4.4 Review

Non-surgical treatment of hilar cholangiocarcinoma

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WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY
卷 13, 期 11, 页码 1696-1708

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BAISHIDENG PUBLISHING GROUP INC
DOI: 10.4251/wjgo.v13.i11.1696

关键词

Cholangiocarcinoma; Interventional radiology; Oncology; Liver; Radiotherapy; Ablation

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Hilar cholangiocarcinoma, also known as Klatskin tumor, is a rare and aggressive type of cancer with poor prognosis. Surgical resection, liver transplantation, radiotherapy, chemotherapy, and minimally invasive procedures are treatment options, but only a small percentage of patients are eligible for surgery or transplant at the time of diagnosis.
Cancer of the biliary confluence also known as hilar cholangiocarcinoma (HC) or Klatskin tumor, is a rare type of neoplastic disease constituting approximately 40%-60% of intrahepatic malignancies, and 2% of all cancers. The prognosis is extremely poor and the majority of Klatskin tumors are deemed unresectable upon diagnosis. Most patients with unresectable bile duct cancer die within the first year after diagnosis, due to hepatic failure, and/or infectious complications secondary to biliary obstruction. Curative treatments include surgical resection and liver transplantation in highly selected patients. Nevertheless, very few patients are eligible for surgery or transplant at the time of diagnosis. For patients with unresectable HC, radiotherapy, chemotherapy, photodynamic therapy, and liver-directed minimally invasive procedures such as percutaneous image-guided ablation and intra-arterial chemoembolization are recommended treatment options. This review focuses on currently available treatment options for unresectable HC and discusses future perspectives that could optimize outcomes.

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