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Ruff et al. Hepatoma Res 2023;9:17                              Hepatoma Research
               DOI: 10.20517/2394-5079.2023.18



               Review                                                                        Open Access



               Surgical management of intrahepatic

               cholangiocarcinoma


               Samantha M. Ruff, Timothy M. Pawlik
               Department of Surgery, Division of Surgical Oncology, The Ohio State University Wexner Medical Center and James
               Comprehensive Cancer Center, Columbus 43210, OH, USA.

               Correspondence to: Prof. Timothy M. Pawlik, Department of Surgery, The Ohio State University, Wexner Medical Center, 395
               W. 12th Ave., Suite 670, Columbus 43210, OH, USA. E-mail: tim.pawlik@osumc.edu

               How to cite this article: Ruff SM, Pawlik TM. Surgical management of intrahepatic cholangiocarcinoma. Hepatoma Res 2023;9:17.
               https://dx.doi.org/10.20517/2394-5079.2023.18

               Received: 14 Mar 2023  First Decision: 18 Apr 2023  Revised: 23 Apr 2023  Accepted: 8 May 2023  Published: 15 May 2023

               Academic Editor: Georgios Tsoulfas  Copy Editor: Yanbing Bai  Production Editor: Yanbing Bai

               Abstract
               Intrahepatic cholangiocarcinoma (ICCA) is a rare tumor with a poor prognosis that arises from the intrahepatic
               biliary tract. Patients who present with locally advanced or metastatic ICCA are generally treated with first-line
               gemcitabine/cisplatin and/or liver-directed therapy with the hope of downstaging/downsizing the disease.
               Patients who present with resectable ICCA may be treated with upfront surgery and postoperative adjuvant
               capecitabine. Staging laparoscopy should be considered to evaluate for occult metastatic disease and laparoscopic
               ultrasound can be used to better evaluate the liver parenchyma. Resection with the goal of achieving an R0 margin,
               along  with  lymphadenectomy  to  adequately  stage  patients,  should  be  the  standard  operative  approach.
               Unfortunately, the surgical technique cannot overcome poor tumor biology, and ICCA has a high incidence of
               recurrence, with many patients developing metastatic disease. Targeted therapy with IDH and FGFR inhibitors has
               had promising results in early clinical trials. Future endeavors should strive to identify more effective systemic and
               targeted therapies, which will hopefully improve survival for patients with ICCA.

               Keywords: Surgery, intrahepatic cholangiocarcinoma, margin status, lymphadenectomy




               INTRODUCTION
               Cholangiocarcinoma (CCA) is a rare tumor arising from the biliary tract that can be defined as either
               intrahepatic (ICCA) or extrahepatic (ECCA) based on its anatomic location. ICCA arises from the biliary







                           © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0
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                           adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
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