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Background: Misclassification of Klatskin tumor as intrahepatic rather than extrahepatic bile duct cancer (eBDC) may overestimate the incidence of intrahepatic BDC (iBDC). This study aimed to investigate the impact of misclassified Klatskin tumor on iBDC and eBDC incidences in Korea, where BDC is highly endemic.
Methods: The data of incidence, topography and morphology code of BDC from 1999 to 2017 were obtained from the Korea Central Cancer Registry, which covers the entire 51.6 million Korean population. For misclassification analysis, all Klatskin tumors were reclassified as eBDC.
Results: Klatskin tumors accounted for 13.5% of all 81 414 BDC cases. In the registry, an average of 59.7% of Klatskin tumors were classified as iBDC, gradually decreasing from 95.5% to 16.9%. Misclassification led to a 17.3% overestimation of iBDC cases and a 15.0% underestimation of eBDC cases on average. After reclassification, age standardized rate (ASR) of incidence per 100 000 population decreased in iBDC from 3.4 to 2.9 and increased in eBDC from 2.8 to 3.2. Average annual percentage change of iBDC and eBDC incidences were 2.0% and 1.2%, respectively, but ASR of iBDC significantly decreased since 2012 (P < 0.0001).
Conclusions: Misclassification of Klatskin tumors has remarkable impact on the incidence of iBDC and eBDC in a highly endemic country.
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http://dx.doi.org/10.1002/jhbp.916 | DOI Listing |
J Gastrointest Surg
September 2025
Digestive Health Institute, AdventHealth Tampa, Florida. Electronic address:
Anticancer Res
September 2025
Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand;
Background/aim: Perihilar cholangiocarcinoma (pCCA) is an aggressive bile duct cancer with a poor prognosis (10-40% 5-year survival after resection), that is mostly found in Thailand and has limited prognostic models. Copy neutral loss of heterozygosity (cnLOH) in various cancers affects their progression leading to poorer overall survival. This study aimed to explore cnLOH patterns in individual pCCA patients in order to develop a predictive model for prognostic biomarkers.
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August 2025
Transplant Oncology Research Group, Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
Pak J Pharm Sci
August 2025
Department of Hepatobiliary Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, China/Institute of Hepato-Biliary-Pancreatic-Intestinal Disease, North Sichuan Medical College, Nanchong, China.
Hilar cholangiocarcinoma (HCCA), a malignant bile duct tumor, has an obscure pathogenesis. We aimed to assess the therapeutic effects of surgery and chemotherapy combined with the PD-1 inhibitor camrelizumab on HCCA patients' prognosis. This study included 26 HCCA patients.
View Article and Find Full Text PDFBMJ Case Rep
July 2025
Rahmah Academy of Research Excellence (RARE), Islamabad, Islamabad Capital Territory, Pakistan
Hilar cholangiocarcinoma, a rare bile duct malignancy, typically metastasises to the liver, lungs or lymph nodes, with ovarian involvement being exceedingly rare. We present a case of a South Asian woman in her mid-30s with abdominal pain, constipation, right upper quadrant discomfort and fever. Imaging and histopathological analysis of biopsy confirmed a hilar mass with ovarian metastasis, supported by elevated CA 19-9 levels.
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