ROS1-GOPC/FIG: a novel gene fusion in hepatic angiosarcoma
Eric I Marks1, Sahithi Pamarthy2, Don Dizon1
1Division of Hematology-Oncology, Lifespan Cancer Institute, Warren-Alpert Medical School of Brown University, Providence, RI, USA.
Abstract:
Hepatic angiosarcoma (HAS) is a rare and highly lethal malignancy with few effective systemic treatments. Relatively little is known about the genetic abnormalities that drive this disease. As a result, there has been minimal progress towards applying targeted therapies to the treatment of HAS. We describe the first reported case of a patient with HAS that harbored a fusion of ROS1 with GOPC/FIG. Similar to other rearrangements involving ROS1, the resulting fusion protein is believed to act as a major driver of carcinogenesis and may be subject to inhibition by drugs that target ROS1 such as crizotinib. We then queried the MSK-IMPACT clinical sequencing cohort and cBioportal datasets, demonstrating the previously unknown prevalence of ROS1-GOPC fusions in soft tissue sarcomas and hepatobiliary cancers. Amplification of these genes was also found to correlate with reduced overall survival. This is followed by a review of the role played by ROS1 rearrangements in cancer, as well as the evidence supporting the use of targeted therapies against the resulting fusion protein. We suggest that testing for ROS1 fusion and, if positive, treatment with a targeted therapy could be considered at the time of diagnosis for patients with angiosarcoma. This report also highlights the need for further investigation into the molecular pathophysiology of this deadly disease.
Insights
A rare liver cancer, hepatic angiosarcoma (HAS), may be driven by ROS1-GOPC gene fusions. Targeting this fusion with drugs like crizotinib offers a potential new treatment avenue for HAS patients.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Hepatic angiosarcoma (HAS) is a rare, aggressive liver cancer with limited treatment options.
- The underlying genetic drivers of HAS remain largely unknown, hindering the development of targeted therapies.
Purpose of the Study:
- To report the first case of HAS with a ROS1-GOPC fusion.
- To investigate the prevalence and clinical significance of ROS1-GOPC fusions in various cancers.
- To review the role of ROS1 rearrangements in cancer and potential targeted therapies.
Main Methods:
- Case report of a patient with HAS harboring a ROS1-GOPC fusion.
- Bioinformatic analysis of clinical sequencing (MSK-IMPACT) and public (cBioPortal) datasets.
- Literature review on ROS1 rearrangements and targeted therapies.
Main Results:
- Identified a novel ROS1-GOPC fusion in a HAS patient, suggesting it as a potential driver.
- Discovered previously unrecognized prevalence of ROS1-GOPC fusions in soft tissue sarcomas and hepatobiliary cancers.
- Found that amplification of ROS1 or GOPC genes correlates with decreased overall survival.
Conclusions:
- ROS1-GOPC fusions are a potential oncogenic driver in HAS and other cancers.
- Targeted therapy against ROS1, such as crizotinib, may be effective for patients with ROS1-GOPC fusions.
- Routine testing for ROS1 fusions in angiosarcoma patients should be considered for guiding treatment decisions.
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