Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. N. Reaume"'
Autor:
S J, Hotte, G A, Bjarnason, D Y C, Heng, M A S, Jewett, A, Kapoor, C, Kollmannsberger, J, Maroun, L A, Mayhew, S, North, M N, Reaume, J D, Ruether, D, Soulieres, P M, Venner, E W, Winquist, L, Wood, J H E, Yong, F, Saad
Publikováno v:
Current oncology (Toronto, Ont.). 18
Traditionally, overall survival (os) has been considered the "gold standard" for evaluating new systemic oncologic therapies, because death is easy to define, is easily compared across disease sites, and is not subject to investigator bias. However,
Autor:
J. McGowan, M. Nurbhai, M. N. Reaume, Ian D. Graham, P.L. Moja, W K Evans, Keith O'Rourke, J. M. Grimshaw
Publikováno v:
Journal of Clinical Oncology. 25:6555-6555
6555 Background: The uptake of research findings into practice is often delayed (Antman et al. JAMA 1992). We investigated the relative role of evidence in determining clinical recommendations and practice for NSCLC. Novel chemotherapy agents (NCA) a
Autor:
Y. W. Oh, Pasi A. Jänne, J. von Pawel, Nathan Enas, M. Gottfried, Leslie Brail, M. N. Reaume, A. Sykes, T. Kaukel, L. Paz-Ares Rodriguez
Publikováno v:
Journal of Clinical Oncology. 24:7024-7024
7024 Background: The eicosanoid pathway is altered in NSCLC. Pharmacological activators of peroxisome proliferator-activated receptor-gamma (PPARγ) have been shown to inhibit lung tumors in vitro. LY293111 inhibits the eicosanoid pathway, is a PPAR
Autor:
D. A. Bedard, David J. Stewart, Scott A. Laurie, M. N. Reaume, D. L. Cutler, Stan Z. Gertler, R. Goel, M. C. Cripps, A. Rodgers, Glenwood D. Goss
Publikováno v:
Journal of Clinical Oncology. 23:7338-7338
7338 Background: A phase I study of (TZ)/(GC) combination has been completed, and the results previously presented at ESMO (Ann Oncol 15(3):198, 2004). Here, we report on this regimen’s activity in...
Autor:
R. Goel, David J. Stewart, Derek J. Jonker, Glenwood D. Goss, L. Avruch, W. P. Peters, T. A. Spencer, M. N. Reaume, Susan Dent
Publikováno v:
Journal of Clinical Oncology. 22:3078-3078
3078 Background: Exherin is a novel angiolytic VTA which specifically targets existing tumor vessels. Exherin is a cyclic pentapeptide (CHAVC) which competitively inhibits N-cadherin mediated endothelial cell, pericyte and tumor cell binding. Exherin
Publikováno v:
Journal of Clinical Oncology. 22:4545-4545
4545 Background: SCC of the bladder (SCCB), prostate (SCCP), and kidney (SCCK) remains a therapeutic challenge. Much debate exists in the literature about the ideal course of therapy. Methods: All ...