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Targeting FGFR Pathways in Gastrointestinal Cancers: New Frontiers of Treatment.


ABSTRACT: In carcinogenesis of the gastrointestinal (GI) tract, the deregulation of fibroblast growth factor receptor (FGFR) signaling plays a critical role. The aberrant activity of this pathway is described in approximately 10% of gastric cancers and its frequency increases in intrahepatic cholangiocarcinomas (iCCAs), with an estimated frequency of 10-16%. Several selective FGFR inhibitors have been developed in the last few years with promising results. For example, targeting the FGFR pathway is now a fundamental part of clinical practice when treating iCCA and many clinical trials are ongoing to test the safety and efficacy of anti-FGFR agents in gastric, colon and pancreatic cancer, with variable results. However, the response rates of anti-FGFR drugs are modest and resistances emerge rapidly, limiting their efficacy and causing disease progression. In this review, we aim to explore the landscape of anti-FGFR inhibitors in relation to GI cancer, with particular focus on selective FGFR inhibitors and drug combinations that may lead to overcoming resistance mechanisms and drug-induced toxicities.

SUBMITTER: Ratti M 

PROVIDER: S-EPMC10603875 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

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Targeting FGFR Pathways in Gastrointestinal Cancers: New Frontiers of Treatment.

Ratti Margherita M   Orlandi Elena E   Hahne Jens Claus JC   Vecchia Stefano S   Citterio Chiara C   Anselmi Elisa E   Toscani Ilaria I   Ghidini Michele M  

Biomedicines 20230927 10


In carcinogenesis of the gastrointestinal (GI) tract, the deregulation of fibroblast growth factor receptor (FGFR) signaling plays a critical role. The aberrant activity of this pathway is described in approximately 10% of gastric cancers and its frequency increases in intrahepatic cholangiocarcinomas (iCCAs), with an estimated frequency of 10-16%. Several selective FGFR inhibitors have been developed in the last few years with promising results. For example, targeting the FGFR pathway is now a  ...[more]

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