Mixed hepatocellular and cholangiocarcinoma: a rare tumor with a mix of parent phenotypic characteristics. Issue 11 (November 2016)

• Record Type: Journal Article
• Authors: Bergquist, John R.; Groeschl, Ryan T.; Ivanics, Tommy; Shubert, Christopher R.; Habermann, Elizabeth B.; Kendrick, Michael L.; Farnell, Michael B.; Nagorney, David M.; Truty, Mark J.; Smoot, Rory L.
• Is Part Of: HPB. Volume 18:Issue 11(2016)
• Page Start: 886
• Page End: 892
• Publication Date: 2016-11
• Subjects: ICC intrahepatic cholangiocarcinoma -- HCC hepatocellular carcinoma -- cHCC-CCA combined hepatocellular and intrahepatic cholangiocarcinoma -- NCDB National Cancer Data Base -- PUF participant user file -- AJCC American Joint Committee on Cancer -- CoC Commission on Cancer -- ACS American College of Surgeons -- SEER surveillance epidemiology and end results -- US United States; Liver -- Diseases -- Periodicals; Biliary tract -- Diseases -- Periodicals; Pancreas -- Diseases -- Periodicals; 616.362005
• DOI: 10.1016/j.hpb.2016.07.006
• Languages: English
• ISSNs: 1365-182X

Abstract

Abstract: Background: Intrahepatic lesions of mixed hepatocellular (HCC) and intrahepatic cholangiocellular carcinoma (ICC) histology are rare. The aim was to describe the natural history of these tumors relative to monomorphic ICC or HCC utilizing the National Cancer Data Base (NCDB). Methods: Patients with ICC, HCC, and mixed histology (cHCC-CCA) were identified in the NCDB (2004–2012). Inter-group comparisons were made. Kaplan–Meier and multivariable Cox Proportional Hazards analyzed overall survival. Results: The query identified 90, 499 patients with HCC; 14, 463 with ICC; and 1141 with cHCC-CCA histology. Patients with cHCC-CCA histology were relatively young (61 vs. 62 (HCC, p = 0.877) and 67 (ICC, p < 0.001) years) and more likely to have poorly differentiated tumor (29.2% vs. 10.3% (HCC) and 17.2% (ICC) p < 0.001). Median overall survival for cHCC-CCA was 7.9 months vs. 10.8 (HCC) and 8.2 (ICC, all p < 0.001). Stage-specific survival for mixed histology tumors was most similar to that of HCC for all stages. cHCC-CCA were transplanted at a relatively high rate, and transplant outcomes for mixed tumors were substantially worse than for HCC lesions. Discussion: cHCC-CCA demonstrate stage-specific survival similar to HCC, but post-surgical survival more consistent with ICC. Patients with a pre-operative diagnosis of cHCC-CCA should undergo resection when appropriate.