian clinical trials at the University of Texas M
-
Biswas, S., Liu, D. D., Lee, J. J., and Berry, D. A. (2009). Bayesian clinical trials at the University of Texas M. D. Anderson Cancer Center. Clinical Trials 6, 205-216.
-
(2009)
D. Anderson Cancer Center. Clinical Trials
, vol.6
, pp. 205-216
-
-
Biswas, S.1
Liu, D.D.2
Lee, J.J.3
Berry, D.A.4
-
24
-
-
33745250270
-
Optimal adaptive designs in phase III clinical trials for continuous responses with covariates
-
In: Advances in Model-Oriented Design and Analysis-mODa 7, A. D. Bucchianico, H. Läuter, and H. P. Wynn (eds.), Heidelberg: Physica-Verlag
-
Biswas, A. and Mandai, S. (2004). Optimal adaptive designs in phase III clinical trials for continuous responses with covariates. In: Advances in Model-Oriented Design and Analysis-mODa 7, A. D. Bucchianico, H. Läuter, and H. P. Wynn (eds.), pp. 51-59. Heidelberg: Physica-Verlag.
-
(2004)
, pp. 51-59
-
-
Biswas, A.1
Mandai, S.2
-
26
-
-
84946384873
-
The toxicity of poisons applied jointly
-
Bliss, C. I. (1939). The toxicity of poisons applied jointly. Annals of Applied Biology 26, 585-615.
-
(1939)
Annals of Applied Biology
, vol.26
, pp. 585-615
-
-
Bliss, C.I.1
-
27
-
-
0036277621
-
The bivariate continual reassessment method: extending the CRM to phase I trials of two competing outcomes
-
Braun, T. M. (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.M.1
-
28
-
-
33745473565
-
Generalizing the TITE-CRM to adapt for early-and late-onset toxicities
-
Braun, T. M. (2006). Generalizing the TITE-CRM to adapt for early-and late-onset toxicities. Statistics in Medicine 25, 2071-2083.
-
(2006)
Statistics in Medicine
, vol.25
, pp. 2071-2083
-
-
Braun, T.M.1
-
29
-
-
34249289754
-
Simultaneously optimizing dose and schedule of a new cytotoxic agent
-
Braun, T. M., Thall, P. F., Nguyen, H., and de Lima, M. (2007). Simultaneously optimizing dose and schedule of a new cytotoxic agent. Clinical Trials 4, 113-124.
-
(2007)
Clinical Trials
, vol.4
, pp. 113-124
-
-
Braun, T.M.1
Thall, P.F.2
Nguyen, H.3
De Lima, M.4
-
30
-
-
77956823500
-
A hierarchical Bayesian design for phase I trials of novel combinations of cancer therapeutic agents
-
Braun, T. M. and Wang, S. (2010). A hierarchical Bayesian design for phase I trials of novel combinations of cancer therapeutic agents. Biometrics 66, 805-812.
-
(2010)
Biometrics
, vol.66
, pp. 805-812
-
-
Braun, T.M.1
Wang, S.2
-
31
-
-
20744450408
-
Determining a maximum tolerated schedule of a cytotoxic agent
-
Braun, T. M., Yuan, Z., and Thall, P. F. (2005). Determining a maximum tolerated schedule of a cytotoxic agent. Biometrics 61, 335-343.
-
(2005)
Biometrics
, vol.61
, pp. 335-343
-
-
Braun, T.M.1
Yuan, Z.2
Thall, P.F.3
-
33
-
-
0030613470
-
Model selection: An integral part of inference
-
Buckland, S. T., Burnham, K. P., and Augustin, N. H. (1997). Model selection: An integral part of inference. Biometrics 53,603-618.
-
(1997)
Biometrics
, vol.53
, pp. 603-618
-
-
Buckland, S.T.1
Burnham, K.P.2
Augustin, N.H.3
-
34
-
-
59749104832
-
Bayesian Methods for Data Analysis
-
3rded. Boca Raton, FL: Chapman k Hall/CRC
-
Carlin, B. P. and Louis, T. (2008). Bayesian Methods for Data Analysis. 3rded. Boca Raton, FL: Chapman k Hall/CRC.
-
(2008)
-
-
Carlin, B.P.1
Louis, T.2
-
35
-
-
0003594381
-
Statistical Inference
-
2nd ed. Pacific Grove, CA: Duxbury Press
-
Casella, G. and Berger, R. L. (2001). Statistical Inference. 2nd ed. Pacific Grove, CA: Duxbury Press.
-
(2001)
-
-
Casella, G.1
Berger, R.L.2
-
36
-
-
34548822827
-
Adaptive Design Theory and Implementation Using SAS and R
-
Boca Raton, FL: Chapman & Hall/CRC
-
Chang, M. (2008). Adaptive Design Theory and Implementation Using SAS and R. Boca Raton, FL: Chapman & Hall/CRC.
-
(2008)
-
-
Chang, M.1
-
37
-
-
0023522405
-
Designs for group sequential phase II clinical trials
-
Chang, M. N., Therneau, T. M., Wieand, H. S., and Cha, S. S. (1987). Designs for group sequential phase II clinical trials. Biometrics 43, 865-874.
-
(1987)
Biometrics
, vol.43
, pp. 865-874
-
-
Chang, M.N.1
Therneau, T.M.2
Wieand, H.S.3
Cha, S.S.4
-
38
-
-
0003924731
-
Monte Carlo Methods in Bayesian Computation
-
New York: Springer
-
Chen, M., Shao, Q., and Ibrahim, J. G. (2000). Monte Carlo Methods in Bayesian Computation. New York: Springer.
-
(2000)
-
-
Chen, M.1
Shao, Q.2
Ibrahim, J.G.3
-
39
-
-
0347354945
-
An MCMC approach to classical estimation
-
Chernozhukov, V. and Hong, H. (2003). An MCMC approach to classical estimation. Journal of Econometrics 115, 293-346.
-
(2003)
Journal of Econometrics
, vol.115
, pp. 293-346
-
-
Chernozhukov, V.1
Hong, H.2
-
40
-
-
84871180729
-
Dose Finding by the Continual Reassessment Method
-
Boca Raton, FL: Chapman & Hall/CRC
-
Cheung, Y K. (2011). Dose Finding by the Continual Reassessment Method. Boca Raton, FL: Chapman & Hall/CRC.
-
(2011)
-
-
Cheung, Y.K.1
-
41
-
-
0033637096
-
Sequential designs for phase I clinical trials with late-onset toxicities
-
Cheung, Y K. and Chappell, R. (2000). Sequential designs for phase I clinical trials with late-onset toxicities. Biometrics 56, 1177-1182.
-
(2000)
Biometrics
, vol.56
, pp. 1177-1182
-
-
Cheung, Y.K.1
Chappell, R.2
-
42
-
-
84957950832
-
Statistical Methods for Dose-Finding Experiments
-
Chichester, England: John Wiley & Sons
-
Chevret, S. (2006). Statistical Methods for Dose-Finding Experiments. Chichester, England: John Wiley & Sons.
-
(2006)
-
-
Chevret, S.1
-
43
-
-
34548827478
-
Adaptive Design Methods in Clinical Trials
-
Boca Raton, FL: Chapman & Hall/CRC
-
Chow, S.-C. and Chang, M. (2006). Adaptive Design Methods in Clinical Trials. Boca Raton, FL: Chapman & Hall/CRC.
-
(2006)
-
-
Chow, S.-C.1
Chang, M.2
-
44
-
-
21244472033
-
Sample Size Calculations in Clinical Research
-
2nd ed. New York: Marcel Dekker
-
Chow, S.-C, Shao, J., and Chang, M. (2007). Sample Size Calculations in Clinical Research, 2nd ed. New York: Marcel Dekker.
-
(2007)
-
-
Chow, S.-C.1
Shao, J.2
Chang, M.3
-
45
-
-
0017883262
-
A model for association in bivariate life tables and its application in epidemiological studies of familial tendency in chronic disease incidence
-
Clayton, D. G. (1978). A model for association in bivariate life tables and its application in epidemiological studies of familial tendency in chronic disease incidence. Biometrika 65, 141-152.
-
(1978)
Biometrika
, vol.65
, pp. 141-152
-
-
Clayton, D.G.1
-
46
-
-
0000399144
-
Forcing sequential experiments to be balanced
-
Efron, B. (1971). Forcing sequential experiments to be balanced. Biometrika 58, 403-417.
-
(1971)
Biometrika
, vol.58
, pp. 403-417
-
-
Efron, B.1
-
47
-
-
0000552307
-
The two-armed bandit with delayed responses
-
Eick, S. G. (1988). The two-armed bandit with delayed responses. The Annals of Statistics 16, 254-264.
-
(1988)
The Annals of Statistics
, vol.16
, pp. 254-264
-
-
Eick, S.G.1
-
48
-
-
38149145171
-
The doubly adaptive biased coin design for sequential clinical trials
-
Eisele, J. R. (1994). The doubly adaptive biased coin design for sequential clinical trials. Journal of Statistical Planning and Inference 38, 249-262.
-
(1994)
Journal of Statistical Planning and Inference
, vol.38
, pp. 249-262
-
-
Eisele, J.R.1
-
49
-
-
21844519699
-
Central limit theorems for doubly adaptive biased coin designs
-
Eisele, J. R. and Woodroofe, M. (1995). Central limit theorems for doubly adaptive biased coin designs. The Annals of Statistics 23, 234-254.
-
(1995)
The Annals of Statistics
, vol.23
, pp. 234-254
-
-
Eisele, J.R.1
Woodroofe, M.2
-
50
-
-
0021496089
-
Two-stage clinical trial stopping rules
-
Elashoff, J. D. and Reedy, T. J. (1984). Two-stage clinical trial stopping rules. Biometrics 40,791-795.
-
(1984)
Biometrics
, vol.40
, pp. 791-795
-
-
Elashoff, J.D.1
Reedy, T.J.2
-
51
-
-
0033979541
-
Effect of time to complete remission on subsequent survival and disease-free survival time in AML, RAEB-t, and RAEB
-
Estey, E. H., Shen, Y., and Thall, P. F. (2000). Effect of time to complete remission on subsequent survival and disease-free survival time in AML, RAEB-t, and RAEB. Blood 95, 72-77.
-
(2000)
Blood
, vol.95
, pp. 72-77
-
-
Estey, E.H.1
Shen, Y.2
Thall, P.F.3
-
52
-
-
0028060511
-
Practical modification of the continual reassessment methods for phase I cancer clinical trials
-
Faries, D. (1994). Practical modification of the continual reassessment methods for phase I cancer clinical trials. Journal of Biopharmaceutical Statistics 4,147-164.
-
(1994)
Journal of Biopharmaceutical Statistics
, vol.4
, pp. 147-164
-
-
Faries, D.1
-
54
-
-
0032581580
-
Self-designing clinical trials
-
Fisher, L. D. (1998). Self-designing clinical trials. Statistics in Medicine 17, 1551-1562.
-
(1998)
Statistics in Medicine
, vol.17
, pp. 1551-1562
-
-
Fisher, L.D.1
-
55
-
-
85053538802
-
Intention to treat in clinical trials
-
In: Statistical Issues in Drug Research and Development, K. E. Pearce, ed., New York: Marcel Dekker
-
Fisher, L. D., Dixon, D. O., Herson, J., Frankowski, R. K., Hearon, M. S., and Pearce, K. E. (1990). Intention to treat in clinical trials. In: Statistical Issues in Drug Research and Development, K. E. Pearce, ed., pp. 331-350. New York: Marcel Dekker.
