-
1
-
-
79951823629
-
Seamless phase I/II trial design for assessing toxicity and efficacy for targeted agents
-
Hoering A, LeBlanc M, Crowley J. Seamless phase I/II trial design for assessing toxicity and efficacy for targeted agents. Clin Cancer Res. 2011 ; 17 (4). 640-46
-
(2011)
Clin Cancer Res
, vol.17
, Issue.4
, pp. 640-646
-
-
Hoering, A.1
Leblanc, M.2
Crowley, J.3
-
2
-
-
84878231796
-
-
3rd edn). Boca Raton, London, New York: CRC Press, 2012, pp. 97-106. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press
-
Hoering A, LeBlanc M, Crowley J Handbook of Statistics in Clinical Oncology. 3 rd edn). Boca Raton, London, New York: CRC Press, 2012, pp. 97-106. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press ; 2012: 97-106.
-
(2012)
Handbook of Statistics in Clinical Oncology
, pp. 97-106
-
-
Hoering, A.1
Leblanc, M.2
Crowley, J.3
-
3
-
-
84878249935
-
-
3rd edn). Boca Raton, London, New York: CRC Press, 2012, pp. 85-95. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press
-
Storer BE Handbook of Statistics in Clinical Oncology. 3 rd edn). Boca Raton, London, New York: CRC Press, 2012, pp. 85-95. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press ; 2012: 85-95.
-
(2012)
Handbook of Statistics in Clinical Oncology
, pp. 85-95
-
-
Storer, B.E.1
-
4
-
-
70450273499
-
'Classical 3+3 design' versus 'accelerated titration designs': Analysis of 270 phase I trials investigating anti-cancer agents
-
Penel N, Isambert N, Leblond P, et al. 'Classical 3+3 design' versus 'accelerated titration designs': Analysis of 270 phase I trials investigating anti-cancer agents. Invest New Drugs. 2009 ; 27: 552-56
-
(2009)
Invest New Drugs
, vol.27
, pp. 552-556
-
-
Penel, N.1
Isambert, N.2
Leblond, P.3
-
5
-
-
77949699034
-
Approaches to phase i clinical trial design focused on safety, efficiency and selected patient populations: A report from the clinical trial design task force of the National Cancer Institute investigational drug steering committee
-
Ivy P, Siu L, Garrett-Mayer E. Approaches to phase I clinical trial design focused on safety, efficiency and selected patient populations: A report from the clinical trial design task force of the National Cancer Institute investigational drug steering committee. Clin Cancer Res. 2010 ; 16: 1726-36
-
(2010)
Clin Cancer Res
, vol.16
, pp. 1726-1736
-
-
Ivy, P.1
Siu, L.2
Garrett-Mayer, E.3
-
6
-
-
84870895592
-
-
3rd edn). CRC Press, London, 2012, pp. 21-51. Crowley J Hoering A, ed. London: CRC Press
-
O'Quigley J, Iasonos A Handbook of Statistics in Clinical Oncology. 3 rd edn). CRC Press, London, 2012, pp. 21-51. Crowley J Hoering A, ed. London: CRC Press ; 2012: 21-51.
-
(2012)
Handbook of Statistics in Clinical Oncology
, pp. 21-51
-
-
O'Quigley, J.1
Iasonos, A.2
-
7
-
-
0030749549
-
Accelerated titration designs for phase i clinical trial in oncology
-
Simon R, Freidlin B, Rubenstein L. Accelerated titration designs for phase I clinical trial in oncology. et al J Natl Cancer Inst. 1997 ; 89: 1138-47
-
(1997)
Et Al J Natl Cancer Inst
, vol.89
, pp. 1138-1147
-
-
Simon, R.1
Freidlin, B.2
Rubenstein, L.3
-
8
-
-
36849035490
-
Translation of innovative designs into phase i trials
-
Rogatko A, Schoeneck D, Jonas W. Translation of innovative designs into phase I trials. et al J Clin Oncol. 2007 ; 25: 4982-86
-
(2007)
Et Al J Clin Oncol
, vol.25
, pp. 4982-4986
-
-
Rogatko, A.1
Schoeneck, D.2
Jonas, W.3
-
9
-
-
4444272419
-
Dose-finding based on efficacy-toxicity trade-offs
-
Thall PF, Cook JD. Dose-finding based on efficacy-toxicity trade-offs. Biometrics. 2004 ; 60: 684-93
-
(2004)
Biometrics
, vol.60
, pp. 684-693
-
-
Thall, P.F.1
Cook, J.D.2
-
10
-
-
84878235046
-
-
3rd edn). Boca Raton, London, New York: CRC Press, 2012, 85-95. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press
-
Mandrekar S, Sargent D Handbook of Statistics in Clinical Oncology. 3 rd edn). Boca Raton, London, New York: CRC Press, 2012, 85-95. Crowley J Hoering A, ed. Boca Raton, London, New York: CRC Press ; 85-95.
-
Handbook of Statistics in Clinical Oncology
, pp. 85-95
-
-
Mandrekar, S.1
Sargent, D.2
-
11
-
-
21844458704
-
Dose escalation trial designs based on a molecularly targeted endpoint
-
Hunsberger S, Rubinstein LV, Dancey J, Korn EL. Dose escalation trial designs based on a molecularly targeted endpoint. Stat Med. 2005 ; 24: 2171-81
-
(2005)
Stat Med
, vol.24
, pp. 2171-2181
-
-
Hunsberger, S.1
Rubinstein, L.V.2
Dancey, J.3
Korn, E.L.4
-
12
-
-
77949335209
-
The VGAMpackage for categorical data analysis
-
YeeTW. The VGAMpackage for categorical data analysis. J Stat Softw2010; 32: 1-34, http://www.jstatsoft.org/v32/i10/
-
(2010)
J Stat Softw
, vol.32
, pp. 1-34
-
-
Yee, T.W.1
-
14
-
-
0023021371
-
Global cross-ratio models for bivariate, discrete, ordered responses
-
Dale JR. Global cross-ratio models for bivariate, discrete, ordered responses. Biometrics. 1986 ; 42: 909-17
-
(1986)
Biometrics
, vol.42
, pp. 909-917
-
-
Dale, J.R.1
|