Échappement tumoral aux inhibiteurs de HER2: Théorie de la sédimentation

Mario Campone, Jean Sébastien Frenel, Fabrice André, Thomas Bachelot, Philippe Juin

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    1 Citation (Scopus)

    Résumé

    Twenty years have passed between the discovery of oncogene HER2, the description of its implication in mammary carcinogenesis, and the development of specific targeted therapies. To date, trastuzumab and lapatinib are the two anti-HER2 targeted therapies commonly used, demonstrating therapeutic effects. Although their clinical efficacy seems to be exclusively related to the amplification of the HER2 gene or to the overexpression of the protein, these factors are not sufficient since tumors can develop resistance. Because of a better knowledge in those mechanisms of resistance, novel therapeutic agents could help to bypass them. How should these be used with respect to current anti-HER2 targeted therapies? Recent notions such as oncogene addiction, tumor cell dormancy and residual disease led us to propose a new entity that we named the "sedimentation strategy", in which distinct targeted approaches are summed during the treatment of metastatic breast cancer patients.

    Titre traduit de la contributionTumor resistance to HER2 inhibitors: The drug sedimentation concept
    langue originaleFrançais
    Pages (de - à)665-672
    Nombre de pages8
    journalBulletin du Cancer
    Volume99
    Numéro de publication6
    Les DOIs
    étatPublié - 1 janv. 2012

    mots-clés

    • Lapatinib
    • Predictive factors
    • Resistance
    • Trastuzumab

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