1. Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers.
- Author
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Franco AT, Ricarte-Filho JC, Isaza A, Jones Z, Jain N, Mostoufi-Moab S, Surrey L, Laetsch TW, Li MM, DeHart JC, Reichenberger E, Taylor D, Kazahaya K, Adzick NS, and Bauer AJ
- Subjects
- Child, Gene Fusion, Humans, Mutation, Proto-Oncogene Proteins B-raf genetics, Thyroid Cancer, Papillary genetics, Oncogenes, Thyroid Neoplasms genetics, Thyroid Neoplasms pathology
- Abstract
Purpose: In 2014, data from a comprehensive multiplatform analysis of 496 adult papillary thyroid cancer samples reported by The Cancer Genome Atlas project suggested that reclassification of thyroid cancer into molecular subtypes, RAS -like and BRAF -like, better reflects clinical behavior than sole reliance on pathologic classification. The aim of this study was to categorize the common oncogenic variants in pediatric differentiated thyroid cancer (DTC) and investigate whether mutation subtype classification correlated with the risk of metastasis and response to initial therapy in pediatric DTC., Methods: Somatic cancer gene panel analysis was completed on DTC from 131 pediatric patients. DTC were categorized into RAS -mutant ( H-K-NRAS ), BRAF -mutant ( BRAF p.V600E), and RET / NTRK fusion ( RET , NTRK1 , and NTRK3 fusions) to determine differences between subtype classification in regard to pathologic data (American Joint Committee on Cancer TNM) as well as response to therapy 1 year after initial treatment had been completed., Results: Mutation-based subtype categories were significant in most variables, including age at diagnosis, metastatic behavior, and the likelihood of remission at 1 year. Patients with RET / NTRK fusions were significantly more likely to have advanced lymph node and distant metastasis and less likely to achieve remission at 1 year than patients within RAS- or BRAF -mut subgroups., Conclusion: Our data support that genetic subtyping of pediatric DTC more accurately reflects clinical behavior than sole reliance on pathologic classification with patients with RET / NTRK fusions having worse outcomes than those with BRAF -mutant disease. Future trials should consider inclusion of molecular subtype into risk stratification., Competing Interests: Lea SurreyEmployment: Rothman Orthopedics (I) Theodore W. LaetschConsulting or Advisory Role: Novartis, Bayer, Cellectis, Aptitude Health, Clinical Education Alliance, Deciphera, Jumo Health, Massive Bio, Med Learning Group, Medscape, Physicans' Education Resource, Y-mAbs TherapeuticsResearch Funding: Pfizer (Inst), Novartis (Inst), Bayer (Inst), AbbVie (Inst), Amgen (Inst), Atara Biotherapeutics (Inst), Bristol Myers Squibb (Inst), Lilly (Inst), Epizyme (Inst), GlaxoSmithKline (Inst), Janssen (Inst), Jubilant Pharmaceuticals (Inst), Novella Clinical (Inst), SERVIER (Inst), Foundation Medicine (Inst), Merck Sharp & Dohme (Inst) Ken KazahayaHonoraria: Cook MedicalConsulting or Advisory Role: Cook MedicalSpeakers' Bureau: Cook MedicalExpert Testimony: US DOJ Andrew J. BauerHonoraria: Sandoz-NovartisConsulting or Advisory Role: IBSAResearch Funding: Rare Thyroid Therapeutics International AB (Inst)Travel, Accommodations, Expenses: SandozNo other potential conflicts of interest were reported.
- Published
- 2022
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