PMID- 35718679 OWN - NLM STAT- MEDLINE DCOM- 20221025 LR - 20221028 IS - 1477-2574 (Electronic) IS - 1365-182X (Linking) VI - 24 IP - 10 DP - 2022 Oct TI - Impact of FGFR2 gene fusions on survival of patients with intrahepatic cholangiocarcinoma following curative intent resection. PG - 1748-1756 LID - S1365-182X(22)01486-1 [pii] LID - 10.1016/j.hpb.2022.05.1341 [doi] AB - 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. CI - Copyright (c) 2022 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved. FAU - Buckarma, EeeLN AU - Buckarma E AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - De La Cruz, Gabriel AU - De La Cruz G AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - Truty, Mark AU - Truty M AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - Nagorney, David AU - Nagorney D AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - Cleary, Sean AU - Cleary S AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - Kendrick, Michael AU - Kendrick M AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. FAU - Borad, Mitesh AU - Borad M AD - Division of Hematology/Oncology, Mayo Clinic, Phoenix, AZ, USA. FAU - Graham, Rondell P AU - Graham RP AD - Division of Laboratory Medicine and Anatomic Pathology, Mayo Clinic, Rochester, MN, USA. FAU - Gores, Gregory AU - Gores G AD - Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA. FAU - Smoot, Rory AU - Smoot R AD - Department of Surgery, Mayo Clinic, Rochester, MN, USA. Electronic address: Smoot.Rory@mayo.edu. LA - eng PT - Journal Article DEP - 20220528 PL - England TA - HPB (Oxford) JT - HPB : the official journal of the International Hepato Pancreato Biliary Association JID - 100900921 RN - EC 2.7.10.1 (Receptor, Fibroblast Growth Factor, Type 2) RN - EC 2.7.10.1 (FGFR2 protein, human) SB - IM MH - Humans MH - Receptor, Fibroblast Growth Factor, Type 2/genetics/metabolism MH - *Bile Duct Neoplasms/genetics/surgery/metabolism MH - In Situ Hybridization, Fluorescence MH - Retrospective Studies MH - *Cholangiocarcinoma/genetics/surgery/metabolism MH - Gene Fusion MH - Bile Ducts, Intrahepatic/pathology EDAT- 2022/06/20 06:00 MHDA- 2022/10/26 06:00 CRDT- 2022/06/19 22:17 PHST- 2021/12/30 00:00 [received] PHST- 2022/03/17 00:00 [revised] PHST- 2022/05/23 00:00 [accepted] PHST- 2022/06/20 06:00 [pubmed] PHST- 2022/10/26 06:00 [medline] PHST- 2022/06/19 22:17 [entrez] AID - S1365-182X(22)01486-1 [pii] AID - 10.1016/j.hpb.2022.05.1341 [doi] PST - ppublish SO - HPB (Oxford). 2022 Oct;24(10):1748-1756. doi: 10.1016/j.hpb.2022.05.1341. Epub 2022 May 28.