New epidemiologic trends in cholangiocarcinoma

•The incidence of intrahepatic cholangiocarcinoma (iCCA) increased in the last decades.•Mortality rates of iCCA increased in the same time.•Chronic viral liver disease remains an important risk factor for iCCA.•Emergent risk factors (obesity, diabetes, metabolic dysfunction-associated fatty liver di...

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Published inClinics and research in hepatology and gastroenterology Vol. 47; no. 9; p. 102223
Main Authors Pascale, Alina, Rosmorduc, Olivier, Duclos-Vallée, Jean-Charles
Format Journal Article
LanguageEnglish
Published Elsevier Masson SAS 01.11.2023
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ISSN2210-7401
2210-741X
2210-741X
DOI10.1016/j.clinre.2023.102223

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Summary:•The incidence of intrahepatic cholangiocarcinoma (iCCA) increased in the last decades.•Mortality rates of iCCA increased in the same time.•Chronic viral liver disease remains an important risk factor for iCCA.•Emergent risk factors (obesity, diabetes, metabolic dysfunction-associated fatty liver disease - MAFLD) are increasingly associated with iCCA. Cholangiocarcinoma (CCA) is the most common biliary tract malignancy and the second most frequent primary hepatic malignancy after hepatocellular carcinoma. During the past three decades, the incidence of intrahepatic cholangiocarcinoma (iCCA) has risen in Western Europe, while the incidence of extrahepatic cholangiocarcinoma (eCCA) has remained stable or fallen. The mortality rates of iCCA, which are greater than those of eCCA, showed also an increasing trend, while those of eCCA remained stable. Well-known risk factors like hepatobiliary flukes, hepatolithiasis and choledochal cysts are important in the development of iCCA particularly in Asian countries. In Western countries, the primary sclerosing cholangitis is the most common risk factor for CCA. Hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and cirrhosis are considered to be risk factors for iCCA. Emergent risk factors such as obesity, diabetes and MAFLD are increasingly associated mostly with iCCA.
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ISSN:2210-7401
2210-741X
2210-741X
DOI:10.1016/j.clinre.2023.102223