Literature DB >> 11585970

Optimizing the use of irinotecan in colorectal cancer.

D Cunningham1, J Maroun, U Vanhoefer, E Van Cutsem.   

Abstract

The introduction of new agents with novel mechanisms of action has led to considerable changes in the management of colorectal cancer in recent years. One of these novel agents, irinotecan, has been shown to offer survival benefits in both the first- and second-line treatment of advanced/metastatic colorectal cancer. Irinotecan monotherapy improves survival compared with both best supportive care and infused 5-fluorouracil (5-FU) in patients with 5-FU-pretreated disease, without impacting negatively on patients' quality of life. As a result, irinotecan monotherapy is now considered to be the standard treatment in this setting. Irinotecan in combination with 5-FU/leucovorin (LV) was subsequently evaluated as first-line therapy for metastatic colorectal cancer in two randomized, phase III studies. Both trials confirmed that irinotecan plus infused or bolus 5-FU/leucovorin LV provide a modest survival benefit without compromising patients' quality of life. Combined irinotecan/5-FU/LV represents a new standard in the first-line treatment of metastatic colorectal cancer. In an attempt to further improve efficacy and tolerability, recent studies have investigated irinotecan in combination with capecitabine as first-line treatment for colorectal cancer. The replacement of infused 5-FU with oral capecitabine provides a more convenient treatment option. A phase I study was conducted to establish the maximum tolerated dose, and demonstrated encouraging antitumor activity and a manageable safety profile with the combination. This article provides a brief overview of the pivotal clinical trial data for irinotecan and discusses how irinotecan-based therapy may be improved in the future. It also discusses potential optimization of irinotecan use through identification of patient subpopulations most likely to benefit from combination or sequential strategies, and the potential of new, oral agents such as capecitabine to replace i.v. 5-FU as a combination partner for irinotecan.

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Year:  2001        PMID: 11585970     DOI: 10.1634/theoncologist.6-suppl_4-17

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  10 in total

1.  Caspase-mediated pro-apoptotic interaction of panaxadiol and irinotecan in human colorectal cancer cells.

Authors:  Guang-Jian Du; Chong-Zhi Wang; Zhi-Yu Zhang; Xiao-Dong Wen; Jacqueline Somogyi; Tyler Calway; Tong-Chuan He; Wei Du; Chun-Su Yuan
Journal:  J Pharm Pharmacol       Date:  2012-02-21       Impact factor: 3.765

2.  Herbal medicines as adjuvants for cancer therapeutics.

Authors:  Chong-Zhi Wang; Tyler Calway; Chun-Su Yuan
Journal:  Am J Chin Med       Date:  2012       Impact factor: 4.667

3.  Quantitative determination of irinotecan and the metabolite SN-38 by nanoflow liquid chromatography-tandem mass spectrometry in different regions of multicellular tumor spheroids.

Authors:  Xin Liu; Amanda B Hummon
Journal:  J Am Soc Mass Spectrom       Date:  2015-01-21       Impact factor: 3.109

4.  RNA-seq reveals determinants for irinotecan sensitivity/resistance in colorectal cancer cell lines.

Authors:  Xin-Xiang Li; Hong-Tu Zheng; Jun-Jie Peng; Li-Yong Huang; De-Bing Shi; Lei Liang; San-Jun Cai
Journal:  Int J Clin Exp Pathol       Date:  2014-04-15

5.  Phase I study of daily S-1 combined with weekly irinotecan in patients with advanced non-small cell lung cancer.

Authors:  Osamu Ishimoto; Takashi Ishida; Yoshihiro Honda; Mitsuru Munakata; Shunichi Sugawara
Journal:  Int J Clin Oncol       Date:  2009-02-20       Impact factor: 3.402

6.  Surefire infusion system versus standard microcatheter use during holmium-166 radioembolization: study protocol for a randomized controlled trial.

Authors:  Andor F van den Hoven; Jip F Prince; Rutger C G Bruijnen; Helena M Verkooijen; Gerard C Krijger; Marnix G E H Lam; Maurice A A J van den Bosch
Journal:  Trials       Date:  2016-10-25       Impact factor: 2.279

7.  Function of AP2/ERF Transcription Factors Involved in the Regulation of Specialized Metabolism in Ophiorrhiza pumila Revealed by Transcriptomics and Metabolomics.

Authors:  Nirin Udomsom; Amit Rai; Hideyuki Suzuki; Jun Okuyama; Ryosuke Imai; Tetsuya Mori; Ryo Nakabayashi; Kazuki Saito; Mami Yamazaki
Journal:  Front Plant Sci       Date:  2016-12-09       Impact factor: 5.753

8.  Genomic data integration by WON-PARAFAC identifies interpretable factors for predicting drug-sensitivity in vivo.

Authors:  Yongsoo Kim; Tycho Bismeijer; Wilbert Zwart; Lodewyk F A Wessels; Daniel J Vis
Journal:  Nat Commun       Date:  2019-11-06       Impact factor: 14.919

9.  Optimisation of irinotecan dose in the treatment of patients with metastatic colorectal cancer after 5-FU failure: results from a multinational, randomised phase II study.

Authors:  E Van Cutsem; L Dirix; J-L Van Laethem; S Van Belle; M Borner; M Gonzalez Baron; A Roth; R Morant; E Joosens; G Gruia; D Sibaud; H Bleiberg
Journal:  Br J Cancer       Date:  2005-03-28       Impact factor: 7.640

10.  The novel ATM inhibitor (AZ31) enhances antitumor activity in patient derived xenografts that are resistant to irinotecan monotherapy.

Authors:  Justin Greene; Anna Nguyen; Stacey M Bagby; Gemma N Jones; W M Tai; Kevin S Quackenbush; Anna Schreiber; Wells A Messersmith; Kalpana M Devaraj; Patrick Blatchford; S Gail Eckhardt; Elaine B Cadogan; Gareth D Hughes; Aaron Smith; Todd M Pitts; John J Arcaroli
Journal:  Oncotarget       Date:  2017-12-05
  10 in total

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