4.6 Review

Current Surgical Management of Peri-Hilar and Intra-Hepatic Cholangiocarcinoma

Journal

CANCERS
Volume 13, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13153657

Keywords

cholangiocarcinoma; intra-hepatic cholangiocarcinoma (i-CCA); peri-hilar cholangiocarcinoma (h-CCA); extended liver resection; associating liver partition and portal vein ligation for staged hepatectomy (ALPPS); portal vein embolization (PVE); trans-arterial chemoembolization (TACE); radioembolization; neoadjuvant chemoradiation; liver transplantation

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The treatment of peri-hilar and intrahepatic cholangiocarcinoma continues to evolve with different strategies and surgical approaches, including advancements in radiological and chemotherapeutic techniques. Surgical resection remains the main curative option for intrahepatic cholangiocarcinoma, with liver transplantation now being considered as a potential treatment for CCA patients thanks to recent improvements in outcomes and survival rates.
Simple Summary The treatment of peri-hilar (h-CCA) and intrahepatic (i-CCA) cholangiocarcinoma is an evolving field in hepato-pancreato-biliary surgery. Continuous development of radiological and surgical techniques currently offers different treatment strategies, ranging from traditional hepatectomies to complex approaches involving preoperative portal vein embolization or associating liver partition and portal vein ligation for staged hepatectomy. Recent advances in perioperative chemo-radiotherapy have improved patient survival and have been incorporated into transplant protocols, yielding excellent results. We report a comprehensive review of current surgical and multimodal approaches to h-CCA and i-CCA treatment. Cholangiocarcinoma accounts for approximately 10% of all hepatobiliary tumors and represents 3% of all new-diagnosed malignancies worldwide. Intrahepatic cholangiocarcinoma (i-CCA) accounts for 10% of all cases, perihilar (h-CCA) cholangiocarcinoma represents two-thirds of the cases, while distal cholangiocarcinoma accounts for the remaining quarter. Originally described by Klatskin in 1965, h-CCA represents one of the most challenging tumors for hepatobiliary surgeons, mainly because of the anatomical vascular relationships of the biliary confluence at the hepatic hilum. Surgery is the only curative option, with the goal of a radical, margin-negative (R0) tumor resection. Continuous efforts have been made by hepatobiliary surgeons in order to achieve R0 resections, leading to the progressive development of aggressive approaches that include extended hepatectomies, associating liver partition, and portal vein ligation for staged hepatectomy, pre-operative portal vein embolization, and vascular resections. i-CCA is an aggressive biliary cancer that arises from the biliary epithelium proximal to the second-degree bile ducts. The incidence of i-CCA is dramatically increasing worldwide, and surgical resection is the only potentially curative therapy. An aggressive surgical approach, including extended liver resection and vascular reconstruction, and a greater application of systemic therapy and locoregional treatments could lead to an increase in the resection rate and the overall survival in selected i-CCA patients. Improvements achieved over the last two decades and the encouraging results recently reported have led to liver transplantation now being considered an appropriate indication for CCA patients.

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