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Updated: Apr 30, 2026

An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Sorafenib use in the transplant setting.
Giulia Castelli1, Patrizia Burra, Anna Giacomin
1Department of Surgery, Oncology, and Gastroenterology, Padua University School of Medicine, Padua, Italy.
For liver transplantation (LT) in hepatocellular carcinoma (HCC), sorafenib (SFN) use before or after LT is not currently supported by data. More research is needed to determine its efficacy and cost-effectiveness.
Area of Science:
- Hepatobiliary Surgery
- Medical Oncology
- Transplant Medicine
Background:
- Liver transplantation (LT) is a standard treatment for hepatocellular carcinoma (HCC).
- Sorafenib (SFN) is approved for advanced HCC, but its role alongside LT is unclear.
- Potential toxicities, especially with mTOR inhibitor immunosuppressants, warrant investigation.
Purpose of the Study:
- To review current evidence on the use of SFN in conjunction with LT for HCC.
- To evaluate the efficacy and cost-effectiveness of SFN in neoadjuvant, adjuvant, and recurrence settings.
- To assess the safety profile of SFN, considering potential interactions with immunosuppressants.
Main Methods:
- Systematic review of existing literature on SFN and LT for HCC.
- Analysis of studies examining SFN use before, during, and after LT.
- Evaluation of reported toxicity data and impact on immunosuppressive regimens.
Main Results:
- Current data do not support the use of SFN in the pre- or post-LT setting for HCC.
- Evidence regarding the efficacy and cost-effectiveness of SFN in combination with LT is insufficient.
- Toxicity concerns, particularly with mTOR inhibitors, require careful consideration.
Conclusions:
- The combination of SFN with LT for HCC is not currently recommended based on available evidence.
- Further clinical trials are necessary to establish the safety and efficacy of SFN in the context of LT.
- Optimal treatment strategies for advanced HCC in patients undergoing or eligible for LT require additional research.
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