نتایج جستجو برای: irinotecan

تعداد نتایج: 4284  

2015
TZU-CHI HSU

At present, the global incidence of colorectal cancer is increasing, with numerous individuals succumbing to the disease. The standard treatment strategy for colorectal cancer is curative resection. However, a cure is rarely achieved for metastatic colorectal cancer. Currently, chemotherapy is the main treatment for metastatic and recurrent colorectal cancer. The majority of metastases or recur...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Manish A Shah Nancy Kemeny Amanda Hummer Marija Drobnjak Monica Motwani Carlos Cordon-Cardo Mithat Gonen Gary K Schwartz

PURPOSE The differentiation-related gene-1 (Drg1) is a recently identified gene down-regulated in malignancy and a putative suppressor of colorectal cancer metastases. Its expression is associated with improved survival in patients with prostate or breast cancer. Drg1 expression is also associated with resistance to irinotecan therapy in preclinical colorectal cancer models. The clinical evalua...

Journal: :Japanese journal of clinical oncology 2008
Makoto Tahara Kuniaki Shirao Narikazu Boku Kensei Yamaguchi Yoshito Komatsu Yoshitaka Inaba Tatsuhiro Arai Nobuyuki Mizunuma Taroh Satoh Hiroya Takiuchi Tomohiro Nishina Yuh Sakata

OBJECTIVE Cetuximab is a chimeric IgG1 monoclonal antibody that specifically blocks the epidermal growth factor receptor. We evaluated the efficacy and safety of cetuximab in combination with irinotecan in patients with metastatic colorectal cancer (CRC) refractory to irinotecan, oxaliplatin and fluoropyrimidines. METHODS Cetuximab was administered initially at a dose of 400 mg/m(2) followed ...

2016
Michelle A. Rudek Arvind Dasari Daniel Laheru Ping He Runyan Jin Rosalind Walker Gretchen E. Taylor Antonio Jimeno Ross C. Donehower Manuel Hidalgo Wells A. Messersmith W. Thomas Purcell

ABT-751 is an orally bioavailable sulfonamide with antimitotic properties. A nonrandomized phase 1 dose-escalation study of ABT-751 in combination with CAPIRI (capecitabine and irinotecan) and bevacizumab was conducted to define the maximum tolerated dose, dose-limiting toxicity (DLT), and pharmacokinetics in patients with advanced colorectal cancer. Patients were treated with ABT-751 daily for...

Journal: :Journal of B.U.ON. : official journal of the Balkan Union of Oncology 2013
Yue-Can Zeng Li Yu Yu-Ping Xiao Yan Xin Nai-Qian Wang Xiao-Ye Zhang Li Zhao

PURPOSE This study was conducted to determine the synergistic radiation sensitizing effects of the combination of sanazole and irinotecan in hypoxic cervical cancer HeLa human tumor cell line. METHODS The 3-(4,5 dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) assay was used to evaluate the number of surviving cells. Cell cycle was determined by flow cytometry. Surviving cell fract...

2017
Xinrong Sun Xiang Wang Wenming Feng Huihui Guo Chengwu Tang Yongliang Lu Xiaobin Xiang Ying Bao

The identification of novel survival predictors may help to improve the appropriate management of colorectal cancer (CRC). In the present study, two gene sets associated with irinotecan or oxaliplatin resistance in CRC cell lines were first identified and subsequently applied to the clinical CRC microarray dataset GSE14333. Subsequently, a 60-gene irinotecan resistance-associated signature and ...

Journal: :Molecular pharmacology 2005
Tim O Lankisch Arndt Vogel Stefan Eilermann Anette Fiebeler Britta Krone Ayse Barut Michael P Manns Christian P Strassburg

UDP glucuronosyltransferases (UGT) detoxify bilirubin and therapeutic drugs, a process influenced by single nucleotide polymorphisms (SNPs) in their structural genes and promoter elements. UGT1A1*28 is a functional UGT promoter polymorphism associated with Gilbert's disease and severe irinotecan toxicity, which also occurs in the absence of UGT1A1*28. The aim of this study was to identify and c...

2013
Matthew T Seymour Sarah R Brown Gary Middleton Timothy Maughan Susan Richman Stephen Gwyther Catherine Lowe Jennifer F Seligmann Jonathan Wadsley Nick Maisey Ian Chau Mark Hill Lesley Dawson Stephen Falk Ann O'Callaghan Kim Benstead Philip Chambers Alfred Oliver Helen Marshall Vicky Napp Phil Quirke

BACKGROUND Therapeutic antibodies targeting EGFR have activity in advanced colorectal cancer, but results from clinical trials are inconsistent and the population in which most benefit is derived is uncertain. Our aim was to assess the addition of panitumumab to irinotecan in pretreated advanced colorectal cancer. METHODS In this open-label, randomised trial, we enrolled patients who had adva...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2003
Ji-Youn Han Dae Ho Lee Hyae Young Kim Eun-A Kim Jae Jin Lee So Young Ju Eun Hee Shin Jin Soo Lee

PURPOSE Irinotecan and capecitabine have synergistic antitumor activity with distinct mechanisms of action but without overlapping major toxicity. We conducted a Phase II study to evaluate the efficacy of weekly irinotecan plus capecitabine in patients with previously treated non-small cell lung cancer (NSCLC). EXPERIMENTAL DESIGN Eligible patients had received at least one prior chemotherapy...

Journal: :Molecular cancer therapeutics 2009
Francesco Crea Elisa Giovannetti Filippo Cortesi Valentina Mey Sara Nannizzi Marielle I Gallegos Ruiz Simona Ricciardi Mario Del Tacca Godefridus J Peters Romano Danesi

Irinotecan is a topoisomerase-I (Top-I) inhibitor used for the treatment of colorectal cancer. DNA demethylating agents, including 5-azacytidine (5-aza), display synergistic antitumor activity with several chemotherapy drugs. 5-Aza may enhance irinotecan cytotoxicity by at least one of the following mechanisms: (a) Top-I promoter demethylation, (b) activation of genes involved in Top-I transcri...

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