Intrahepatic cholangiocarcinoma: current perspectives

Rákkutatás · Cholangiocarcinoma · KRAS · TP53

Gemcitabine plus cisplatin improves overall survival in intrahepatic cholangiocarcinoma patients compared with gemcitabine alone

Intrahepatic cholangiocarcinoma (ICC) is the second most common malignancy arising from the liver. ICC makes up about 10% of all cholangiocarcinomas. It arises from the peripheral bile ducts within the liver parenchyma, proximal to the secondary biliary radicals. Histologically, the majority of ICCs are adenocarcinomas. Only a minority of patients (15%) present with resectable disease, with a median survival of less than 3 years. Multidisciplinary management of ICC is complicated by large differences in disease course for individual patients both across and within tumor stages. Risk models and nomograms have been developed to more accurately predict survival of individual patients based on clinical parameters. Predictive risk factors are necessary to improve patient selection for systemic treatments. Molecular differences between tumors, such as in the epidermal growth factor receptor status, are promising, but their clinical applicability should be validated. For patients with locally advanced disease, several treatment strategies are being evaluated. Both hepatic arterial infusion chemotherapy with floxuridine and yttrium‑90 embolization aim to downstage locally advanced ICC. Selected patients have resectable disease after downstaging, and other patients might benefit because of postponing widespread dissemination and biliary obstruction.

Intrahepatic cholangiocarcinoma remains a highly aggressive liver tumor with limited curative options. Understanding the efficacy of systemic therapies such as gemcitabine plus cisplatin is crucial to improve survival outcomes and inform clinical decision-making for patients who cannot undergo curative surgery.

Bizonyítékszint: Irányelv / elfogadott gyakorlat. Magas szintű klinikai elfogadottság.

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