نتایج جستجو برای: irinotecan

تعداد نتایج: 4284  

2017
Yoshito Komatsu Yutaka Takahashi Yutaka Kimura Hisashi Oda Yusuke Tajima Shigeyuki Tamura Jo Sakurai Takehiro Wakasugi Shigeru Tatebe Masahiro Takahashi Yuh Sakata Masaki Kitajima Junichi Sakamoto Shigetoyo Saji

Objective: The pharmacokinetics of irinotecan vary markedly between individuals. This study sought to compare tailored irinotecan plus S-1 therapy with S-1 monotherapy for the treatment of patients with advanced/recurrent gastric cancer. Methods: Patients with advanced/recurrent gastric cancer were randomized to receive tailored irinotecan plus S-1 (arm A) or S-1 alone (arm B). Arm A received S...

2004
Clinton F. Stewart Markos Leggas John D. Schuetz John C. Panetta Pamela J. Cheshire Jennifer Peterson Najat Daw Jesse J. Jenkins Richard Gilbertson Glen S. Germain Franklin C. Harwood Peter J. Houghton

As a single agent the ERBB1 inhibitor, gefitinib (Iressa; ZD1839) showed minimal activity against a panel of 10 pediatric tumor xenografts that do not express the ERBB1 receptor. However, combined with irinotecan (CPT-11), significantly greater than additive activity was observed in four of eight models (P < 0.05), and the combination showed enhanced activity against three additional tumor line...

2015
K. Trumpi B.L. Emmink A.M. Prins M.G.H. van Oijen P.J. van Diest C.J.A. Punt M. Koopman O. Kranenburg I.H.M. Borel Rinkes

BACKGROUND Active efflux of irinotecan by ATP-binding cassette (ABC)-transporters, in particular ABCB1 and ABCG2, is a well-established drug resistance mechanism in vitro and in pre-clinical mouse models, but its relevance in colorectal cancer (CRC) patients is unknown. Therefore, we assessed the association between ABC-transporter expression and tumour response to irinotecan in patients with m...

Journal: :Anticancer research 2008
E Wöll T Kühr W Eisterer K Gattringer R Greil A Zabernigg W Hilbe J Thaler

BACKGROUND The aim of the study was to evaluate the feasibility and efficacy of an outpatient oxaliplatin/irinotecan chemotherapy in chemonaive patients suffering from unresectable gastric cancer. MATERIALS AND METHODS Biweekly oxaliplatin (85 mg/m2) and irinotecan (125 mg/m2) was chosen since it has been shown previously in colorectal cancer that oxaliplatin (85 mg/m2) is superior to a lower...

2007
Manousos-Georgios Pramateftakis Dimitrios Kanellos Haralampos Demetriades Ioannis Kanellos Ioannis Mantzoros Emmanouil Zacharakis Kalliopi Despoudi Stamatios Angelopoulos Georgios Koliakos Thomas Zaraboukas Dimitrios Betsis

Aim: The aim of this experimental study was to investigate the effects of intraperitoneally injected irinotecan on the healing of colonic anastomoses after colon resection. Methods: Thirty male Wistar rats were used. The rats were randomized into two groups of 15 rats each. Immediately after colonic anastomoses were performed, the rats were injected intraperitoneally with either 3 ml of 0.9% Na...

Journal: :Cancer research 2004
Clinton F Stewart Markos Leggas John D Schuetz John C Panetta Pamela J Cheshire Jennifer Peterson Najat Daw Jesse J Jenkins Richard Gilbertson Glen S Germain Franklin C Harwood Peter J Houghton

As a single agent the ERBB1 inhibitor, gefitinib (Iressa; ZD1839) showed minimal activity against a panel of 10 pediatric tumor xenografts that do not express the ERBB1 receptor. However, combined with irinotecan (CPT-11), significantly greater than additive activity was observed in four of eight models (P < 0.05), and the combination showed enhanced activity against three additional tumor line...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2008
B Glimelius H Sørbye L Balteskard P Byström P Pfeiffer K Tveit R Heikkilä N Keldsen M Albertsson H Starkhammar H Garmo A Berglund

BACKGROUND To compare irinotecan with the Nordic 5-fluorouracil (5-FU) and folinic acid (FA) bolus schedule [irinotecan 180 mg/m(2) on day 1, 5-FU 500 mg/m(2) and FA 60 mg/m(2) on day 1 and 2 (FLIRI)] or the Lv5FU2 schedule [irinotecan 180 mg/m(2) on day 1, FA 200 mg/m(2), 5-FU bolus 400 mg/m(2) and infused 5-FU 600 mg/m(2) on day 1 and 2 (Lv5FU2-IRI)] due to uncertainties about how to administ...

2013
Prasad Neerati Yakkanti A. Sudhakar Jagat R Kanwar

STUDY BACKGROUND Studies on p-glycoprotein was carried out world vide with cell lines like Caco2, MDR1-LLC-PK1 and MDR1-MDCK in-vitro, but most of the results were failed to produce similar results in-vivo. In the present study curcumin inhibitory action on p-glycoprotein increased permeability of irinotecan, so in the colon cancer it would be beneficial if curcumin used as add on therapy. ME...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009
Henry S Friedman Michael D Prados Patrick Y Wen Tom Mikkelsen David Schiff Lauren E Abrey W K Alfred Yung Nina Paleologos Martin K Nicholas Randy Jensen James Vredenburgh Jane Huang Maoxia Zheng Timothy Cloughesy

PURPOSE We evaluated the efficacy of bevacizumab, alone and in combination with irinotecan, in patients with recurrent glioblastoma in a phase II, multicenter, open-label, noncomparative trial. PATIENTS AND METHODS One hundred sixty-seven patients were randomly assigned to receive bevacizumab 10 mg/kg alone or in combination with irinotecan 340 mg/m(2) or 125 mg/m(2) (with or without concomit...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2003
H J Mackay M Hill C Twelves R Glasspool T Price S Campbell A Massey M A Macham M Uzzel S M Bailey C Martin D Cunningham

BACKGROUND The aim of this study was to determine the maximum tolerated dose (MTD), toxicity profile and response rate of the oral 5-fluorouracil prodrug UFT (tegafur/uracil) and leucovorin (LV) in combination with irinotecan in patients with advanced or metastatic colorectal cancer. PATIENTS AND METHODS Patients with histologically proven advanced or metastatic colorectal adenocarcinoma rece...

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