-
(1990)
, pp. 331-350
-
-
Fisher, L.D.1
Dixon, D.O.2
Herson, J.3
Frankowski, R.K.4
Hearon, M.S.5
Pearce, K.E.6
-
56
-
-
0020108590
-
One-sample multiple testing procedure for phase II clinical trials
-
Fleming, T. R. (1982). One-sample multiple testing procedure for phase II clinical trials. Biometrics 38, 143-151.
-
(1982)
Biometrics
, vol.38
, pp. 143-151
-
-
Fleming, T.R.1
-
57
-
-
0003855105
-
Counting Processes and Survival Analysis
-
New York: John Wiley & Sons
-
Fleming, T. R. and Harrington, D. (1991). Counting Processes and Survival Analysis. New York: John Wiley & Sons.
-
(1991)
-
-
Fleming, T.R.1
Harrington, D.2
-
58
-
-
74549207384
-
The cross-validated adaptive signature design
-
Freidlin, B., Jiang, W., and Simon, R. (2010). The cross-validated adaptive signature design. Clinical Cancer Research 16, 691-698.
-
(2010)
Clinical Cancer Research
, vol.16
, pp. 691-698
-
-
Freidlin, B.1
Jiang, W.2
Simon, R.3
-
59
-
-
24644438754
-
Evaluation of randomized discontinuation design
-
Freidlin, B. and Simon, R. (2004). Evaluation of randomized discontinuation design. Journal of Clinical Oncology 23, 5094-5098.
-
(2004)
Journal of Clinical Oncology
, vol.23
, pp. 5094-5098
-
-
Freidlin, B.1
Simon, R.2
-
60
-
-
27744537954
-
Adaptive signature design: An adaptive clinical trial design for generating and prospectively testing a gene expression signature for sensitive patients
-
Freidlin, B. and Simon, R. (2005). Adaptive signature design: An adaptive clinical trial design for generating and prospectively testing a gene expression signature for sensitive patients. Clinical Cancer Research 11, 7872-7878.
-
(2005)
Clinical Cancer Research
, vol.11
, pp. 7872-7878
-
-
Freidlin, B.1
Simon, R.2
-
61
-
-
77953469909
-
Fundamentals of Clinical Trials
-
3rd ed. New York: Springer
-
Friedman, L. M., Furberg, C. D., and DeMets, D. L. (1998). Fundamentals of Clinical Trials, 3rd ed. New York: Springer.
-
(1998)
-
-
Friedman, L.M.1
Furberg, C.D.2
DeMets, D.L.3
-
62
-
-
0033918775
-
A curve-free method for phase I clinical trials
-
Gasparini, M. and 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
-
63
-
-
50549174560
-
The determination of the number of patients required in a follow-up trial of a new chemotherapeutic agent
-
Gehan, E. A. (1961). The determination of the number of patients required in a follow-up trial of a new chemotherapeutic agent. Journal of Chronic Diseases 13, 346-353.
-
(1961)
Journal of Chronic Diseases
, vol.13
, pp. 346-353
-
-
Gehan, E.A.1
-
65
-
-
0004012196
-
Bayesian Data Analysis
-
2nd ed. Boca Raton, FL: Chapman & Hall/CRC
-
Gelman, A., Carlin, J. B., Stern, H. S. and Rubin, D. B. (2003). Bayesian Data Analysis, 2nd ed. Boca Raton, FL: Chapman & Hall/CRC.
-
(2003)
-
-
Gelman, A.1
Carlin, J.B.2
Stern, H.S.3
Rubin, D.B.4
-
66
-
-
84972492387
-
Inference from iterative simulation using multiple sequences
-
Gelman, A. and Rubin, D. B. (1992). Inference from iterative simulation using multiple sequences. Statistical Science 7,457-511.
-
(1992)
Statistical Science
, vol.7
, pp. 457-511
-
-
Gelman, A.1
Rubin, D.B.2
-
68
-
-
0001032163
-
Evaluating the accuracy of sampling-based approaches to the calculation of posterior moments
-
In: Bayesian Statistics 4, J. M. Bernardo, J. Berger, A. P. Dawid, and A. F. M. Smith (eds.), Oxford: Oxford University Press
-
Geweke, J. (1992). Evaluating the accuracy of sampling-based approaches to the calculation of posterior moments. In: Bayesian Statistics 4, J. M. Bernardo, J. Berger, A. P. Dawid, and A. F. M. Smith (eds.), pp. 169-193. Oxford: Oxford University Press.
-
(1992)
, pp. 169-193
-
-
Geweke, J.1
-
70
-
-
0038312668
-
Adaptive rejection Metropolis sampling within Gibbs sampling
-
Gilks, W. R" Best, N. G., and Tan, K. K. C. (1995). Adaptive rejection Metropolis sampling within Gibbs sampling. Journal of the Royal Statistical Society, Series C 44,455-472.
-
(1995)
Journal of the Royal Statistical Society, Series C
, vol.44
, pp. 455-472
-
-
Gilks, W.R.1
Best, N.G.2
Tan, K.K.C.3
-
71
-
-
45849117863
-
Importance and challenges of studying marketed drugs: What is a phase IV study? Common clinical research designs, registries, and self-reporting systems
-
Glasser, S. P., Salas, M., and Delzell, E. (2007). Importance and challenges of studying marketed drugs: What is a phase IV study? Common clinical research designs, registries, and self-reporting systems. The Journal of Clinical Pharmacology 47, 1074-1086.
-
(2007)
The Journal of Clinical Pharmacology
, vol.47
, pp. 1074-1086
-
-
Glasser, S.P.1
Salas, M.2
Delzell, E.3
-
72
-
-
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
-
73
-
-
0027949027
-
Simulation as a design tool for phase I/II clinical trial: An example from bone marrow transplantation
-
Gooley, T. A., Martin, P. J., Fisher, L. D., and Pettinger, M. (1994). Simulation as a design tool for phase I/II clinical trial: An example from bone marrow transplantation. Controlled Clinical Trial 15,450-462.
-
(1994)
Controlled Clinical Trial
, vol.15
, pp. 450-462
-
-
Gooley, T.A.1
Martin, P.J.2
Fisher, L.D.3
Pettinger, M.4
-
74
-
-
0026543566
-
Interim analyses for monitoring clinical trials that do not materially affect the type I error rate
-
Gould, A. L. (1992). Interim analyses for monitoring clinical trials that do not materially affect the type I error rate. Statistics in Medicine 11, 55-66.
-
(1992)
Statistics in Medicine
, vol.11
, pp. 55-66
-
-
Gould, A.L.1
-
75
-
-
0035884237
-
Sample size re-estimation: recent developments and practical considerations
-
Gould, A. L. (2001). Sample size re-estimation: recent developments and practical considerations. Statistics in Medicine 20, 2625-2643.
-
(2001)
Statistics in Medicine
, vol.20
, pp. 2625-2643
-
-
Gould, A.L.1
-
76
-
-
0008984727
-
Group sequential methods for clinical trials allowing early acceptance of H0 and incorporating costs
-
Gould, A. L. and Pecore, V. J. (1982). Group sequential methods for clinical trials allowing early acceptance of H0 and incorporating costs. Biometrika 69, 75-80.
-
(1982)
Biometrika
, vol.69
, pp. 75-80
-
-
Gould, A.L.1
Pecore, V.J.2
-
78
-
-
27544460007
-
Generalized Method of Moments
-
New York: Oxford University Press
-
Hall, A. R. (2005). Generalized Method of Moments. New York: Oxford University Press.
-
(2005)
-
-
Hall, A.R.1
-
79
-
-
0000414660
-
Large sample properties of generalized method of moments estimators
-
Hansen, L. P. (1982). Large sample properties of generalized method of moments estimators. Econometrica 50, 1029-1054.
-
(1982)
Econometrica
, vol.50
, pp. 1029-1054
-
-
Hansen, L.P.1
-
80
-
-
0030545862
-
Finite-sample properties of some alternative GMM estimators
-
Hansen, L. P., Heaton, J., and Yaron, A. (1996). Finite-sample properties of some alternative GMM estimators. Journal of Business & Economic Statistics 14, 262-280.
-
(1996)
Journal of Business & Economic Statistics
, vol.14
, pp. 262-280
-
-
Hansen, L.P.1
Heaton, J.2
Yaron, A.3
-
81
-
-
84890913931
-
Maximum likelihood approaches to variance component estimation and to related problems
-
Harville, D. A. (1977). Maximum likelihood approaches to variance component estimation and to related problems. Journal of the American Statistical Association 72, 320-338.
-
(1977)
Journal of the American Statistical Association
, vol.72
, pp. 320-338
-
-
Harville, D.A.1
-
82
-
-
77956890234
-
Monte Carlo sampling methods using Markov chains and their applications
-
Hastings, W. K. (1970). Monte Carlo sampling methods using Markov chains and their applications. Biometrika 57,97-109.
-
(1970)
Biometrika
, vol.57
, pp. 97-109
-
-
Hastings, W.K.1
-
83
-
-
84859431713
-
Basic Pharmacokinetics
-
Boca Raton, FL: CRC Press
-
Hedaya, M. A. (2007). Basic Pharmacokinetics. Boca Raton, FL: CRC Press.
-
(2007)
-
-
Hedaya, M.A.1
-
84
-
-
0033564086
-
Adaptive design improvements in the continual reassessment method for phase I studies
-
Heyd, J. M. and Carlin, B. P. (1999). Adaptive design improvements in the continual reassessment method for phase I studies. Statistics in Medicine 18,1307-1321.
-
(1999)
Statistics in Medicine
, vol.18
, pp. 1307-1321
-
-
Heyd, J.M.1
Carlin, B.P.2
-
85
-
-
0003043542
-
The possible effects of the aggregation of the molecules of haemoglobin on its dissociation curves
-
Hill, A. V. (1910). The possible effects of the aggregation of the molecules of haemoglobin on its dissociation curves. The Journal of Physiology 40, iv-vii.
-
(1910)
The Journal of Physiology
, vol.40
, pp. 4-7
-
-
Hill, A.V.1
-
87
-
-
33645762226
-
A sharper Bonferroni procedure for multiple tests of significance
-
Hochberg, Y. (1988). A sharper Bonferroni procedure for multiple tests of significance. Biometrika 75, 800-802.
-
(1988)
Biometrika
, vol.75
, pp. 800-802
-
-
Hochberg, Y.1
-
88
-
-
0001259111
-
Bayesian model averaging: A tutorial
-
Hoeting, J. A., Madigan, D., Raftery, A. E., and Volinsky, C. T. (1999). Bayesian model averaging: A tutorial. Statistical Science 14, 382-01.
-
(1999)
Statistical Science
, vol.14
, pp. 382-301
-
-
Hoeting, J.A.1
Madigan, D.2
Raftery, A.E.3
Volinsky, C.T.4
-
89
-
-
0003808669
-
Introduction to Mathematical Statistics
-
Upper Saddle River, NJ: Pearson Prentice Hall
-
Hogg, R. V., McKean, J. W., and Craig, A. T. (2005). Introduction to Mathematical Statistics. Upper Saddle River, NJ: Pearson Prentice Hall.
