Impact of FGFR2 gene fusions on survival of patients with intrahepatic cholangiocarcinoma following curative intent resection
- Eee LN Buckarma,
- ,
- Mark Truty,
- David Nagorney,
- Sean Cleary,
- Michael Kendrick
- Mayo Clinic,
- Mayo Clinic Scottsdale-Phoenix, Arizona
Open access
Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 1748-1756 (9 pages)Journal (Volume, Issue Number)
HPB (Volume 24, Issue 10)Publication milestones
- Published - 10/2022
Publication status
ISSN
1365-182XPublication IDs
- Scopus: 85132708807
- PubMed: 35718679
Abstract
Background: Intrahepatic Cholangiocarcinoma (iCCA) is an aggressive cancer with diverse mutational profiles. An important molecular subtype is fibroblast growth factor receptor 2 (FGFR2) fusion. The effect of FGFR2 fusions on prognosis is unknown. Our aim was to assess the outcomes in resected CCA patients in relation to FGFR2 status. Methods: Surgically treated CCA patients from a single institution were retrospectively reviewed between 2008 and 2014. FGFR rearrangements were detected by fluorescence in situ hybridization (FISH). Data included patient demographics, tumor pathology, disease-free survival (DFS) and overall survival (OS). Results: Ninety-five patients underwent surgical resection for iCCA. Twelve (13%) of these were found to have FGFR2 fusion, none of which were treated with FGFR targeted therapy. Patients with FGFR2 fusions were found to have a longer 5-year (83 vs. 32%, p = 0.01) and 10-year (46 vs. 22%, p = 0.04) OS. Five and 10-year DFS was also increased (68 vs. 33% p = 0.04) and (68 vs. 25 %, p = 0.02,). FGFR2 fusion status was the strongest independent factor associated with improved OS (HR 0.23, 0.09–0.62, p=0.003) and DFS (HR 0.18, 0.05–0.67, p=0.01). Conclusion: Patients with CCA FGFR2 fusion have improved OS and DFS following surgical resection.
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