1 |
Wetherill, G. B. (1963). Sequential estimation of quantal response curves (with discussion), Journal of the Royal Statistical Society, Series B, 25, 1-48.
|
2 |
Ahn, C. (1998). An evaluation of phase I cancer clinical trial designs, Statistics in Medicine, 17, 1537-1549.
DOI
ScienceOn
|
3 |
Attia, S., Morgan-Meadows, S., Holen, K. D., Bailey, H. H., Eickhoff, J. C., Schelman, W. R., Traynor, A. M., Mulkerin, D. L., Campbell, T. C., McFarland, T. A., Huie, M. S., Cleary, J. F., Tevaarwerk, A. J., Alberti, D. B., Wilding, G. and Liu, G. (2009). Dose-escalation study of fixed-dose rate gemcitabine combined with capecitabine in advanced solid malignancies, Cancer Chemotherapy and Pharmacology, 64, 45-51.
DOI
ScienceOn
|
4 |
Tevaarwerk, A., Wilding, G., Eickhoff, J., Chappell, R., Sidor, C., Arnott, J., Bailey, H., Schelman, W. and Liu, G. (2011). Phase I study of continuous MKC-1 in patients with advanced or metastatic solid malignancies using the modified time-to-event continual reassessment method (TITE-CRM) dose escalation design, Investigative New Drugs, Published online: 12 January.
|
5 |
Rogatko, A., Babb, J. S., Tighiouart, M., Khuri, F. R. and Hudes, G. (2005). New paradigm in dose-finding trials: Patient-specific dosing and beyond phase I, Clinical Cancer Research, 11, 5342-5346.
DOI
ScienceOn
|
6 |
Tighiouart, M., Rogatko, A. and Babb, J. S. (2005). Flexible Bayesian methods for cancer phase I clinical trials: dose escalation with overdose control, Statistics in Medicine, 24, 2183-2196.
DOI
ScienceOn
|
7 |
Song, D. Y., Jones, R. J., Welsh, J. S., Haulk, T. L., Korman, L. T., Noga, S., Goodman, S., Herman, M., Mann, R., Marcellus, D., Vogelsang, G., Ambinder, R. F. and Abrams, R. A. (2003). Phase I study of escalating doses of low-dose-rate, locoregional irradiation preceding cytoxan-TBI for patients with chemotherapy-resistant non-Hodgkin's or Hodgkin's lymphoma, International Journal of Radiation Oncology, Biology, Physics, 57, 166-171.
DOI
ScienceOn
|
8 |
Storer, B. E. (1989). Design and analysis of phase I clinical trials, Biometrics, 45, 925-937.
DOI
ScienceOn
|
9 |
Storer, B. E. (2001). An evaluation of phase I clinical trial designs in the continuous dose-response setting, Statistics in Medicine, 20, 2399-2408.
DOI
ScienceOn
|
10 |
Skolnik, J. M., Barrett, J. S., Jayaraman, B., Patel, D. and Adamson, P. C. (2008). Shortening the timeline of pediatric phase I trials: The rolling six design, Journal of Clinical Oncology, 26, 190-195.
DOI
ScienceOn
|
11 |
Lee, D. P., Skolnik, J. M. and Adamson, P. C. (2005). Pediatric phase I trials in oncology: An analysis of study conduct efficiency, Journal of Clinical Oncology, 23, 8431-8441.
DOI
ScienceOn
|
12 |
Simon, R., Freidlin, B., Rubinstein, L., Arbuck, S. G. and Christian, M. C. (1997). Accelerated titration designs for phase I clinical trials in oncology, Journal of National Cancer Institute, 89, 1138-1147.
DOI
ScienceOn
|
13 |
Siu, L. L., Rowinsky, E. K., Hammond, L. A., Weiss, G. R., Hidalgo, M., Clark, G. M., Moczygemba, J., Choi, L., Linnartz, R., Barbet, N. C., Sklenar, I. T., Capdeville, R., Gan, G., Porter, C.W., Von Hoff, D. D. and Eckhardt, S. G. (2002). A Phase I and pharmacokinetic study of SAM486A, a novel polyamine biosynthesis inhibitor, administered on a daily-times-five every-three-week schedule in patients with advanced solid malignancies, Clinical Cancer Research, 8, 2157-2166.
|
14 |
Park, I. H. and Song, H. H. (1999). Estimation of maximal tolerated dose in sequential phase I clinical trials, The Korean Communications, 6, 543-564.
과학기술학회마을
|
15 |
Piantadosi, S., Fisher, J. D. and Grossman, S. (1998). Practical implementation of a modified continual reassessment method for dose-finding trials, Cancer Chemotherapy and Pharmacology, 41, 429-436.
DOI
|
16 |
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.
DOI
ScienceOn
|
17 |
O'Quigley, J., Pepe, M. and Fisher, L. (1990). Continual reassessment method: A practical design for phase I clinical trials in cancer, Biometrics, 46, 33-48.
