Zobrazeno 1 - 10
of 38
pro vyhledávání: '"S. G. Arbuck"'
Autor:
S G Arbuck
Publikováno v:
Journal of Clinical Oncology. 12:233-236
Publikováno v:
Journal of Clinical Oncology. 9:2128-2133
Forty-two previously untreated patients with advanced, measurable adenocarcinoma of the pancreas were treated with weekly fluorouracil (5-FU; 600 mg/m2 intravenous [IV]) and leucovorin 500 mg/m2 IV for 6 weeks followed by a 2-week rest. A median of 1
Autor:
Z. P. Bernstein, L. Vaickus, N. Friedman, M. H. Goldrosen, H. Watanabe, R. Rahman, S. G. Arbuck, J. Sweeney, D. Vesper, E. D. Henderson, J. Zeffren, R. A. Dennin, D. Levitt, K. A. Foon
Publikováno v:
Journal of Immunotherapy. 10:141-146
We conducted a phase II study utilizing interleukin-2 (IL-2) with lymphokine-activated killer (LAK) cells as therapy for non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD). IL-2 was given at a fixed dose of 3 x 10(6) U/m2/day administered as a 2
Autor:
S G, Arbuck, J, Dancey, J M, Pluda, L, Grochow, A J, Murgo, P, Ivy, J, Wright, B, Blaylock, L E, Via, E A, Sausville
Publikováno v:
Cancer chemotherapy and biological response modifiers. 19
Biochemical correlates of mTOR inhibition by the rapamycin ester CCI-779 and tumor growth inhibition
Autor:
L, Dudkin, M B, Dilling, P J, Cheshire, F C, Harwood, M, Hollingshead, S G, Arbuck, R, Travis, E A, Sausville, P J, Houghton
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(6)
The rapamycin ester, CCI-779, potently inhibits cell growth in vitro, inhibits tumor growth in vivo, and is currently in Phase I clinical trials. To further understand the relationship between plasma systemic exposure and inhibition of the target Ser
Publikováno v:
Cancer chemotherapy and biological response modifiers. 18
Autor:
P, Therasse, S G, Arbuck, E A, Eisenhauer, J, Wanders, R S, Kaplan, L, Rubinstein, J, Verweij, M, Van Glabbeke, A T, van Oosterom, M C, Christian, S G, Gwyther
Publikováno v:
Journal of the National Cancer Institute. 92(3)
Anticancer cytotoxic agents go through a process by which their antitumor activity-on the basis of the amount of tumor shrinkage they could generate-has been investigated. In the late 1970s, the International Union Against Cancer and the World Health
Autor:
J L, Grem, J M, Sorensen, E, Cullen, C H, Takimoto, S M, Steinberg, A P, Chen, J M, Hamilton, S G, Arbuck, N, McAtee, D, Lawrence, B, Goldspiel, P G, Johnston, C J, Allegra
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 5(9)
The purpose of this study was to perform a Phase I trial of raltitrexed, a selective inhibitor of thymidylate synthase, and to determine the pharmacokinetic and toxicity profiles as a function of raltitrexed dose. Fifty patients with advanced solid t
Autor:
Francis J. Giles, M. Beran, Hai T. Tran, Bruce D. Cheson, Hagop M. Kantarjian, S. G. Arbuck, Jorge E. Cortes, Eli Estey, Carol Bivins, Norbert Vey, Susan O'Brien
Publikováno v:
Annals of oncology : official journal of the European Society for Medical Oncology. 10(5)
Summary Purpose: Topoisomerase I inhibitors have shown promising anti leukemic activity in acute myelogenous leukemia (AML) and myelodysplastic syndrome. In this phase I study, we investigated the toxicity profile, pharmacokinetics, and activity of a
Autor:
E, Fuse, H, Tanii, N, Kurata, H, Kobayashi, Y, Shimada, T, Tamura, Y, Sasaki, Y, Tanigawara, R D, Lush, D, Headlee, W D, Figg, S G, Arbuck, A M, Senderowicz, E A, Sausville, S, Akinaga, T, Kuwabara, S, Kobayashi
Publikováno v:
Cancer research. 58(15)
The pharmacokinetics of UCN-01 after administration as a 72- or 3-h infusion to cancer patients in initial Phase I trials displayed distinctive features that could not have been predicted from preclinical data. The distribution volumes (0.0796-0.158