Literature DB >> 15335285

Pharmacogenomics and stomach cancer.

Giuseppe Toffoli1, Erika Cecchin.   

Abstract

In subgroups of gastric cancer patients, chemotherapy treatments carry a high risk of toxicity without any clear evidence of antitumor activity. Individualization of therapy is required to treat each patient with the optimal drug and dose. Genetic polymorphisms are the hereditary determinants for interindividual variations of drug effect and the genetic approach represents a new tool to design a tailored therapy. This review focuses on the relevance of the host polymorphisms involved in metabolism, cellular transport and interaction with molecular targets of the drugs used in gastric cancer in conventional or innovative chemotherapy regimens. Pharmacogenetic studies based on a single gene or multi-gene approach (pharmacogenomics) are promising to identify gastric cancer patients at risk for adverse toxicity, but larger and controlled studies are needed to justify changes in the chemotherapeutic strategies.

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Year:  2004        PMID: 15335285     DOI: 10.1517/14622416.5.6.627

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  3 in total

Review 1.  Molecular markers for gastric adenocarcinoma: an update.

Authors:  Casandra Anderson; Amar Nijagal; Joseph Kim
Journal:  Mol Diagn Ther       Date:  2006       Impact factor: 4.074

Review 2.  Docetaxel: in gastric cancer.

Authors:  Emma D Deeks; Lesley J Scott
Journal:  Drugs       Date:  2007       Impact factor: 9.546

3.  DPYD*5 gene mutation contributes to the reduced DPYD enzyme activity and chemotherapeutic toxicity of 5-FU: results from genotyping study on 75 gastric carcinoma and colon carcinoma patients.

Authors:  Hong Zhang; You-ming Li; Hao Zhang; Xi Jin
Journal:  Med Oncol       Date:  2007       Impact factor: 3.064

  3 in total

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