DOI
ScienceOn
|
18 |
O'Donnell, P. V., Luznik, L., Jones, R. J., Vogelsang, G. B., Leffell, M. S., Phelps, M., Rhubart, P., Cowan, K., Piantados, S. and Fuchs, E. J. (2002). Nonmyeloablative bone marrow transplantation from partially HLA-mismatched related donors using posttransplantation cyclophosphamide, Biology of Blood and Marrow Transplantation, 8, 377-386.
DOI
ScienceOn
|
19 |
Onar-Thomas, A. and Xiong, Z. (2010). A simulation-based comparison of the traditional method, rolling-6 design and a frequentist version of the continual reassessment method with special attention to trial duration in pediatric phase I oncology trials, Contemporary Clinical Trials, 31, 259-270.
DOI
ScienceOn
|
20 |
Korn, E. L., Midthune, D., Chen, T. T., Rubinstein, L. V., Christian, M. C. and Simon, R. M. (1994). A comparison of two phase I trial designs, Statistics in Medicine, 13, 1799-1806.
DOI
ScienceOn
|
21 |
Lonial, S., Kaufman, J., Tighiouart, M., Nooka, A., Langston, A. A., Heffner, L. T., Torre, C., McMillan, S., Renfroe, H., Harvey, R. D., Lechowicz, M. J., Khoury, H. J., Flowers, C. R. and Waller, E. K. (2010). A phase I/II trial combining high-dose melphalan and autologous transplant with bortezomib for multiple myeloma: A dose- and schedule-finding study, Clinical Cancer Research, 16, 5079-5086.
DOI
|
22 |
Mick, R. and Ratain, M. J. (1993). Model-Guided determination of maximum tolerated dose in phase I clinical trials: Evidence for increased precision, Journal of the National Cancer Institute, 85, 217-223.
DOI
|
23 |
Normolle, D. and Lawrence, T. (2006). Designing dose-escalation trials with late-onset toxicities using the time-to-event continual reassessment method, Journal of Clinical Oncology, 24, 4426-4433.
DOI
ScienceOn
|
24 |
Gerke, O. and Siedentop, H. (2008). Optimal phase I dose-escalation trial designs in oncology-a simulation study, Statistics in Medicine, 27, 5329-5344.
DOI
ScienceOn
|
25 |
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.
DOI
ScienceOn
|
26 |
Kantarjian, H., Garcia-Manero, G., O'Brien, S., Faderl, S., Ravandi, F.,Westwood, R., Green, S. R., Chiao, J. H., Boone, P. A., Cortes, J. and Plunkett, W. (2010). Phase I clinical and pharmacokinetic study of oral sapacitabine in patients with acute leukemia and myelodysplastic syndrome, Journal of Clinical Oncology, 28, 285-291.
DOI
ScienceOn
|
27 |
Cheung, Y. K. and Chappell, R. (2000). Sequential designs for phase I clinical trials with late-onset toxicities, Biometrics, 56, 1177-1182.
DOI
ScienceOn
|
28 |
Dixon, W. J. and Mood, A. M. (1948). A method for obtaining and analyzing sensitivity data, Journal of the American Statistical Association, 43, 109-126.
DOI
|
29 |
Fiedler, W., Mesters, R., Heuser, M., Ehninger, G., Berdelb, W. E., Zirrgiebele, U., Robertsonf, J. D., Puchalskig, T. A., Collinsf, B., Jurgensmeierf, J. M. and Serve, H. (2010). An open-label, phase I study of cediranib (RECENTIN tm) in patients with acute myeloid leukemia, Leukemia Research, 34, 196-202.
DOI
ScienceOn
|
30 |
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.
DOI
ScienceOn
|
31 |
Babb, J. S. and Rogatko, A. (2001). Patient specific dosing in a cancer phase I clinical trial, Statistics in Medicine, 20, 2079-2090.
DOI
ScienceOn
|
32 |
Yamamoto, K., Utsunomiya, A., Tobinai, K., Tsukasaki, K., Uike, N., Uozumi, K., Yamaguchi, K., Yamada, Y., Hanada, S., Tamura, K., Nakamura, S., Inagaki, H., Ohshima, K., Kiyoi, H., Ishida, T., Matsushima, K., Akinaga, S., Ogura, M., Tomonaga, M. and Ueda, R. (2010). Phase I study of KW-0761, a defucosylated humanized anti-CCR4 antibody, in relapsed patients with adult T-cell leukemia-lymphoma and peripheral T-cell lymphoma, Journal of Clinical Oncology, 28, 1591-1598.
DOI
ScienceOn
|
33 |
Brochstein, J. A., Grupp, S., Yang, H., Pillemer, S. R. and Geba, G. P. (2010). Phase-1 study of siplizumab in the treatment of pediatric patients with at least grade II newly diagnosed acute graft-versus-host disease, Pediatric Transplantation, 14, 233-241.
DOI
ScienceOn
|