Cargando…

Prolonged Survival of a Patient with Advanced-Stage Combined Hepatocellular-Cholangiocarcinoma

Combined hepatocellular-cholangiocarcinoma (cHCC/CCA) represents a rare type of primary liver cancer with a very limited prognosis. Although just recently genomic studies have contributed to a better understanding of the disease's genetic landscape, therapeutic options, especially for advanced-...

Descripción completa

Detalles Bibliográficos
Autores principales: Loosen, Sven H., Gaisa, Nadine T., Schmeding, Maximilian, Heining, Christoph, Uhrig, Sebastian, Wirtz, Theresa H., Kalverkamp, Sebastian, Spillner, Jan, Tacke, Frank, Stenzinger, Albrecht, Glimm, Hanno, Fröhling, Stefan, Trautwein, Christian, Roderburg, Christoph, Longerich, Thomas, Neumann, Ulf Peter, Luedde, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772835/
https://www.ncbi.nlm.nih.gov/pubmed/33442346
http://dx.doi.org/10.1159/000511034
Descripción
Sumario:Combined hepatocellular-cholangiocarcinoma (cHCC/CCA) represents a rare type of primary liver cancer with a very limited prognosis. Although just recently genomic studies have contributed to a better understanding of the disease's genetic landscape, therapeutic options, especially for advanced-stage patients, are limited and often experimental, as no standardized treatment protocols have been established to date. Here, we report the case of a 38-year-old male patient who was diagnosed with extensive intrahepatic cHCC/CCA in an otherwise healthy liver without signs of chronic liver disease. An interdisciplinary stepwise therapeutic approach including locoregional liver-targeted therapy, systemic chemotherapy, liver transplantation, surgical pulmonary metastasis resection, and next-generation sequencing-based targeted therapy led to a prolonged overall survival beyond 5 years with an excellent quality of life. This case report comprises several provocative treatment decisions that are extensively discussed in light of the existing literature on this rare but highly aggressive malignancy.