-
(2005)
-
-
Hogg, R.V.1
McKean, J.W.2
Craig, A.T.3
-
90
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm, S. (1979). A simple sequentially rejective multiple test procedure. Scandinavian Journal of Statistics 6, 65-70.
-
(1979)
Scandinavian Journal of Statistics
, vol.6
, pp. 65-70
-
-
Holm, S.1
-
91
-
-
77956889117
-
A class of multivariate failure time distributions
-
Hougaard, P. (1986). A class of multivariate failure time distributions. Biometrika 73, 671-678.
-
(1986)
Biometrika
, vol.73
, pp. 671-678
-
-
Hougaard, P.1
-
92
-
-
0242510866
-
Optimality, variability, power: Evaluating response-adaptive randomization procedures for treatment comparisons
-
Hu, F. and Rosenberger, W. F. (2003). Optimality, variability, power: Evaluating response-adaptive randomization procedures for treatment comparisons. Journal of the American Statistical Association 98, 671-678.
-
(2003)
Journal of the American Statistical Association
, vol.98
, pp. 671-678
-
-
Hu, F.1
Rosenberger, W.F.2
-
93
-
-
84947338325
-
The Theory of Response-Adaptive Randomization in Clinical Trials
-
New York: Wiley
-
Hu, F. and Rosenberger, W. F. (2006). The Theory of Response-Adaptive Randomization in Clinical Trials. New York: Wiley.
-
(2006)
-
-
Hu, F.1
Rosenberger, W.F.2
-
94
-
-
26844516148
-
Asymptotic properties of doubly adaptive biased coin designs for multitreatment clinical trials
-
Hu, F. and Zhang, L. X. (2004). Asymptotic properties of doubly adaptive biased coin designs for multitreatment clinical trials. The Annals of Statistics 32, 268-301.
-
(2004)
The Annals of Statistics
, vol.32
, pp. 268-301
-
-
Hu, F.1
Zhang, L.X.2
-
95
-
-
34547659861
-
A parallel phase MI clinical trial design for combination therapies
-
Huang, X., Biswas, S., Oki, Y, Issa, J. P., and Berry, D. A. (2007). A parallel phase MI clinical trial design for combination therapies. Biometrics 63, 429-436.
-
(2007)
Biometrics
, vol.63
, pp. 429-436
-
-
Huang, X.1
Biswas, S.2
Oki, Y.3
Issa, J.P.4
Berry, D.A.5
-
96
-
-
37549028048
-
Hochberg's step-up method: Cutting corners off Holm's step-down method
-
Huang, Y and Hsu, J. C. (2007). Hochberg's step-up method: Cutting corners off Holm's step-down method. Biometrika 94, 965-975.
-
(2007)
Biometrika
, vol.94
, pp. 965-975
-
-
Huang, Y.1
Hsu, J.C.2
-
97
-
-
21844458704
-
Dose escalation trial designs based on a molecularly targeted endpoint
-
Hunsberger, S., Rubinstein, V. L., Dancey, J., and Korn, E. L. (2005). Dose escalation trial designs based on a molecularly targeted endpoint. Statistics in Medicine 24, 2171-2181.
-
(2005)
Statistics in Medicine
, vol.24
, pp. 2171-2181
-
-
Hunsberger, S.1
Rubinstein, V.L.2
Dancey, J.3
Korn, E.L.4
-
98
-
-
0003917642
-
Bayesian Survival Analysis
-
New York: Springer
-
Ibrahim, J. G., Chen, M., and Sinha, D. (2001). Bayesian Survival Analysis. New York: Springer.
-
(2001)
-
-
Ibrahim, J.G.1
Chen, M.2
Sinha, D.3
-
99
-
-
0036968867
-
Seamlessly expanding a randomized phase II trial to phase III
-
Inoue, L. Y T., Thall, P. F, and Berry, D. A. (2002). Seamlessly expanding a randomized phase II trial to phase III. Biometrics 58, 823-831.
-
(2002)
Biometrics
, vol.58
, pp. 823-831
-
-
Inoue, L.Y.T.1
Thall, P.F.2
Berry, D.A.3
-
100
-
-
0035884462
-
The continual reassessment method and its applications: A Bayesian methodology for phase I cancer clinical trials
-
Ishizuka, N. and Ohashi, Y. (2001). The continual reassessment method and its applications: A Bayesian methodology for phase I cancer clinical trials. Statistics in Medicine 20, 2661-2681.
-
(2001)
Statistics in Medicine
, vol.20
, pp. 2661-2681
-
-
Ishizuka, N.1
Ohashi, Y.2
-
101
-
-
11444260961
-
A play-the-winner type urn model with reduced variability
-
Ivanova, A. (2003). A play-the-winner type urn model with reduced variability. Metrika 58,1-13.
-
(2003)
Metrika
, vol.58
, pp. 1-13
-
-
Ivanova, A.1
-
102
-
-
0003414592
-
Theory of Probability
-
3rd ed. London: Oxford University Press
-
Jeffreys, H. (1961), Theory of Probability, 3rd ed. London: Oxford University Press.
-
(1961)
-
-
Jeffreys, H.1
-
105
-
-
0003831001
-
Group Sequential Methods with Applications to Clinical Trials
-
Boca Raton, FL: Chapman & Hall/CRC
-
Jennison, C. and Tumbull, B. W. (2000). Group Sequential Methods with Applications to Clinical Trials. Boca Raton, FL: Chapman & Hall/CRC.
-
(2000)
-
-
Jennison, C.1
Tumbull, B.W.2
-
106
-
-
70349254459
-
Adaptive randomization for multi-arm comparative clinical trials based on joint efficacy/toxicity outcomes
-
Ji, Y. and Bekele, B. N. (2009). Adaptive randomization for multi-arm comparative clinical trials based on joint efficacy/toxicity outcomes. Biometrics 65, 876-884.
-
(2009)
Biometrics
, vol.65
, pp. 876-884
-
-
Ji, Y.1
Bekele, B.N.2
-
107
-
-
34548619360
-
Dose-finding in phase I clinical trials based on toxicity probability intervals
-
Ji, Y, Li, Y, and Bekele, B. N. (2007). Dose-finding in phase I clinical trials based on toxicity probability intervals. Clinical Trials 4, 235-244.
-
(2007)
Clinical Trials
, vol.4
, pp. 235-244
-
-
Ji, Y.1
Li, Y.2
Bekele, B.N.3
-
108
-
-
34547529131
-
Bayesian dose finding in phase I clinical trials based on a new statistical framework
-
Ji, Y, Li, Y, and Yin, G. (2007). Bayesian dose finding in phase I clinical trials based on a new statistical framework. Statistica Sinica 17, 531-547.
-
(2007)
Statistica Sinica
, vol.17
, pp. 531-547
-
-
Ji, Y.1
Li, Y.2
Yin, G.3
-
109
-
-
34447264769
-
Biomarker-adaptive threshold design: A procedure for evaluating treatment with possible biomarker-defined subset effect
-
Jiang, W., Freidlin, B., and Simon, R. (2007). Biomarker-adaptive threshold design: A procedure for evaluating treatment with possible biomarker-defined subset effect. Journal of National Cancer Institute 99, 1036-1043.
-
(2007)
Journal of National Cancer Institute
, vol.99
, pp. 1036-1043
-
-
Jiang, W.1
Freidlin, B.2
Simon, R.3
-
110
-
-
79956142146
-
Sample Sizes for Clinical Trials
-
Boca Raton, FL: Chapman & Hall/CRC
-
Julious, S. A. (2010). Sample Sizes for Clinical Trials. Boca Raton, FL: Chapman & Hall/CRC.
-
(2010)
-
-
Julious, S.A.1
-
111
-
-
85088938629
-
The Statistical Analysis of Failure Time Data
-
2nd ed. New York: John Wiley
-
Kalbfleisch, J. D. and Prentice, R. L. (2002). The Statistical Analysis of Failure Time Data, 2nd ed. New York: John Wiley.
-
(2002)
-
-
Kalbfleisch, J.D.1
Prentice, R.L.2
-
114
-
-
40049084616
-
Defining, designing, implementing, and evaluating phase 4 HIV prevention effectiveness trials for vulnerable populations
-
Kelly, J. A., Spielberg, F, and McAuliffe, T. L. (2008). Defining, designing, implementing, and evaluating phase 4 HIV prevention effectiveness trials for vulnerable populations. Journal of Acquired Immune Deficiency Syndromes 47, 28-33.
-
(2008)
Journal of Acquired Immune Deficiency Syndromes
, vol.47
, pp. 28-33
-
-
Kelly, J.A.1
Spielberg, F.2
McAuliffe, T.L.3
-
115
-
-
0346307447
-
Limited information likelihood and Bayesian analysis
-
Kim, J.-Y. (2002). Limited information likelihood and Bayesian analysis. Journal of Econometrics 107, 175-193.
-
(2002)
Journal of Econometrics
, vol.107
, pp. 175-193
-
-
Kim, J.-Y.1
-
116
-
-
0027227921
-
Randomized discontinuation trials: Utility and efficiency
-
Kopec, J. A., Abrahamowicz, M., and Esdaile, J. M. (1993). Randomized discontinuation trials: Utility and efficiency. Journal of Clinical Epidemiology 46, 959-971.
-
(1993)
Journal of Clinical Epidemiology
, vol.46
, pp. 959-971
-
-
Kopec, J.A.1
Abrahamowicz, M.2
Esdaile, J.M.3
-
117
-
-
3242721608
-
Nontoxicity endpoints in phase I trial designs for targeted, noncytotoxic agents
-
Kom, E. L. (2004). Nontoxicity endpoints in phase I trial designs for targeted, noncytotoxic agents. Journal of the National Cancer Institute 96, 977-978.
-
(2004)
Journal of the National Cancer Institute
, vol.96
, pp. 977-978
-
-
Kom, E.L.1
-
118
-
-
78650339993
-
Outcome-adaptive randomization: Is it useful?
-
Korn, E. L. and Freidlin, B. (2011) Outcome-adaptive randomization: Is it useful? Journal of Clinical Oncology 29, 771-776.
-
(2011)
Journal of Clinical Oncology
, vol.29
, pp. 771-776
-
-
Korn, E.L.1
Freidlin, B.2
-
119
-
-
0027465147
-
Using the tolerable-dose diagram in the design of Phase I combination chemotherapy trials
-
Korn, E. L. and Simon, R. (1993). Using the tolerable-dose diagram in the design of Phase I combination chemotherapy trials. Journal of Clinical Oncology 11, 794-801.
-
(1993)
Journal of Clinical Oncology
, vol.11
, pp. 794-801
-
-
Korn, E.L.1
Simon, R.2
-
120
-
-
0035154256
-
Clinical trial designs for cytostatic agents: Are new approaches needed?
-
Korn, E. L., Arbuck, S. G., Pluda, J. M., Simon, R., Kaplan, R. S., and Christian, M. C. (2001). Clinical trial designs for cytostatic agents: Are new approaches needed? Journal of Clinical Oncology 19, 265-272.
