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Published on: April 3, 2026
Achieving Stable Disease in an Adult with Malignant Gastrointestinal Tumor following Cabozantinib Treatment: Case
Brianna Jo Iverson1, Mohammed M Milhem2, John Markus Rieth2
1Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Introduction:
Malignant gastrointestinal neuroectodermal tumor (GNET) is a rare and aggressive neoplasm that is characterized by EWSR1 rearrangements. Most patients present with metastatic disease. There are no established treatment guidelines, and systemic therapy options remain poorly defined.
Case Presentation:
A woman in her late 30s presented initially with right upper quadrant pain and bloating. Endoscopic biopsy of a duodenal mass revealed a SOX10-positive malignant neoplasm. Molecular testing identified an EWSR1:CREB1 fusion, confirming GNET. Initial treatment with ipilimumab and nivolumab resulted in disease progression. Subsequent therapies included a selective interleukin-2 agonist clinical trial, nivolumab/relatlimab, and temozolomide, all associated with continued progression. Cabozantinib was initiated after further radiographic progression. Follow-up imaging demonstrated tumor regression, and the patient maintained stable disease for 15 months before mild progression.
Conclusion:
Metastatic GNET has a poor prognosis and lacks standardized systemic therapy. This case demonstrates durable disease stabilization with cabozantinib after progression on immunotherapy and chemotherapy. Tyrosine kinase inhibition may represent a promising therapeutic strategy in GNET and warrants further investigation.
Insights
Malignant gastrointestinal neuroectodermal tumor (GNET) is rare and aggressive. Cabozantinib showed durable disease stabilization in a patient with metastatic GNET, suggesting tyrosine kinase inhibitors may be a promising treatment strategy.
Area of Science:
- Oncology
- Gastroenterology
- Molecular Pathology
Background:
- Malignant gastrointestinal neuroectodermal tumor (GNET) is a rare, aggressive neoplasm.
- GNET is characterized by EWSR1 rearrangements and often presents as metastatic disease.
- Established treatment guidelines and effective systemic therapies for GNET are lacking.