Mutationsbasierter therapiealgorithmus bei gastrointestinalen stromatumoren: Hat die c-Kit/PDGFRA-mutationsanalyse einflussauf ther apieentscheidungen?

Translated title of the contribution: Mutational status based therapy algorithm for gastrointestinal stroma tumors. Does c-Kit/PDGFRA mutational analysis affect treatment decisions?

N. Von Bubnoff*

*Corresponding author for this work

Abstract

Activating mutations of the stem cell factor receptor tyrosine kinase (c-Kit) or platelet-derived growth factor receptor α (PDGFRA) can be found in at least 85% of cases of gastrointestinal stromal tumors. The therapeutic options include surgery, local treatment and systemic treatment with tyrosine kinase inhibitors, such as imatinib or sunitinib. Kinase inhibitor-based treatment is used in neoadjuvant, adjuvant and metastatic settings. Knowledge of the individual mutational status allows prediction of response to first-line medical treatment and provides information which can guide selection of the appropriate second-line therapy.

Translated title of the contributionMutational status based therapy algorithm for gastrointestinal stroma tumors. Does c-Kit/PDGFRA mutational analysis affect treatment decisions?
Original languageGerman
JournalGastroenterologe
Volume7
Issue number1
Pages (from-to)30-36
Number of pages7
ISSN1861-9681
DOIs
Publication statusPublished - 01.2012

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