-
(2001)
Journal of Clinical Oncology
, vol.19
, pp. 265-272
-
-
Korn, E.L.1
Arbuck, S.G.2
Pluda, J.M.3
Simon, R.4
Kaplan, R.S.5
Christian, M.C.6
-
121
-
-
0033618612
-
Continual reassessment methods in phase I trials of the combination of two drugs in oncology
-
Kramar, A., Lebecq, A., and Candalh, E. (1999). Continual reassessment methods in phase I trials of the combination of two drugs in oncology. Statistics in Medicine 18,1849-1864.
-
(1999)
Statistics in Medicine
, vol.18
, pp. 1849-1864
-
-
Kramar, A.1
Lebecq, A.2
Candalh, E.3
-
122
-
-
0001356210
-
A mixture model combining logistic regression with proportional hazards regression
-
Kuk, A. Y. C. and Chen, C. H. (1992). A mixture model combining logistic regression with proportional hazards regression. Biometrika 79, 531-541.
-
(1992)
Biometrika
, vol.79
, pp. 531-541
-
-
Kuk, A.Y.C.1
Chen, C.H.2
-
123
-
-
18244384263
-
Optimal doses of paclitaxel and carboplatin combination chemotherapy for ovarian cancer: A phase I modified continual reassessment method study
-
Kuzuya, K., Ishikawa, H., Nakanishi, T., et al. (2001). Optimal doses of paclitaxel and carboplatin combination chemotherapy for ovarian cancer: A phase I modified continual reassessment method study. International Journal of Clinical Oncology 6,271-278.
-
(2001)
International Journal of Clinical Oncology
, vol.6
, pp. 271-278
-
-
Kuzuya, K.1
Ishikawa, H.2
Nakanishi, T.3
-
124
-
-
0022771685
-
Evaluation of sample size and power for analyses of survival with allowance for nonuniform patient entry, losses to follow-up, noncompliance, and stratification
-
Lachin, J. M. and Foulkes, M. A. (1986). Evaluation of sample size and power for analyses of survival with allowance for nonuniform patient entry, losses to follow-up, noncompliance, and stratification. Biometrics 42, 507-519.
-
(1986)
Biometrics
, vol.42
, pp. 507-519
-
-
Lachin, J.M.1
Foulkes, M.A.2
-
125
-
-
0023896164
-
Sample sizes based on the log-rank statistic in complex clinical trials
-
Lakatos, E. (1988). Sample sizes based on the log-rank statistic in complex clinical trials. Biometrics 44, 229-241.
-
(1988)
Biometrics
, vol.44
, pp. 229-241
-
-
Lakatos, E.1
-
126
-
-
70449529019
-
Discrete sequential boundaries for clinical trials
-
Lan, K. K. G. and DeMets, D. L. (1983). Discrete sequential boundaries for clinical trials. Biometrika 70, 659-663.
-
(1983)
Biometrika
, vol.70
, pp. 659-663
-
-
Lan, K.K.G.1
DeMets, D.L.2
-
127
-
-
78649956851
-
Bayesian adaptive randomization designs for targeted agent development
-
Lee, J. J., Gu, X., and Liu, S. (2010). Bayesian adaptive randomization designs for targeted agent development. 7, 584-596.
-
(2010)
, vol.7
, pp. 584-596
-
-
Lee, J.J.1
Gu, X.2
Liu, S.3
-
128
-
-
34247897031
-
Interaction index and different methods for determining drug interaction in combination therapy
-
Lee, J. J., Kong, M., Ayers, G. D., and Lotan, R. (2007). Interaction index and different methods for determining drug interaction in combination therapy. Journal of Biopharmaceutical Statistics 17,461-180.
-
(2007)
Journal of Biopharmaceutical Statistics
, vol.17
, pp. 461-180
-
-
Lee, J.J.1
Kong, M.2
Ayers, G.D.3
Lotan, R.4
-
129
-
-
43649085358
-
A predictive probability design for phase II cancer
-
Lee, J. J. and Liu, D. D. (2008). A predictive probability design for phase II cancer clinical trials Clinical Trials 5, 93-106.
-
(2008)
clinical trials Clinical Trials
, vol.5
, pp. 93-106
-
-
Lee, J.J.1
Liu, D.D.2
-
130
-
-
0032732411
-
Adaptive sample size calculations in group sequential trials
-
Lehmacher, W. and Wassmer, G. (1999). Adaptive sample size calculations in group sequential trials. Biometrics 55, 1286-1290.
-
(1999)
Biometrics
, vol.55
, pp. 1286-1290
-
-
Lehmacher, W.1
Wassmer, G.2
-
131
-
-
78651428711
-
Bayesian phase II clinical trial design with time-to-event adaptive randomization
-
Lei, X., Yuan, Y, and Yin, G. (2011). Bayesian phase II clinical trial design with time-to-event adaptive randomization. Lifetime Data Analysis 17, 156-174.
-
(2011)
Lifetime Data Analysis
, vol.17
, pp. 156-174
-
-
Lei, X.1
Yuan, Y.2
Yin, G.3
-
132
-
-
0037080851
-
An extension of the continual reassessment method using decision theory
-
Leung, D. H.-Y and Wang, Y.-G. (2002). An extension of the continual reassessment method using decision theory. Statistics in Medicine 21, 51-63.
-
(2002)
Statistics in Medicine
, vol.21
, pp. 51-63
-
-
Leung, D.H.-Y.1
Wang, Y.-G.2
-
133
-
-
59849118019
-
Dose-schedule finding in phase I/II clinical trials using a Bayesian isotonic transformation
-
Li, Y, Bekele, B. N., Ji, Y, and Cook, J. D. (2008). Dose-schedule finding in phase I/II clinical trials using a Bayesian isotonic transformation. Statistics in Medicine 27,4895-4913.
-
(2008)
Statistics in Medicine
, vol.27
, pp. 4895-4913
-
-
Li, Y.1
Bekele, B.N.2
Ji, Y.3
Cook, J.D.4
-
134
-
-
77649173768
-
Longitudinal data analysis using generalized linear models
-
Liang, K. Y and Zeger, S. L. (1986). Longitudinal data analysis using generalized linear models. Biometrika 73,13-22.
-
(1986)
Biometrika
, vol.73
, pp. 13-22
-
-
Liang, K.Y.1
Zeger, S.L.2
-
135
-
-
0012957270
-
Statistical properties of the traditional algorithm-based designs for phase I cancer clinical trials
-
Lin, Y. and Shih, W. J. (2001). Statistical properties of the traditional algorithm-based designs for phase I cancer clinical trials. Biostatistics 2, 203-215.
-
(2001)
Biostatistics
, vol.2
, pp. 203-215
-
-
Lin, Y.1
Shih, W.J.2
-
136
-
-
0003535322
-
A Treatise of the Scurvy
-
Edinburgh: Sands, Murray, Cochran. Reprinted in Lind's Treatise on Scurvy, C. P. Stewart and D. Guthrie, eds. Edinburgh: Edinburgh University Press
-
Lind, J. (1753). A Treatise of the Scurvy. Edinburgh: Sands, Murray, Cochran. Reprinted in Lind's Treatise on Scurvy, C. P. Stewart and D. Guthrie, eds. Edinburgh: Edinburgh University Press.
-
(1753)
-
-
Lind, J.1
-
137
-
-
0007221106
-
Inference for a Bernoulli process (a Bayesian view)
-
Lindley, D. V. and Phillips, L. D. (1976). Inference for a Bernoulli process (a Bayesian view). American Statistician 30, 112-119.
-
(1976)
American Statistician
, vol.30
, pp. 112-119
-
-
Lindley, D.V.1
Phillips, L.D.2
-
138
-
-
85101444608
-
Statistical Analysis with Missing Data
-
2nd ed. New York: Wiley
-
Little, R. J. A. and Rubin, D. B. (2002). Statistical Analysis with Missing Data, 2nd ed. New York: Wiley.
-
(2002)
-
-
Little, R.J.A.1
Rubin, D.B.2
-
139
-
-
0037198998
-
Sample size and power determination for clustered repeated measurements
-
Liu, A., Shih, W. J., and Gehan, E. A. (2002). Sample size and power determination for clustered repeated measurements. Statistics in Medicine 21, 1787-1801.
-
(2002)
Statistics in Medicine
, vol.21
, pp. 1787-1801
-
-
Liu, A.1
Shih, W.J.2
Gehan, E.A.3
-
140
-
-
0030799449
-
Sample size calculations for studies with correlated observations
-
Liu, G. and Liang, K. Y. (1997). Sample size calculations for studies with correlated observations. Biometrics 53, 937-947.
-
(1997)
Biometrics
, vol.53
, pp. 937-947
-
-
Liu, G.1
Liang, K.Y.2
-
141
-
-
0035106146
-
On sample size and inference for two-stage adaptive designs
-
Liu, Q. and Chi, G. Y. H. (2001). On sample size and inference for two-stage adaptive designs. Biometrics 57, 172-177.
-
(2001)
Biometrics
, vol.57
, pp. 172-177
-
-
Liu, Q.1
Chi, G.Y.H.2
-
143
-
-
0001663843
-
The problem of synergism and antagonism of combined drugs
-
Loewe, S. (1953). The problem of synergism and antagonism of combined drugs. Arzeim Forsch 3, 285-290.
-
(1953)
Arzeim Forsch
, vol.3
, pp. 285-290
-
-
Loewe, S.1
-
144
-
-
0034908645
-
Phase I clinical trial of weekly combined topotecan and irinotecan
-
Lokich, J. (2001). Phase I clinical trial of weekly combined topotecan and irinotecan. American Journal Clinical Oncology 24, 336-340.
-
(2001)
American Journal Clinical Oncology
, vol.24
, pp. 336-340
-
-
Lokich, J.1
-
145
-
-
0017694437
-
Sequential allocation in clinical trials comparing two exponential survival curves
-
Louis, T. A. (1977). Sequential allocation in clinical trials comparing two exponential survival curves. Biometrics 33, 627-634.
-
(1977)
Biometrics
, vol.33
, pp. 627-634
-
-
Louis, T.A.1
-
146
-
-
84950945692
-
Model selection and accounting for model uncertainty in graphical models using Occam's window
-
Madigan, D. and Raftery, A. E. (1994). Model selection and accounting for model uncertainty in graphical models using Occam's window. Journal of the American Statistical Association 89, 1535-1546.
-
(1994)
Journal of the American Statistical Association
, vol.89
, pp. 1535-1546
-
-
Madigan, D.1
Raftery, A.E.2
-
147
-
-
0003776533
-
Survival Analysis with Long-Term Survivors
-
New York: Wiley
-
Mailer, R. A. and Zhou, X. (1996). Survival Analysis with Long-Term Survivors. New York: Wiley.
-
(1996)
-
-
Mailer, R.A.1
Zhou, X.2
-
148
-
-
69849108427
-
Clinical trial designs for predictive biomarker validation: Theoretical considerations and practical challenges
-
Mandrekar, S. J. and Sargent, D. J. (2009). Clinical trial designs for predictive biomarker validation: Theoretical considerations and practical challenges. Journal of Clinical Oncology 27, 4027-4034.
-
(2009)
Journal of Clinical Oncology
, vol.27
, pp. 4027-4034
-
-
Mandrekar, S.J.1
Sargent, D.J.2
-
149
-
-
0017146303
-
On closed testing procedures with special reference to ordered analysis of variance
-
Marcus, R., Peritz, E., and Gabriel, K. R. (1976). On closed testing procedures with special reference to ordered analysis of variance. Biometrika 63, 655-660.
