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Comparison of Albumin In Situ Hybridization in Genetically Characterized Cholangiocarcinoma and Tumors of Other
Jay Shi1, Sahar Hosseini2, Evan Lang3
1Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Abstract:
Intrahepatic cholangiocarcinoma (CCA) is a rare liver cancer that is difficult to diagnose because of its morphologic and immunophenotypic overlap with metastatic tumors from other primary sites, a challenge further complicated by the liver's role as one of the most common destinations for metastatic spread. FGFR fusions and IDH1/2 mutations are characteristic of intrahepatic CCA, and recent studies have shown that inhibitors targeting these alterations significantly improve survival. However, diagnosis remains challenging and often relies on molecular techniques that are not universally available, limiting the potential impact of these therapies. Albumin messenger RNA in situ hybridization (albumin ISH) is a well-established test that aids in the diagnosis of CCA, yet its expression level has not been systematically evaluated in relation to tumor genetic background. Using a cohort of 63 CCAs and 157 tumors of other origins, we demonstrated that nearly all (93%) CCAs with FGFR fusions and IDH1/2 mutations (8 and 20 cases, respectively) showed strong albumin ISH positivity, whereas tumors with other characteristic CCA alterations in BAP1, ARID1A, or PBRM1 were less likely to be positive and showed comparatively weaker expression. These findings suggest that albumin ISH may serve as a valuable screening tool for identifying tumors with actionable targets while also posing an intriguing link between albumin expression and specific carcinogenesis pathways.
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