Literature DB >> 15534112

Efficacy of the novel camptothecin gimatecan against orthotopic and metastatic human tumor xenograft models.

Michelandrea De Cesare1, Graziella Pratesi, Silvia Veneroni, Raffaella Bergottini, Franco Zunino.   

Abstract

PURPOSE: Gimatecan, a novel oral lipophilic camptothecin characterized by favorable features at molecular/cellular level and by a promising profile of preclinical activity, is currently in clinical phase I/II. The aim of the study was to additionally investigate the therapeutic potential of the drug in human tumor xenografts growing in different organs as models representative of tumor growth in the clinical setting. EXPERIMENTAL
DESIGN: The models include two orthotopic central nervous system tumors, two melanomas growing intracranially, and an ovarian carcinoma growing i.p. In addition, gimatecan was tested against experimental lung metastases of two tumor types (lung and ovarian carcinomas). Gimatecan was delivered by oral gavage according to various schedules (daily or intermittent). The time (in days) mice required to show evident signs of disease was used as end point for drug efficacy.
RESULTS: Gimatecan was highly effective in delaying disease manifestations in all tumor systems investigated. In the intracranially growing tumors, a significant time increase (versus control mice) was achieved by the drug administered according to all of the schedules. In addition, almost all treated mice were alive and tumor-free at the end of the experiment in the metastatic models and in the ascitic ovarian tumor. The daily prolonged treatment schedule was the best one.
CONCLUSIONS: In all tumor systems investigated, including orthotopic tumor growth models and lung metastases, the oral administration of gimatecan showed a therapeutic benefit in terms of survival increase. The good oral availability allowed a prolonged daily treatment regimen, which seems the most promising to exploit the therapeutic potential of the drug.

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Year:  2004        PMID: 15534112     DOI: 10.1158/1078-0432.CCR-04-0962

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  6 in total

Review 1.  Camptothecin (CPT) and its derivatives are known to target topoisomerase I (Top1) as their mechanism of action: did we miss something in CPT analogue molecular targets for treating human disease such as cancer?

Authors:  Fengzhi Li; Tao Jiang; Qingyong Li; Xiang Ling
Journal:  Am J Cancer Res       Date:  2017-12-01       Impact factor: 6.166

2.  Pharmacokinetic modeling to assess factors affecting the oral bioavailability of the lactone and carboxylate forms of the lipophilic camptothecin analogue AR-67 in rats.

Authors:  Eyob D Adane; Zhiwei Liu; Tian-Xiang Xiang; Bradley D Anderson; Markos Leggas
Journal:  Pharm Res       Date:  2011-11-09       Impact factor: 4.200

3.  A phase II trial of oral gimatecan for recurrent glioblastoma.

Authors:  Jethro Hu; Patrick Y Wen; Lauren E Abrey; Camilo E Fadul; Jan Drappatz; Nadia Salem; Jeffrey G Supko; Fred Hochberg
Journal:  J Neurooncol       Date:  2012-12-12       Impact factor: 4.130

4.  An HPLC assay for the lipophilic camptothecin analog AR-67 carboxylate and lactone in human whole blood.

Authors:  Eleftheria Tsakalozou; Jamie Horn; Mark Leggas
Journal:  Biomed Chromatogr       Date:  2010-10       Impact factor: 1.902

5.  Interleukin-11 Receptor Is a Candidate Target for Ligand-Directed Therapy in Lung Cancer: Analysis of Clinical Samples and BMTP-11 Preclinical Activity.

Authors:  Marina Cardó-Vila; Serena Marchiò; Masanori Sato; Fernanda I Staquicini; Tracey L Smith; Julianna K Bronk; Guosheng Yin; Amado J Zurita; Menghong Sun; Carmen Behrens; Richard L Sidman; J Jack Lee; Waun K Hong; Ignacio I Wistuba; Wadih Arap; Renata Pasqualini
Journal:  Am J Pathol       Date:  2016-06-16       Impact factor: 4.307

6.  Gimatecan exerts potent antitumor activity against gastric cancer in vitro and in vivo via AKT and MAPK signaling pathways.

Authors:  Zuhua Chen; Zhentao Liu; Wenwen Huang; Zhongwu Li; Jianling Zou; Jingyuan Wang; Xiaoting Lin; Beifang Li; Dongshao Chen; Yanting Hu; Jiafu Ji; Jing Gao; Lin Shen
Journal:  J Transl Med       Date:  2017-12-13       Impact factor: 5.531

  6 in total

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