-
(1976)
Biometrika
, vol.63
, pp. 655-660
-
-
Marcus, R.1
Peritz, E.2
Gabriel, K.R.3
-
150
-
-
79956107922
-
Dose-finding approach for dose escalation with overdose control considering incomplete observations
-
Mauguen, A., Le Deleya, M. C, and Zohar, S. (2011). Dose-finding approach for dose escalation with overdose control considering incomplete observations. Statistics in Medicine 20, 1584-1594.
-
(2011)
Statistics in Medicine
, vol.20
, pp. 1584-1594
-
-
Mauguen, A.1
Le Deleya, M.2
Zohar, S.3
-
152
-
-
0003663926
-
Generalized Linear Models
-
2nd ed. London: Chapman & Hall
-
McCullagh, P. and Neider, J. A. (1989). Generalized Linear Models, 2nd ed. London: Chapman & Hall.
-
(1989)
-
-
McCullagh, P.1
Neider, J.A.2
-
153
-
-
77951529251
-
Streptomycin treatment of pulmonary tuberculosis
-
Medical Research Council
-
Medical Research Council. (1948). Streptomycin treatment of pulmonary tuberculosis. British Medical Journal 2, 769-782.
-
(1948)
British Medical Journal
, vol.2
, pp. 769-782
-
-
-
154
-
-
0035628922
-
An adaptive randomized design with application to estimation
-
Melfi, V., Page, C, and Geraldes, M. (2001). An adaptive randomized design with application to estimation. Canadian Journal of Statistics 29,107-116.
-
(2001)
Canadian Journal of Statistics
, vol.29
, pp. 107-116
-
-
Melfi, V.1
Page, C.2
Geraldes, M.3
-
155
-
-
5744249209
-
Equations of state calculations by fast computing machines
-
Metropolis, N., Rosenbluth, A. W., Rosenbluth, M. N., Teller, A. H., and Teller, E. (1953). Equations of state calculations by fast computing machines. Journal of Chemical Physics 21, 1087-1092.
-
(1953)
Journal of Chemical Physics
, vol.21
, pp. 1087-1092
-
-
Metropolis, N.1
Rosenbluth, A.W.2
Rosenbluth, M.N.3
Teller, A.H.4
Teller, E.5
-
156
-
-
69949162760
-
Gefitinib or carboplatinpaclitaxel in pulmonary adenocarcinoma
-
Mok, T. S., Wu, Y.-L., Thongprasert, S., et al. (2009). Gefitinib or carboplatinpaclitaxel in pulmonary adenocarcinoma. The New England Journal of Medicine 361,947-957.
-
(2009)
The New England Journal of Medicine
, vol.361
, pp. 947-957
-
-
Mok, T.S.1
Wu, Y.-L.2
Thongprasert, S.3
-
157
-
-
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
-
M0ller, 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
-
158
-
-
0003448104
-
Analysis of Quantal Response Data
-
London: Chapman h Hall
-
Morgan, B. J. T. (1992). Analysis of Quantal Response Data. London: Chapman h Hall.
-
(1992)
-
-
Morgan, B.J.T.1
-
159
-
-
2442461297
-
Multiple Analyses in Clinical Trials: Fundamentals for Investigators
-
New York: Springer-Verlag
-
Moyé, L. A. (2003) Multiple Analyses in Clinical Trials: Fundamentals for Investigators. New York: Springer-Verlag.
-
(2003)
-
-
Moyé, L.A.1
-
160
-
-
1342289781
-
Phase I trial using a time-to-event continual reassessment strategy for dose escalation of cisplatin combined with gemcitabine and radiation therapy in pancreatic cancer
-
Muler, J. H., McGinn, C. J., Normolle, D. Lawrence, T., Brown, D., Hejna, G., and Zalupski, M. M. (2004). Phase I trial using a time-to-event continual reassessment strategy for dose escalation of cisplatin combined with gemcitabine and radiation therapy in pancreatic cancer. Journal of Clinical Oncology 22,238-243.
-
(2004)
Journal of Clinical Oncology
, vol.22
, pp. 238-243
-
-
Muler, J.H.1
McGinn, C.J.2
Normolle, D.3
Lawrence, T.4
Brown, D.5
Hejna, G.6
Zalupski, M.M.7
-
161
-
-
0034876356
-
Adaptive group sequential designs for clinical trials: Combining the advantages of adaptive and of classical group sequential approaches
-
Müller, H.-H. and Schäfer, H. (2001). Adaptive group sequential designs for clinical trials: Combining the advantages of adaptive and of classical group sequential approaches. Biometrics 57, 886-891.
-
(2001)
Biometrics
, vol.57
, pp. 886-891
-
-
Müller, H.-H.1
Schäfer, H.2
-
163
-
-
0004156740
-
An Introduction to Copulas
-
New York: Springer-Verlag
-
Nelsen, R. B. (1999). An Introduction to Copulas. New York: Springer-Verlag.
-
(1999)
-
-
Nelsen, R.B.1
-
164
-
-
77955142569
-
Response-adaptive randomization for clinical trials with adjustment for covariate imbalance
-
Ning, J. and Huang, X. (2010). Response-adaptive randomization for clinical trials with adjustment for covariate imbalance. Statistics in Medicine 29,1761-1768.
-
(2010)
Statistics in Medicine
, vol.29
, pp. 1761-1768
-
-
Ning, J.1
Huang, X.2
-
165
-
-
0018687930
-
A multiple testing procedure for clinical trials
-
O'Brien, P. C. and Fleming, T. R. (1979). A multiple testing procedure for clinical trials. Biometrics 35, 549-556.
-
(1979)
Biometrics
, vol.35
, pp. 549-556
-
-
O'Brien, P.C.1
Fleming, T.R.2
-
166
-
-
0025986460
-
Methods for dose finding studies in cancer clinical trials: A review and results of a Monte Carlo study
-
O'Quigley, J. and Chevret, S. (1991). Methods for dose finding studies in cancer clinical trials: A review and results of a Monte Carlo study. Statistics in Medicine 10,1647-1664.
-
(1991)
Statistics in Medicine
, vol.10
, pp. 1647-1664
-
-
O'Quigley, J.1
Chevret, S.2
-
167
-
-
0035186085
-
Dose-finding designs for HIV studies
-
O'Quigley, J., Hughes, M. D., and 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.D.2
Fenton, T.3
-
168
-
-
0037869516
-
Continual reassessment method for ordered groups
-
O'Quigley, J. and Paoletti, X. (2003). Continual reassessment method for ordered groups. Biometrics 59,430-440.
-
(2003)
Biometrics
, vol.59
, pp. 430-440
-
-
O'Quigley, J.1
Paoletti, X.2
-
169
-
-
0025148278
-
Continual reassessment method: A practical design for Phase I clinical trials in cancer
-
O'Quigley, J., Pepe, M., and Fisher, L. D. (1990). Continual reassessment method: A practical design for Phase I clinical trials in cancer. Biometrics 46, 33-8.
-
(1990)
Biometrics
, vol.46
, pp. 33-38
-
-
O'Quigley, J.1
Pepe, M.2
Fisher, L.D.3
-
170
-
-
0029938415
-
Continual reassessment method: A likelihood approach
-
O'Quigley, J. and 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
-
171
-
-
0003576016
-
Clinical Trials: A Methodologie Perspective
-
2nd ed. New York: John Wiley & Sons
-
Piantadosi, S. (2005). Clinical Trials: A Methodologie Perspective. 2nd ed. New York: John Wiley & Sons.
-
(2005)
-
-
Piantadosi, S.1
-
172
-
-
0031888716
-
Practical implementation of a modified continual reassessment method for dose finding trials
-
Piantadosi, S., Fisher, J., and Grossman, S. (1998). Practical implementation of a modified continual reassessment method for dose finding trials. Cancer Chemotherapy and Pharmacology 41, 429-436.
-
(1998)
Cancer Chemotherapy and Pharmacology
, vol.41
, pp. 429-436
-
-
Piantadosi, S.1
Fisher, J.2
Grossman, S.3
-
173
-
-
0014067610
-
A comparison of two approaches to the construction of models for quantal responses to mixtures of drugs
-
Plackett, R. L. and Hewlett, P. S. (1967). A comparison of two approaches to the construction of models for quantal responses to mixtures of drugs. Biometrics 23, 27-44.
-
(1967)
Biometrics
, vol.23
, pp. 27-44
-
-
Plackett, R.L.1
Hewlett, P.S.2
-
174
-
-
0017744944
-
Group sequential methods in the design and analysis of clinical trials
-
Pocock, S. J. (1977). Group sequential methods in the design and analysis of clinical trials. Biometrika 64, 191-199.
-
(1977)
Biometrika
, vol.64
, pp. 191-199
-
-
Pocock, S.J.1
-
175
-
-
0016799829
-
Sequential treatment assignment with balancing for prognostic factors in the controlled clinical trials
-
Pocock, S. J. and Simon, R. (1975). Sequential treatment assignment with balancing for prognostic factors in the controlled clinical trials. Biometrics 31, 103-115.
-
(1975)
Biometrics
, vol.31
, pp. 103-115
-
-
Pocock, S.J.1
Simon, R.2
-
177
-
-
0033637709
-
Interim analysis and sample size reassessment
-
Posch, M. and Bauer, P. (2000). Interim analysis and sample size reassessment. Biometrics 56,1170-1176.
-
(2000)
Biometrics
, vol.56
, pp. 1170-1176
-
-
Posch, M.1
Bauer, P.2
-
178
-
-
0029589385
-
Designed extension of studies based on conditional power
-
Proschan, M. A. and Hunsberger, S. A. (1995). Designed extension of studies based on conditional power. Biometrics 51, 1315-1324.
-
(1995)
Biometrics
, vol.51
, pp. 1315-1324
-
-
Proschan, M.A.1
Hunsberger, S.A.2
-
179
-
-
0031506560
-
Bayesian model averaging for linear regression models
-
Raftery, A. E., Madigan, D., and Hoeting, J. A. (1997). Bayesian model averaging for linear regression models. Journal of the American Statistical Association 92, 179-191.
-
(1997)
Journal of the American Statistical Association
, vol.92
, pp. 179-191
-
-
Raftery, A.E.1
Madigan, D.2
Hoeting, J.A.3
-
180
-
-
57849154374
-
Optimising the design of phase II oncology trials: the importance of randomisation
-
Ratain, M. J. and Sargent, D. J. (2009). Optimising the design of phase II oncology trials: the importance of randomisation. European Journal of Cancer 45, 275-280.
-
(2009)
European Journal of Cancer
, vol.45
, pp. 275-280
-
-
Ratain, M.J.1
Sargent, D.J.2
-
181
-
-
84966203785
-
Some aspects of the sequential design of experiments
-
Robbins, H. (1952). Some aspects of the sequential design of experiments. Bulletin of the American Mathematical Society 58, 527-535.
-
(1952)
Bulletin of the American Mathematical Society
, vol.58
, pp. 527-535
-
-
Robbins, H.1
-
182
-
-
0026354285
-
Sample size calculations for two-group repeated-measures experiments
-
Rochon, J. (1991). Sample size calculations for two-group repeated-measures experiments. Biometrics 47, 1383-1398.
