Zobrazeno 1 - 10
of 241
pro vyhledávání: '"B, Desoize"'
Publikováno v:
European Journal of Cancer. 32:1734-1738
The aim of this study was to validate prospectively a model of cisplatin dose adjustment. 27 patients (63 courses) with lung cancer were treated by a 5 day continuous infusion of cisplatin and etoposide. The dose of cisplatin was adjusted in order to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::375aeb0e9e1c14843a94c7a6485f29ed
https://doi.org/10.1016/0959-8049(96)00171-2
https://doi.org/10.1016/0959-8049(96)00171-2
Publikováno v:
Clinical Research and Regulatory Affairs. 11:257-268
A dose prediction method for cisplatin based on the Bayesian principle and with use of limited blood sampling is described. A reference population was used to establish plasma total platinum (Pt) pharmacokinetics. the limited sampling method, using t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cff2eda2156985022e802a44853c551
https://doi.org/10.3109/10601339409035946
https://doi.org/10.3109/10601339409035946
Autor:
J. Robert, B. Desoize
Publikováno v:
European Journal of Cancer. 30:844-851
The dose of anticancer drugs is currently adjusted to the patient body surface area, although patients have different abilities to clear anticancer drugs. The dose adjustment to physiological functions permits major toxic accidents to be avoided. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb2a5a63a236b96c8a211c0a4acb2d9
https://doi.org/10.1016/0959-8049(94)90304-2
https://doi.org/10.1016/0959-8049(94)90304-2
Publikováno v:
International journal of oncology. 5(1)
The retention of adriamycin in 5 Friend cell sublines of increasing degree of resistance was enhanced in vitro by three compounds: verapamil, nigericine and vanadate. Vanadate had the strongest activity, it enhanced also the incorporation in sensitiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f3d2cf7a06bb0ee6d6518815a7a5f06
https://pubmed.ncbi.nlm.nih.gov/21559561
https://pubmed.ncbi.nlm.nih.gov/21559561
Autor:
B, Desoize
Publikováno v:
Critical reviews in oncology/hematology. 72(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87a605dd4d0fda37609648a84dc6cbbd
https://pubmed.ncbi.nlm.nih.gov/19913213
https://pubmed.ncbi.nlm.nih.gov/19913213
Publikováno v:
Biomedicine & Pharmacotherapy. 45:203-207
Twenty-two pharmacokinetic studies were carried out in 11 patients receiving cisplatin (20 mg/m2 per d) associated with etoposide (50 mg/m2 per d), as 5-day continuous infusions, every 4 weeks. Blood was withdrawn at 8:30 am from day 1-5. Within 15 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f3b620f4a70a85e15a3c550caccc18
https://doi.org/10.1016/0753-3322(91)90109-7
https://doi.org/10.1016/0753-3322(91)90109-7
Autor:
B Desoize
Publikováno v:
Critical Reviews in Oncology/Hematology. 72:215-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b750eaf39f4b2239f809d21b70223375
https://doi.org/10.1016/j.critrevonc.2009.10.001
https://doi.org/10.1016/j.critrevonc.2009.10.001
Publikováno v:
Anticancer research. 18(6A)
Cells cultured as spheroids present an heterogeneity similar to that of tumours in vivo. In the spheroid peripheral layers, cells are proliferating, deeper cells are non-cycling, when in the aggregate centre, cells form often a necrotic core. A multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22c9e465577c20d71db896dfd7e10c3d
https://pubmed.ncbi.nlm.nih.gov/9891460
https://pubmed.ncbi.nlm.nih.gov/9891460
Autor:
B. Desoize
Publikováno v:
Critical Reviews in Oncology/Hematology. 64:208-209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9dfc3c7a9e85e44f881eb4e54b705f5
https://doi.org/10.1016/j.critrevonc.2007.09.005
https://doi.org/10.1016/j.critrevonc.2007.09.005
Publikováno v:
Anti-cancer drug design. 13(7)
Some members of a series of 12-alkyloxy benzo[c]phenanthridines are potent inhibitors of the growth of P388 tumour cells in vitro, with a strong dependence on the nature of the 12-substituent. Analogues with a quaternary nitrogen in the side chain bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::073138abc16832bc8cc6c479dd6da9af
https://pubmed.ncbi.nlm.nih.gov/9807163
https://pubmed.ncbi.nlm.nih.gov/9807163