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Duke University

433A MSRB I103 Research Drive (Box 3156)
Durham, NC 27710
United States

Mentor Name: Zachary Reitman

Duke University

Soft tissue sarcomas (STS) represent a diverse and complex group of cancers that disproportionately affect pediatric and adolescent patients. With more than 80 different subtypes already, the list continues to expand as sequencing-based diagnostic assays become more readily available. CIC::DUX4 sarcoma is a new STS entity characterized by a novel gene fusion between CIC and DUX4. Due to the aggressive nature of the disease and the high rate of chemo-resistance, prognosis is exceptionally poor with less than half of all patients surviving beyond 5 years.

Pediatric diffuse midline gliomas (DMG) are devastating brain tumors. DMGs account for up to 10% of pediatric brain tumors and are uniformly fatal. The standard of care for DMG generally consists of radiation therapy (RT). Survival rates have not improved for at least two decades. New treatments are urgently needed to improve survival for DMG patients. Our study investigates highly therapeutically relevant molecular processes to inform future combination treatment strategies. The current studies will determine if future clinical trials should be focused on drugs that target STING.

Embryonal rhabdomyosarcoma (ERMS) is a soft tissue cancer with features of skeletal muscle, and the most common soft tissue connective cancer of childhood. While the medical community has made great strides in improving care and cure for children with ERMS, there remains a group of children with high-risk disease who only survive their cancer about one third of the time. To develop new treatments for these children, it is important to understand what mutations their ERMS tumors carry.

Mentor Name: Corinne Linardic

Mentor Name: Michael Deel

Mentor Name: Corinnr Linardic

Mentor: Corinne Linardic

Mentor: Dr. Kyle Walsh

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