-
(1991)
Biometrics
, vol.47
, pp. 1383-1398
-
-
Rochon, J.1
-
183
-
-
0000364767
-
New directions in adaptive designs
-
Rosenberger, W. F. (1996). New directions in adaptive designs. Statistical Science 11, 137-149.
-
(1996)
Statistical Science
, vol.11
, pp. 137-149
-
-
Rosenberger, W.F.1
-
184
-
-
0004228040
-
Randomization in Clinical Trials: Theory and Practice
-
New York: John Wiley & Sons
-
Rosenberger, W. F. andLachin, J. M. (2002). Randomization in Clinical Trials: Theory and Practice. New York: John Wiley & Sons.
-
(2002)
-
-
Rosenberger, W.F.1
Lachin, J.M.2
-
185
-
-
0034862727
-
Optimal adaptive designs for binary response trials
-
Rosenberger, W. F., Stallard, N., Ivanova, A., Harper, C, and Ricks, M. (2001). Optimal adaptive designs for binary response trials. Biometrics 57, 909-913.
-
(2001)
Biometrics
, vol.57
, pp. 909-913
-
-
Rosenberger, W.F.1
Stallard, N.2
Ivanova, A.3
Harper, C.4
Ricks, M.5
-
186
-
-
0037112181
-
Randomized discontinuation design: Application to cytostatic antineoplastic agents
-
Rosner, G. L., Stadler, W., and Ratain, M. J. (2002). Randomized discontinuation design: Application to cytostatic antineoplastic agents. Journal of Clinical Oncology 20, 4478-4484.
-
(2002)
Journal of Clinical Oncology
, vol.20
, pp. 4478-4484
-
-
Rosner, G.L.1
Stadler, W.2
Ratain, M.J.3
-
187
-
-
67651220673
-
Reasons for response differences seen in the V15-32, INTEREST and IRASS trials
-
Saijo, N., Takeuchi, M., and Kunitoh, H. (2009). Reasons for response differences seen in the V15-32, INTEREST and IRASS trials. Nature Reviews Clinical Oncology 6, 287-294.
-
(2009)
Nature Reviews Clinical Oncology
, vol.6
, pp. 287-294
-
-
Saijo, N.1
Takeuchi, M.2
Kunitoh, H.3
-
188
-
-
15744374441
-
Clinical trial designs for predictive marker validation in cancer treatment trials
-
Sargent, D. J., Conley, B. A., Allegra, C, and Collette, L. (2005). Clinical trial designs for predictive marker validation in cancer treatment trials. Journal of Clinical Oncology 23, 2020-2027.
-
(2005)
Journal of Clinical Oncology
, vol.23
, pp. 2020-2027
-
-
Sargent, D.J.1
Conley, B.A.2
Allegra, C.3
Collette, L.4
-
189
-
-
0032352436
-
Some probability inequalities for ordered MTP2 random variables: A proof of the Simes conjecture
-
Sarkar, S. (1998). Some probability inequalities for ordered MTP2 random variables: A proof of the Simes conjecture. The Annals of Statistics 26,494-504.
-
(1998)
The Annals of Statistics
, vol.26
, pp. 494-504
-
-
Sarkar, S.1
-
190
-
-
0031312687
-
Semiparametric efficiency and its implication on the design and analysis of group sequential studies
-
Scharfstein, D. O., Tsiatis, A. A., and Robins, J. M. (1997). Semiparametric efficiency and its implication on the design and analysis of group sequential studies. Journal of the American Statistical Association 92, 1342-1350.
-
(1997)
Journal of the American Statistical Association
, vol.92
, pp. 1342-1350
-
-
Scharfstein, D.O.1
Tsiatis, A.A.2
Robins, J.M.3
-
191
-
-
0000549737
-
The asymptotic properties of nonparametric tests for comparing survival distributions
-
Schoenfeld, D. (1981). The asymptotic properties of nonparametric tests for comparing survival distributions. Biometrika 68, 316-319.
-
(1981)
Biometrika
, vol.68
, pp. 316-319
-
-
Schoenfeld, D.1
-
192
-
-
0023887940
-
Power/sample size calculations for generalized linear models
-
Self, S. G. and Mauritsen, R. H. (1988). Power/sample size calculations for generalized linear models. Biometrics 44,79-86.
-
(1988)
Biometrics
, vol.44
, pp. 79-86
-
-
Self, S.G.1
Mauritsen, R.H.2
-
193
-
-
0003708953
-
Large Sample Methods in Statistics
-
New York: Chapman & Hall
-
Sen, P. K. and Singer, J. M. (1993). Large Sample Methods in Statistics. New York: Chapman & Hall.
-
(1993)
-
-
Sen, P.K.1
Singer, J.M.2
-
194
-
-
0033802639
-
Clinical and pharmacological phase I study with accelerated titration design of a daily times five schedule of BBR3464, a novel cationic triplatinum complex
-
Sessa, C. Capri, G., Gianni, L., Peccatori, F., Grasselli, G., Bauer, J., Zucchetti, M., Vigano, L., Gatti, A., Minoia, C, Liati, P., Van den Bosch, S., Bernareggi, A. and Camboni, G., and Marsoni, S. (2000). Clinical and pharmacological phase I study with accelerated titration design of a daily times five schedule of BBR3464, a novel cationic triplatinum complex. Annals of Oncology 11, 977-983.
-
(2000)
Annals of Oncology
, vol.11
, pp. 977-983
-
-
Sessa, C.1
Capri, G.2
Gianni, L.3
Peccatori, F.4
Grasselli, G.5
Bauer, J.6
Zucchetti, M.7
Vigano, L.8
Gatti, A.9
Minoia, C.10
Liati, P.11
Van Den Bosch, S.12
Bernareggi, A.13
Camboni, G.14
Marsoni, S.15
-
195
-
-
77952827491
-
A theory for testing hypotheses under covariate-adaptive randomization
-
Shao, J., Yu, X., and Zhong, B. (2010). A theory for testing hypotheses under covariate-adaptive randomization. Biometrika 97, 347-360.
-
(2010)
Biometrika
, vol.97
, pp. 347-360
-
-
Shao, J.1
Yu, X.2
Zhong, B.3
-
196
-
-
33746402001
-
Consistency of continual reassessment method under model misspecification
-
Shen, L. Z. and O'Quigley, J. (1996). Consistency of continual reassessment method under model misspecification. Biometrika 83, 395-405.
-
(1996)
Biometrika
, vol.83
, pp. 395-405
-
-
Shen, L.Z.1
O'Quigley, J.2
-
197
-
-
85046518420
-
Statistical inference for self-designing clinical trials with a one-sided hypothesis
-
Shen, L. Z. and O'Quigley, J. (1996). Statistical inference for self-designing clinical trials with a one-sided hypothesis. Biometrics 55, 190-197.
-
(1996)
Biometrics
, vol.55
, pp. 190-197
-
-
Shen, L.Z.1
O'Quigley, J.2
-
198
-
-
0002906096
-
Sample size reestimation in clinical trials
-
In: Biopharmaceutical Sequential Statistical Applications, New York: Marcel Dekker
-
Shih, W. J. (1992). Sample size reestimation in clinical trials. In: Biopharmaceutical Sequential Statistical Applications, pp. 285-301. New York: Marcel Dekker.
-
(1992)
, pp. 285-301
-
-
Shih, W.J.1
-
199
-
-
0035961473
-
Sample size re-estimation-journey for a decade
-
Shih, W. J. (2001). Sample size re-estimation-journey for a decade. Statistics in Medicine 20, 515-518.
-
(2001)
Statistics in Medicine
, vol.20
, pp. 515-518
-
-
Shih, W.J.1
-
200
-
-
0035961515
-
Type I error in sample size re-estimations based on observed treatment difference
-
Shun, Z., Yuan, W., Brady, W., and Hsu, H. (2001). Type I error in sample size re-estimations based on observed treatment difference. Statistics in Medicine 20, 497-513.
-
(2001)
Statistics in Medicine
, vol.20
, pp. 497-513
-
-
Shun, Z.1
Yuan, W.2
Brady, W.3
Hsu, H.4
-
201
-
-
0018750994
-
Restricted randomization in clinical trials
-
Simon, R. (1979). Restricted randomization in clinical trials. Biometrics 35,503-512.
-
(1979)
Biometrics
, vol.35
, pp. 503-512
-
-
Simon, R.1
-
202
-
-
0024536437
-
Optimal two-stage designs for phase II clinical trials
-
Simon, R. (1989). Optimal two-stage designs for phase II clinical trials. Controlled Clinical Trials 10, 1-10.
-
(1989)
Controlled Clinical Trials
, vol.10
, pp. 1-10
-
-
Simon, R.1
-
203
-
-
79952271992
-
Advances in clinical trial designs for predictive biomarker discovery and validation
-
Simon, R. (2009). Advances in clinical trial designs for predictive biomarker discovery and validation. Current Breast Cancer Reports 1, 216-221.
-
(2009)
Current Breast Cancer Reports
, vol.1
, pp. 216-221
-
-
Simon, R.1
-
204
-
-
0030749549
-
Accelerated titration designs for phase I clinical trials in oncology
-
Simon, R., Freidlin, B., Rubinstein, L. V., Arbuck, S., Collins, J., and 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.V.3
Arbuck, S.4
Collins, J.5
Christian, M.6
-
205
-
-
0024452804
-
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
-
206
-
-
0012863523
-
Bayesian Approaches to Clinical Trials and Health-Care Evaluation
-
England: John Wiley & Sons
-
Spiegelhalter, D. J., Abrams, K. R., and Myles, J. P. (2004). Bayesian Approaches to Clinical Trials and Health-Care Evaluation. England: John Wiley & Sons.
-
(2004)
-
-
Spiegelhalter, D.J.1
Abrams, K.R.2
Myles, J.P.3
-
207
-
-
0036435040
-
Bayesian measures of model complexity and fit
-
Spiegelhalter, D. J., Best, N. G., Carlin, B. P., and van der Linde, A. (2002). Bayesian measures of model complexity and fit. Journal of the Royal Statistical Society, Series 5 64,583-616.
-
(2002)
Journal of the Royal Statistical Society, Series 5
, vol.64
, pp. 583-616
-
-
Spiegelhalter, D.J.1
Best, N.G.2
Carlin, B.P.3
Van Der Linde, A.4
-
208
-
-
33646183685
-
How the US drag safety system should be changed
-
Strom, B. L. (2006). How the US drag safety system should be changed. Journal of American Medical Association 295,2072-2074.
-
(2006)
Journal of American Medical Association
, vol.295
, pp. 2072-2074
-
-
Strom, B.L.1
-
209
-
-
0036191646
-
Dose finding using the biased coin up-anddown design and isotonic regression
-
Stylianou, M. and Flournoy, N. (2002). Dose finding using the biased coin up-anddown design and isotonic regression. Biometrics 58, 171-177.
-
(2002)
Biometrics
, vol.58
, pp. 171-177
-
-
Stylianou, M.1
Flournoy, N.2
-
210
-
-
33947186623
-
The Statistical Analysis of Interval-Censored Failure Time Data
-
New York: Springer
-
Sun, J. (2006). The Statistical Analysis of Interval-Censored Failure Time Data. New York: Springer.
