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Safety of mTOR inhibitors in breast cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F16%3A33160433" target="_blank" >RIV/61989592:15110/16:33160433 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1080/14740338.2016.1192604" target="_blank" >http://dx.doi.org/10.1080/14740338.2016.1192604</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/14740338.2016.1192604" target="_blank" >10.1080/14740338.2016.1192604</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Safety of mTOR inhibitors in breast cancer

  • Original language description

    Introduction: Despite advances in the treatment of metastatic breast cancer, the lack of response or relapse/progression during the course of therapy continue to present a challenge towards deeper understanding of dysregulated signaling pathways in breast cancer. Consequently, there is an unmet medical need for the development of new agents to overcome the resistance to therapy and improve the treatment outcome. Areas covered: In this review, the mechanism of action and the role of intracellular PI3K/AKT/mTOR signaling pathway inhibition in breast cancer patients are described. Everolimus has been approved in combination with exemestane for the treatment of hormone-receptor-positive advanced breast cancer after failure of nonsteroidal aromatase inhibitor therapy. The aim of this paper is to focus on the safety and efficacy of mTOR inhibitors in the treatment of breast cancer. Current strategies of major adverse event management and prevention are delineated.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT13564" target="_blank" >NT13564: Predictive factors of pathologic response to neoadjuvant chemotherapy in patients with HER-2 positive or triple negative breast carcinoma</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2016

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Expert Opinion on Drug Safety

  • ISSN

    1474-0338

  • e-ISSN

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    1075-1085

  • UT code for WoS article

    000381534600009

  • EID of the result in the Scopus database