Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Isabelle Hennebelle"'
Autor:
Pauline Claraz, Elina Wolff, Florent Puisset, Charlotte Vert, Isabelle Riff, Jean-Marie Canonge, Isabelle Hennebelle, Anaïs Grand, Sophie Perriat, Yann Cretu
Publikováno v:
American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists. 77(22)
Purpose Infusion of cytotoxic drugs carries the risk of occupational exposure of healthcare workers. Since disconnecting an infusion line is a source of contamination, flushing of tubing after infusion of cytotoxic agents is recommended, but the opti
Autor:
C. Garnier Tixidre, Caroline Delmas, J.-P. Delord, Etienne Chatelut, Isabelle Lochon, Agnes Bonadona, Anthony Goncalves, Nicolas Penel, Fabienne Thomas, Isabelle Hennebelle, C. Dhelens, Christine Toulas
Publikováno v:
Clinical Pharmacology & Therapeutics. 99:235-242
Despite the growing evidence that dihydropyrimidine dehydrogenase deficiency (DPD, encoded by the DPYD gene) confers a higher risk of developing severe toxicity, most patients are not screened for DPD deficiency before fluoropyrimidine treatment. We
Autor:
Jean-Marc Soulat, Aude Levant-Herin, Isabelle Hennebelle, Dana Macovei, Maguy Metais, Monique Marpinard, Yann Cretu
Publikováno v:
Archives des Maladies Professionnelles et de l'Environnement. 79:339-340
Objet Dans la continuite des recommandations pour la manipulation des cytotoxiques debutees en 2013, la derniere etape est constituee par l’elimination des dechets de chimiotherapie et la mise en place de kit d’intervention en cas d’epanchement
Autor:
Isabelle Hennebelle, Christine Chevreau, Sarah Bétrian, Etienne Chatelut, Sophie Le Guellec, Fabienne Thomas, Anne-Pascale Laurenty, Chantal Le Guellec
Publikováno v:
Pharmacogenomics. 14:1389-1396
We describe here the case of a 60-year old male patient treated for an extensive local progression of a pleiomorphic sarcoma on the right tibial crest with second-line trabectedin. Two cycles were administrated before a major liver toxicity was retri
Autor:
Chaza El Hannani, Isabelle Hennebelle, Roger Faroux, Mireille Francoual, Eric Francois, J.H. Jacob, Gérard Milano, Marie-Christine Etienne-Grimaldi, Jean-Louis Formento, Jaafar Bennouna, Jean-Yves Douillard, Etienne Chatelut
Publikováno v:
British Journal of Clinical Pharmacology. 73:776-785
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Previous pharmacogenetic studies have reported the potential predictive value of thymidylate synthase (TYMS) polymorphisms or methylenetetrahydrofolate reductase (MTHFR) polymorphisms for the efficacy of 5
Autor:
Melanie White-Koning, Jean Pierre Delord, Fabienne Thomas, Gilles Vassal, Etienne Chatelut, Elodie Civade, Marie-Cécile Le Deley, Birgit Geoerger, Isabelle Hennebelle
Publikováno v:
Clinical Cancer Research. 17:4862-4871
Purpose: The aim of this pharmacokinetic–pharmacodynamic (PK–PD) analysis was to evaluate the pharmacologic characteristics of erlotinib and its main metabolite (OSI-420) in pediatric patients compared with those in adult patients. Experimental D
Autor:
Adil Benlyazid, Etienne Chatelut, Fabienne Thomas, Isabelle Hennebelle, Melanie White-Koning, Philippe Rochaix, Jean Pierre Delord, Jean-Louis Lefebvre, Jérôme Sarini, Laurence Malard
Publikováno v:
European Journal of Cancer. 45:2316-2323
A clinical study was conducted to determine the safety and efficacy of neoadjuvant erlotinib treatment in patients with head and neck squamous cell carcinoma [Thomas F, Rochaix P, Benlyazid A, et al. Pilot study of neoadjuvant treatment with erlotini
Publikováno v:
Anti-Cancer Drugs. 12:741-751
The in vitro and in vivo combination of oxaliplatin and irinotecan was investigated in a panel of four human colon cancer cell lines and their counterpart xenografts. In vitro and in vivo experiments demonstrated a synergistic or additive interaction
Autor:
Pierre Canal, Catherine Terret, Etienne Chatelut, Sylvie Guichard, Isabelle Hennebelle, Roland Bugat
Publikováno v:
Anti-Cancer Drugs. 11:465-470
Irinotecan (CPT-11) is a topoisomerase I inhibitor commonly used in the treatment of colorectal tumors. It is a prodrug, converted to an active metabolite, SN-38, by carboxylesterases (CEs). CEs are ubiquitary enzymes that react with numerous substra
Autor:
P Chevreau, Sylvie Guichard, Isabelle Hennebelle, Etienne Chatelut, Janick Selves, Isabelle Lochon, Roland Bugat, Catherine Terret, Pierre Canal, E Frétigny
Publikováno v:
British Journal of Cancer
CPT-11 is a prodrug activated by carboxylesterases to the active metabolite SN-38 which is a potent inhibitor of topoisomerase I. CPT-11 is of clinical interest in the treatment of colorectal cancer. We evaluated the activities of CPT-11 converting c