Targeted therapy or immunotherapy? Optimal treatment in hepatocellular carcinoma
Merly Contratto1, Jennifer Wu1
1Division of Hematology and Oncology, Perlmutter Cancer Center, New York University School of Medicine, New York, NY 10016, United States.
Abstract:
Hepatocellular carcinoma (HCC) is the fifth leading cause of cancer mortality in the United States and the second leading cause of cancer mortality worldwide. Sorafenib is the only food and drug administration (FDA) approved as first line systemic treatment in HCC. Regorafenib and nivolumab are the only FDA approved second line treatment after progression on sorafenib. We will discuss all potential first and second line options in HCC. In addition, we also will explore sequencing treatment options in HCC, and examine biomarkers that can potentially predict benefits from treatments such as immune checkpoint inhibitor. This minireview summarizes potential treatments in HCC based on clinical trials that have been published in manuscript or abstract format from 1994-2018.
Insights
Hepatocellular carcinoma (HCC) treatments are limited, with only sorafenib approved for first-line use. This review examines current and potential first- and second-line systemic therapies and biomarkers for HCC patients.
Area of Science:
- Hepatobiliary cancers
- Medical oncology
- Clinical research
Background:
- Hepatocellular carcinoma (HCC) is a major global cause of cancer death.
- Current first-line systemic treatment for HCC is limited to sorafenib.
- Second-line options after sorafenib progression include regorafenib and nivolumab.
Purpose of the Study:
- To review all potential first- and second-line systemic treatment options for HCC.
- To explore treatment sequencing strategies in HCC management.
- To examine biomarkers that may predict treatment efficacy, including for immune checkpoint inhibitors.
Main Methods:
- Literature review of clinical trials in HCC.
- Analysis of published manuscripts and abstracts from 1994-2018.
- Synthesis of data on systemic therapies and predictive biomarkers.
Main Results:
- Limited FDA-approved first- and second-line treatments currently exist for HCC.
- Various clinical trials have investigated alternative and emerging therapies.
- Biomarker research is ongoing to personalize HCC treatment selection.
Conclusions:
- There is a critical need for expanded first- and second-line treatment options for HCC.
- Understanding treatment sequencing and identifying predictive biomarkers are crucial for improving patient outcomes.
- Further research and clinical trials are essential to advance HCC therapy.
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