-
(2006)
-
-
Sun, J.1
-
211
-
-
0038726249
-
Experimental design and sample size determination for testing synergism in drug combination studies based on uniform measures
-
Tan, M., Fang, H., Tian, G., and Houghton, P. J. (2003). Experimental design and sample size determination for testing synergism in drug combination studies based on uniform measures. Statistics in Medicine 22, 2091-2100.
-
(2003)
Statistics in Medicine
, vol.22
, pp. 2091-2100
-
-
Tan, M.1
Fang, H.2
Tian, G.3
Houghton, P.J.4
-
212
-
-
84950758368
-
The calculation of posterior distributions by data augmentation (with discussion)
-
Tanner, M. A. and Wong, W. H. (1987). The calculation of posterior distributions by data augmentation (with discussion). Journal of the American Statistical Association 82, 528-550.
-
(1987)
Journal of the American Statistical Association
, vol.82
, pp. 528-550
-
-
Tanner, M.A.1
Wong, W.H.2
-
213
-
-
0016211783
-
Minimization: A new method of assigning patients to treatment and control groups
-
Taves, D. R. (1974). Minimization: A new method of assigning patients to treatment and control groups. Clinical Pharmacology and Therapeutics 15,443-453.
-
(1974)
Clinical Pharmacology and Therapeutics
, vol.15
, pp. 443-453
-
-
Taves, D.R.1
-
214
-
-
0029129572
-
Semi-parametric estimation in failure time mixture models
-
Taylor, J. M. G. (1995). Semi-parametric estimation in failure time mixture models. Biometrics 51, 899-907.
-
(1995)
Biometrics
, vol.51
, pp. 899-907
-
-
Taylor, J.M.G.1
-
215
-
-
4444272419
-
Dose-finding based on toxicity-efficacy trade-offs
-
Thall, P. F. and Cook, J. (2004). Dose-finding based on toxicity-efficacy trade-offs. Biometrics 60, 684-693.
-
(2004)
Biometrics
, vol.60
, pp. 684-693
-
-
Thall, P.F.1
Cook, J.2
-
216
-
-
0041833622
-
Dose-finding with two agents in phase I oncology trials
-
Thall, P. F, Millikan, R. E., Müller, P., and Lee, S.-J. (2003). Dose-finding with two agents in phase I oncology trials. Biometrics 59, 487-496.
-
(2003)
Biometrics
, vol.59
, pp. 487-496
-
-
Thall, P.F.1
Millikan, R.E.2
Müller, P.3
Lee, S.-J.4
-
217
-
-
0031953966
-
A strategy for dose-finding and safety monitoring based on efficacy and adverse outcomes in phase I/II clinical trials
-
Thall, P. F. and Russell, K. E. (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.F.1
Russell, K.E.2
-
218
-
-
0028279806
-
Practical Bayesian guidelines for phase IIB clinical trials
-
Thall, P. F. and Simon, R. (1994). Practical Bayesian guidelines for phase IIB clinical trials. Biometrics 50, 337-349.
-
(1994)
Biometrics
, vol.50
, pp. 337-349
-
-
Thall, P.F.1
Simon, R.2
-
219
-
-
0028900407
-
Bayesian sequential monitoring designs for single-arm clinical trials with multiple outcomes
-
Thall, P. F, Simon, R., and Estey, E. H. (1995). Bayesian sequential monitoring designs for single-arm clinical trials with multiple outcomes. Statistics in Medicine 14, 357-379.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 357-379
-
-
Thall, P.F.1
Simon, R.2
Estey, E.H.3
-
220
-
-
33847666453
-
Practical Bayesian adaptive randomisation in clinical trials
-
Thall, P. F and Wathen, K. J. (2007). Practical Bayesian adaptive randomisation in clinical trials. European Journal of Cancer 43, 859-866.
-
(2007)
European Journal of Cancer
, vol.43
, pp. 859-866
-
-
Thall, P.F.1
Wathen, K.J.2
-
221
-
-
0001395850
-
On the likelihood that one unknown probability exceeds another in the revises of the evidence of the two samples
-
Thompson, W. R. (1933). On the likelihood that one unknown probability exceeds another in the revises of the evidence of the two samples. Biometrika 25,275-294.
-
(1933)
Biometrika
, vol.25
, pp. 275-294
-
-
Thompson, W.R.1
-
222
-
-
0027538570
-
How many stratification factors are "too many" to use in a randomization plan?
-
Therneau, T. M. (1993) How many stratification factors are "too many" to use in a randomization plan? Controlled Clinical Trials 14, 98-108.
-
(1993)
Controlled Clinical Trials
, vol.14
, pp. 98-108
-
-
Therneau, T.M.1
-
223
-
-
33750852210
-
Dose Finding in Drug Development
-
New York: Springer
-
Ting, N. (2006). Dose Finding in Drug Development. New York: Springer.
-
(2006)
-
-
Ting, N.1
-
224
-
-
1842826262
-
On the inefficiency of the adaptive design for monitoring clinical trials
-
Tsiatis, A. A. and Mehta, C. (2003). On the inefficiency of the adaptive design for monitoring clinical trials. Biometrika 90, 367-378.
-
(2003)
Biometrika
, vol.90
, pp. 367-378
-
-
Tsiatis, A.A.1
Mehta, C.2
-
225
-
-
0032418728
-
A proportional hazards model taking account of long-term survivors
-
Tsodikov, A. (1998). A proportional hazards model taking account of long-term survivors. Biometrics 54, 1508-1516.
-
(1998)
Biometrics
, vol.54
, pp. 1508-1516
-
-
Tsodikov, A.1
-
226
-
-
0036089659
-
A randomized trial comparing paroxetine and venlafaxine in the treatment of bipolar depressed patients taking mood stabilizers
-
Vieta, E., Martinez-Aran, A., Goikolea, J. M., Torrent, C, Colom, F., Benabarre, A., and Reinares, M. (2002). A randomized trial comparing paroxetine and venlafaxine in the treatment of bipolar depressed patients taking mood stabilizers. Journal of Clinical Psychiatry 63, 508-512.
-
(2002)
Journal of Clinical Psychiatry
, vol.63
, pp. 508-512
-
-
Vieta, E.1
Martinez-aran, A.2
Goikolea, J.M.3
Torrent, C.4
Colom, F.5
Benabarre, A.6
Reinares, M.7
-
227
-
-
0022771046
-
Sample sizes in the multivariate analysis of repeated measurements
-
Vonesh, E. F and Schork, M. A. (1986). Sample sizes in the multivariate analysis of repeated measurements. Biometrics 42,601-610.
-
(1986)
Biometrics
, vol.42
, pp. 601-610
-
-
Vonesh, E.F.1
Schork, M.A.2
-
230
-
-
0031799618
-
A comparison of two methods for adaptive interim analyses in clinical trials
-
Wassmer, G. (1998). A comparison of two methods for adaptive interim analyses in clinical trials. Biometrics 54, 696-705.
-
(1998)
Biometrics
, vol.54
, pp. 696-705
-
-
Wassmer, G.1
-
231
-
-
15044354311
-
Two-dimensional dose finding in discrete dose space
-
Wang, K. and Ivanova, A. (2005). Two-dimensional dose finding in discrete dose space. Biometrics 61, 217-222.
-
(2005)
Biometrics
, vol.61
, pp. 217-222
-
-
Wang, K.1
Ivanova, A.2
-
232
-
-
0023217456
-
Approximately optimal one-parameter boundaries for group sequential trials
-
Wang, S. K. and Tsiatis, A. A. (1987). Approximately optimal one-parameter boundaries for group sequential trials. Biometrics 43,193-199.
-
(1987)
Biometrics
, vol.43
, pp. 193-199
-
-
Wang, S.K.1
Tsiatis, A.A.2
-
233
-
-
0016335739
-
Quasi-likelihood functions, generalized linear models, and the Gauss-Newton method
-
Wedderburn, R. W M. (1974). Quasi-likelihood functions, generalized linear models, and the Gauss-Newton method. Biometrika 61,439-447.
-
(1974)
Biometrika
, vol.61
, pp. 439-447
-
-
Wedderburn, R.W.M.1
-
234
-
-
0003158427
-
The adaptive biased coin design for sequential experiments
-
Wei, L. J. (1978). The adaptive biased coin design for sequential experiments. The Annals of Statistics 6,92-100.
-
(1978)
The Annals of Statistics
, vol.6
, pp. 92-100
-
-
Wei, L.J.1
-
236
-
-
0029071328
-
Bayesian decision procedures for dose determining experiments
-
Whitehead, J. and Brünier, H. (1995). Bayesian decision procedures for dose determining experiments. Statistics in Medicine 14, 885-893.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 885-893
-
-
Whitehead, J.1
Brünier, H.2
-
237
-
-
0020729398
-
Group sequential clinical trials with triangular continuation regions
-
Whitehead, J. and Stratton, I. (1983). Group sequential clinical trials with triangular continuation regions. Biometrics 39, 227-236.
-
(1983)
Biometrics
, vol.39
, pp. 227-236
-
-
Whitehead, J.1
Stratton, I.2
-
238
-
-
0032497296
-
The antihypertensiveefficacy of losarían and amlodipine assessed with office and ambulatory blood pressure monitoring
-
Wilson, T. W., Lacourcière, Y., and Barnes, C. C. (1998). The antihypertensiveefficacy of losarían and amlodipine assessed with office and ambulatory blood pressure monitoring. Canadian Medical Association Journal 159,469-476.
-
(1998)
Canadian Medical Association Journal
, vol.159
, pp. 469-476
-
-
Wilson, T.W.1
Lacourcière, Y.2
Barnes, C.C.3
-
239
-
-
0002190083
-
A simple stochastic model of tumour recurrence and its applications to data on premenopausal breast cancer
-
In: Biometrie et Analyse de Dormees Spatio-Temporelles, 12, B. Asselain, M. Boniface, C. Duby, C. Lopez, J. R Masson, and J. Tranchefort, (eds.), Société Française de Biométrie, ENSA Renned, France
-
Yakovlev, A. Y., Asselain, B., Bardou, V. J., Fourquet, A., Hoang, T., Rochefediere, A., and Tsodikov, A. D. (1993). A simple stochastic model of tumour recurrence and its applications to data on premenopausal breast cancer. In: Biometrie et Analyse de Dormees Spatio-Temporelles, 12, B. Asselain, M. Boniface, C. Duby, C. Lopez, J. R Masson, and J. Tranchefort, (eds.), pp. 66-82. Société Française de Biométrie, ENSA Renned, France.
-
(1993)
, pp. 66-82
-
-
Yakovlev, A.Y.1
Asselain, B.2
Bardou, V.J.3
Fourquet, A.4
Hoang, T.5
Rochefediere, A.6
Tsodikov, A.D.7
-
240
-
-
79952597899
-
Bayesian generalized method of moments (with discussion)
-
Rejoinder, 217-222
-
Yin, G. (2009). Bayesian generalized method of moments (with discussion). Bayesian Analysis 4, 191-208; and Rejoinder, 217-222.
-
(2009)
Bayesian Analysis
, vol.4
, pp. 191-208
-
-
Yin, G.1
-
241
-
-
84858160948
-
Phase II trial design using Bayesian adaptive randomization and predictive probability
-
Journal of the Royal Statistical Society, Series C, in press
-
Yin, G., Chen, N., and Lee, J. J. (2012). Phase II trial design using Bayesian adaptive randomization and predictive probability. Journal of the Royal Statistical Society, Series C, in press.
