Zobrazeno 1 - 10
of 14
pro vyhledávání: '"J. J. Croles"'
Autor:
Martin Fey, Sophie D. Fosså, Linda de Prijck, Allan T. van Oosterom, Hendrik Van Poppel, Simon Horenblas, J. J. Croles, Pieter H.M. De Mulder, Martine Van Glabbeke, Gerald H. Mickisch
Publikováno v:
Cancer. 101:533-540
BACKGROUND In patients with metastatic renal cell carcinoma (MRCC), interferon-α (IFN) monotherapy leads to response rates of 5–15%, dependent on the selection of patients. In 1995, preclinical and clinical data indicated an improvement of these r
Autor:
M.A. Lentz, A. van Oosterom, P.H.M. de Mulder, A. Svedberg, Sophie D. Fosså, R. de Wit, A. Pawinski, J. J. Croles
Publikováno v:
European Journal of Cancer, 33(3), 496-499. Elsevier Ltd.
The aim of this study was to determine the objective tumour response rate and duration of response and toxicity of linomide (Roquinimex) treatment in patients with disseminated renal cell carcinoma, pretreated or not pretreated with immunotherapy. Fr
Autor:
P. A. Van Liessum, C. J. A. Punt, Y. Kamm, J. T. M. Burghouts, J. J. Croles, P.H.M. de Mulder
Publikováno v:
Cancer, 72(7), 2107-2111. John Wiley and Sons Inc.
Background 5-Fluorouracil (5-FU), when combined with leucovorin (LV) or interferon-alpha (IFN-alpha), may result in improved response rates compared with 5-FU alone in patients with advanced colorectal cancer. The authors investigated the clinical ef
Autor:
T. Skovsgaard, C.J.A. Punt, L. Hammershaimb, J. Douma, J. Schüller, J. J. Croles, J. Zhang, E. W. Muller, H. Lochs, H.J. Keizer, C. H. H. Ten Napel
Publikováno v:
Annals of Oncology, 13, 81-6
Annals of oncology, 13(1), 81-86. Oxford University Press
Annals of Oncology, 13, 1, pp. 81-6
Annals of oncology, 13(1), 81-86. Oxford University Press
Annals of Oncology, 13, 1, pp. 81-6
Item does not contain fulltext BACKGROUND: Trimetrexate (TMTX) is a biochemical modulator of 5-fluorouracil (5-FU) and leucovorin (LV). Phase II trials have shown promising activity of 5-FU/LV/TMTX in patients with advanced colorectal cancer (ACC). T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4827ac55aa0af8f3033d5953c11d28c7
http://hdl.handle.net/2066/185518
http://hdl.handle.net/2066/185518
Publikováno v:
European Journal of Cancer and Clinical Oncology. 27:755-757
The activity of cisplatin against advanced metastatic adenocarcinoma of unknown primary site (ACUP) was evaluated in 21 patients. Cisplatin (100 mg/m 2 ) was given as a 4-h continuous infusion every 3 weeks, with appropriate fluids and diuretics. The
Autor:
C. P. J. Vendrik, Jan H. Schornagel, F. Ten Kate, Richard Sylvester, J. Keizer, A.T. van Oosterom, K. Vermeylen, Jean-Pierre Droz, Ted A.W. Splinter, J. J. Croles
Publikováno v:
Germ cell tumours: 3 / Jones, W.W. [edit.]
Publisher Summary This chapter presents a preliminary report of the EORTC GU-Cooperative Group Surveillance Study. The EORTC Genito-Urinary Cooperative Group decided to start a wait-and-see policy study to see if the data from the other centers could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea94f3d52b9663ba560c8afc36926267
https://hdl.handle.net/10067/99090151162165141
https://hdl.handle.net/10067/99090151162165141
Publikováno v:
Cancer. 72(7)
5-Fluorouracil (5-FU), when combined with leucovorin (LV) or interferon-alpha (IFN-alpha), may result in improved response rates compared with 5-FU alone in patients with advanced colorectal cancer. The authors investigated the clinical efficacy of c
Publikováno v:
European journal of cancer (Oxford, England : 1990). 27(6)
The activity of cisplatin against advanced metastatic adenocarcinoma of unknown primary site (ACUP) was evaluated in 21 patients. Cisplatin (100 mg/m2) was given as a 4-h continuous infusion every 3 weeks, with appropriate fluids and diuretics. The o
Publikováno v:
European Journal of Cancer. 29:S93
Autor:
M. de Pauw, Sophie D. Fosså, G. Stoter, Richard Sylvester, J. J. Croles, Aldo V. Bono, W. G. Jones
Publikováno v:
World Journal of Urology. 4:182-185
In a phase II chemotherapy study, patients with metastatic prostate cancer were given mitomycin-C 15 mg/m2 i.v. q 6 weeks. A partial response rate of 29% was demonstrated in 31 fully evaluable patients with bidimensionally measurable metastatic depos