Zobrazeno 1 - 10
of 37
pro vyhledávání: '"R. Thödtmann"'
Autor:
R Thödtmann, Josef Thaler, Peter Wohlmuth, Renate Schaberl-Moser, M Jagoditsch, Günther G. Steger, Raimund Jakesz, Hans Rabl, Friedrich Hofbauer, Richard Greil, Michael Gnant, F. Herbst, Hellmut Samonigg, Joerg Tschmelitsch, Walter Schippinger
Publikováno v:
British Journal of Cancer
The purpose of this trial was to investigate the efficacy of adjuvant chemotherapy with 5-fluorouracil (5-FU) and leucovorin (LV) in stage II colon cancer. Patients with stage II colon cancer were randomised to either adjuvant chemotherapy with 5-FU/
Autor:
Herlinde Dumez, J. Blatter, A. van Oosterom, Axel-R. Hanauske, R. D. Johnson, R. Thödtmann, H. Depenbrock
Publikováno v:
Journal of Clinical Oncology. 17:3009-3016
PURPOSE: Multitargeted antifolate (MTA; LY231514) has broad preclinical antitumor activity and inhibits a variety of intracellular enzymes involved in the folate pathways. This study was designed to (1) determine the maximum-tolerated dose (MTD), dos
Autor:
R, Greil, R, Thödtmann
Publikováno v:
Annals of Oncology. 18:ii86-ii88
Publikováno v:
Critical Reviews in Neurosurgery. 7:193-197
Autor:
Axel-R. Hanauske, T. Sauter, R. Thödtmann, L. Weissbach, J. Blatter, S. Weinknecht, Ute Ohnmacht
Publikováno v:
Investigational new drugs. 21(3)
Background. Metastatic renal cell carcinoma (RCC) is rising in incidence but remains difficult to treat. This clinical trial evaluated the effects of pemetrexed (multitargeted antifolate, ALIMTA®) for the treatment of metastatic RCC. Patients and me
Autor:
A.H.G.J Schrijvers, R Thödtmann, Ahmad Awada, Martine Piccart, Axel-R. Hanauske, Jantien Wanders, I.M. von Broen
Publikováno v:
European journal of cancer (Oxford, England : 1990). 39(6)
A single-agent dose-escalating phase I and pharmacokinetic study on the naphthalamide agent, LU 79553, was performed to determine its safety profile, maximum tolerated dose (MTD) and recommended dose for phase II studies. LU 79553 was given intraveno
Publikováno v:
Seminars in oncology. 26(2 Suppl 6)
MTA (multitargeted antifolate, LY231514) is a novel antimetabolite resulting from structure/activity studies of the lometrexol-type antifolates. It has been shown to inhibit various enzymes of folate pathways and has broad antitumor activity in a var
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 40(11)
PET using 18F-fluorodeoxyglucose (FDG) is increasingly applied to monitor the response of malignant tumors to radiotherapy and chemotherapy. The aim of this study was to assess the reproducibility of serial FDG PET measurements to define objective cr
Autor:
Axel-R. Hanauske, Wolfgang E. Berdel, Ch. Manegold, K. Burk, A. Kaeser-Fröhlich, Andreas Hüttmann, Rassmann I, H.H. Fiebig, R. Thödtmann, M. Mross
Publikováno v:
Investigational new drugs. 16(4)
Background: NK611 is a novel podophyllotoxin derivative. Compared with etoposide, NK611 carries a dimethyl-amino group at the D-glucose moiety. The antitumor activity of NK611 showed to be equal or superior to etoposide in a variety of in vitro and i
Autor:
W, Römer, A R, Hanauske, S, Ziegler, R, Thödtmann, W, Weber, C, Fuchs, W, Enne, M, Herz, C, Nerl, M, Garbrecht, M, Schwaiger
Publikováno v:
Blood. 91(12)
Positron emission tomography (PET) using F-18 fluorodeoxyglucose (FDG) was performed in non-Hodgkin's lymphoma (NHL), which is known to be highly responsive to chemotherapy, but also yields variable treatment results to answer the following questions