-
(2012)
-
-
Yin, G.1
Chen, N.2
Lee, J.J.3
-
243
-
-
33748795036
-
Bayesian dose-finding in phase I/II trials using toxicity and efficacy odds ratio
-
Yin, G., Li, Y, and Ji, Y. (2006). Bayesian dose-finding in phase I/II trials using toxicity and efficacy odds ratio. Biometrics 62, 777-784.
-
(2006)
Biometrics
, vol.62
, pp. 777-784
-
-
Yin, G.1
Li, Y.2
Ji, Y.3
-
244
-
-
80053377942
-
Stochastic generalized method of moments
-
Yin, G., Ma, Y, Liang, F., and Yuan, Y. (2011). Stochastic generalized method of moments. Journal of Computational and Graphical Statistics 20, 714-727.
-
(2011)
Journal of Computational and Graphical Statistics
, vol.20
, pp. 714-727
-
-
Yin, G.1
Ma, Y.2
Liang, F.3
Yuan, Y.4
-
245
-
-
20744447735
-
Adaptive design and estimation in randomized clinical trials with correlated observations
-
Yin, G. and Shen, Y. (2005a). Adaptive design and estimation in randomized clinical trials with correlated observations. Biometrics 61, 362-369.
-
(2005)
Biometrics
, vol.61
, pp. 362-369
-
-
Yin, G.1
Shen, Y.2
-
246
-
-
22044445098
-
Self-designing trial combining with classical group sequential monitoring
-
Yin, G. and Shen, Y. (2005b). Self-designing trial combining with classical group sequential monitoring. Journal of Biopharmaceutical Statistics 15, 667-675.
-
(2005)
Journal of Biopharmaceutical Statistics
, vol.15
, pp. 667-675
-
-
Yin, G.1
Shen, Y.2
-
247
-
-
70349776681
-
Bayesian model averaging continual reassessment method in phase I clinical trials
-
Yin, G. and Yuan, Y. (2009a). Bayesian model averaging continual reassessment method in phase I clinical trials. Journal of the American Statistical Association 104, 954-968.
-
(2009)
Journal of the American Statistical Association
, vol.104
, pp. 954-968
-
-
Yin, G.1
Yuan, Y.2
-
248
-
-
63849316345
-
Bayesian dose-finding in oncology for drug combinations by copula regression
-
Yin, G. and Yuan, Y. (2009b). Bayesian dose-finding in oncology for drug combinations by copula regression. Journal of the Royal Statistical Society, Series C 58, 211-224.
-
(2009)
Journal of the Royal Statistical Society, Series C
, vol.50
, pp. 211-224
-
-
Yin, G.1
Yuan, Y.2
-
249
-
-
70349251729
-
A latent contingency table approach to dose-finding for combinations of two agents
-
Yin, G. and Yuan, Y. (2009c). A latent contingency table approach to dose-finding for combinations of two agents. Biometrics 65, 866-875.
-
(2009)
Biometrics
, vol.65
, pp. 866-875
-
-
Yin, G.1
Yuan, Y.2
-
250
-
-
84886205959
-
Bayesian approach for adaptive design
-
In: Handbook of Adaptive Designs in Pharmaceutical and Clinical Development, A. Pong, and S.-C. Chow, (eds.), Chapter 3. Boca Raton, FL: Chapman & Hall/CRC, pp. (3-l)-(3-19)
-
Yin, G. and Yuan, Y. (2010a). Bayesian approach for adaptive design. In: Handbook of Adaptive Designs in Pharmaceutical and Clinical Development, A. Pong, and S.-C. Chow, (eds.), Chapter 3. pp. (3-l)-(3-19). Boca Raton, FL: Chapman & Hall/CRC.
-
(2010)
-
-
Yin, G.1
Yuan, Y.2
-
251
-
-
77955985612
-
Bayesian dose-finding in oncology for drug combinations by copula regression
-
Correspondence by M. Gasparini, Bailey, S. and Neuenschwander, B
-
Yin, G. and Yuan, Y. (2010b). Correspondence "Bayesian dose-finding in oncology for drug combinations by copula regression" by M. Gasparini, Bailey, S. and Neuenschwander, B. Journal of Royal Statistical Society, Series C 59, 544-546.
-
(2010)
Journal of Royal Statistical Society, Series C
, vol.59
, pp. 544-546
-
-
Yin, G.1
Yuan, Y.2
-
252
-
-
84886110014
-
Fractional dose-finding methods with incomplete outcomes in phase I clinical trials
-
Technical report, Department of Statistics and Actuarial Science at The University of Hong Kong
-
Yin, G. and Zheng, S. (2011). Fractional dose-finding methods with incomplete outcomes in phase I clinical trials. Technical report, Department of Statistics and Actuarial Science at The University of Hong Kong.
-
(2011)
-
-
Yin, G.1
Zheng, S.2
-
253
-
-
79955576108
-
A Bayesian response-adaptive covariatebalanced randomization design with application to a leukemia clinical trial
-
Yuan, Y, Huang, X., and Liu, S. (2011). A Bayesian response-adaptive covariatebalanced randomization design with application to a leukemia clinical trial. Statistics in Medicine 30, 1218-1229.
-
(2011)
Statistics in Medicine
, vol.30
, pp. 1218-1229
-
-
Yuan, Y.1
Huang, X.2
Liu, S.3
-
254
-
-
58749104211
-
Sequential continual reassessment method for twodimensional dose finding
-
Yuan, Y and Yin, G. (2008). Sequential continual reassessment method for twodimensional dose finding. Statistics in Medicine 27, 5664-5678.
-
(2008)
Statistics in Medicine
, vol.27
, pp. 5664-5678
-
-
Yuan, Y.1
Yin, G.2
-
255
-
-
70350136475
-
Bayesian dose finding by jointly modeling toxicity and efficacy as time-to-event outcomes
-
Yuan, Y and Yin, G. (2009). Bayesian dose finding by jointly modeling toxicity and efficacy as time-to-event outcomes. Journal of Royal Statistical Society, Series C 58, 719-736.
-
(2009)
Journal of Royal Statistical Society, Series C
, vol.58
, pp. 719-736
-
-
Yuan, Y.1
Yin, G.2
-
256
-
-
79960029322
-
Bayesian hybrid dose-finding design in phase I oncology clinical trials
-
Yuan, Y and Yin, G. (2011a). Bayesian hybrid dose-finding design in phase I oncology clinical trials. Statistics in Medicine 30,2098-2108.
-
(2010)
Statistics in Medicine
, vol.30
, pp. 2098-2108
-
-
Yuan, Y.1
Yin, G.2
-
257
-
-
84873378000
-
Phase I/II adaptively randomized oncology trials with combined drugs
-
Yuan, Y. and Yin, G. (2011b). Phase I/II adaptively randomized oncology trials with combined drugs. Annals of Applied Statistics 5, 924-942.
-
(2011)
Annals of Applied Statistics
, vol.5
, pp. 924-942
-
-
Yuan, Y.1
Yin, G.2
-
258
-
-
79955628630
-
On the usefulness of outcome-adaptive randomization
-
Yuan, Y and Yin, G. (2011c). On the usefulness of outcome-adaptive randomization. Journal of Clinical Oncology 29, e390-e392.
-
(2011)
Journal of Clinical Oncology
, vol.29
-
-
Yuan, Y.1
Yin, G.2
-
259
-
-
80054707561
-
Robust EM continual reassessment method in oncology dose finding
-
Yuan, Y and Yin, G. (2011d). Robust EM continual reassessment method in oncology dose finding. Journal of the American Statistical Association 106, 818-831.
-
(2011)
Journal of the American Statistical Association
, vol.106
, pp. 818-831
-
-
Yuan, Y.1
Yin, G.2
-
260
-
-
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
-
261
-
-
34247981226
-
Play the winner rule and the controlled clinical trial
-
Zelen, M. (1969). Play the winner rule and the controlled clinical trial. Journal of the American Statistical Association 64, 131-146.
-
(1969)
Journal of the American Statistical Association
, vol.64
, pp. 131-146
-
-
Zelen, M.1
-
262
-
-
84886115738
-
Foreword
-
In: Adaptive Designs. N. Flournoy and W. F. Rosenberger, (eds.), Hayward, CA: Institute of Mathematical Statistics
-
Zelen, M. and Wei, L. J. (1995). Foreword. In: Adaptive Designs. N. Flournoy and W. F. Rosenberger, (eds.), Hayward, CA: Institute of Mathematical Statistics.
-
(1995)
-
-
Zelen, M.1
Wei, L.J.2
-
263
-
-
0002639772
-
The Bayesian method of moments (BMOM): Theory and applications
-
Zellner, A. (1997). The Bayesian method of moments (BMOM): Theory and applications. Advances in Econometrics 12, 85-105.
-
(1997)
Advances in Econometrics
, vol.12
, pp. 85-105
-
-
Zellner, A.1
-
264
-
-
84867132077
-
Bayesian method of moments (BMOM) analysis of parametric and semiparametric regression models
-
In Proceedings of the Section on Bayesian Statistical Science, Alexandria, VA: American Statistical Association
-
Zellner, A., Tobias, J., and Ryu, H. (1997). Bayesian method of moments (BMOM) analysis of parametric and semiparametric regression models. In Proceedings of the Section on Bayesian Statistical Science, pp. 211-216. Alexandria, VA: American Statistical Association.
-
(1997)
, pp. 211-216
-
-
Zellner, A.1
Tobias, J.2
Ryu, H.3
-
265
-
-
33745253938
-
Response-adaptive randomization in clinical trials with continuous outcomes
-
Zhang, L. and Rosenberger, W. F. (2006). Response-adaptive randomization in clinical trials with continuous outcomes. Biometrics 62, 562-569.
-
(2006)
Biometrics
, vol.62
, pp. 562-569
-
-
Zhang, L.1
Rosenberger, W.F.2
-
266
-
-
33947654793
-
Response-adaptive randomization for survival trials: the parametric approach
-
Zhang, L. and Rosenberger, W. F. (2007). Response-adaptive randomization for survival trials: the parametric approach. Journal of Royal Statistical Society, Series C 56, 153-165.
-
(2007)
Journal of Royal Statistical Society, Series C
, vol.56
, pp. 153-165
-
-
Zhang, L.1
Rosenberger, W.F.2
-
267
-
-
34248574062
-
A generalized dropthe-loser urn for clinical trials with delayed responses
-
Zhang, L. X., Chan, W. S., Cheung, S. H., and Hu, F. (2007). A generalized dropthe-loser urn for clinical trials with delayed responses. Statistica Sinica 17, 387-409.
-
(2007)
Statistica Sinica
, vol.17
, pp. 387-409
-
-
Zhang, L.X.1
Chan, W.S.2
Cheung, S.H.3
Hu, F.4
-
268
-
-
52649154223
-
Bayesian adaptive design for targeted therapy development in lung cancer-a step toward personalized medicine
-
Zhou, X., Liu, S. Kim, E. S., Herbste, R. S., and Lee J. J. (2008). Bayesian adaptive design for targeted therapy development in lung cancer-a step toward personalized medicine. Clinical Trials 5, 181-193.
-
(2008)
Clinical Trials
, vol.5
, pp. 181-193
-
-
Zhou, X.1
Liu, S.2
Kim, E.S.3
Herbste, R.S.4
Lee, J.J.5
|