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Study focused on fusion-negative rhabdomyosarcoma in children.
Tumors analyzed from 12 patients aged 6 days to 15 years.
Utilized targeted RNA sequencing for molecular insight.
High sensitivity and specificity achieved in detecting mutations.
Most tumors found in trunk and head/neck regions.
92 percent of tumors had oncogenic alterations.
Key mutations included those in RAS pathway and DICER
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Important for future therapeutic strategies.
