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Context: Few data exist regarding larotrectinib therapy in pediatric fusion-positive papillary thyroid cancer (PTC), especially its effects on redifferentiation in radioactive iodine-refractory (RAIR) disease.
Objective: To describe redifferentiation effects and disease outcomes in patients with stage 2 pediatric PTC following treatment with larotrectinib ± RAI.
Methods: A retrospective case series at a tertiary cancer center of patients with fusion-positive pediatric PTC and RAIR pulmonary metastases treated with larotrectinib and considered for I therapy. Tumor response was assessed utilizing RECIST 1.1.
Results: Four patients (aged 6-16 years at PTC diagnosis; 50% female) were treated with larotrectinib 100 mg twice a day for a median of 14 months (range 6-30 months). Treatment was well tolerated, except for grade 3 hypocalcemia in 1 patient with pre-existing hypoparathyroidism. All patients had tumor shrinkage (-25% to -100%) in target and nontarget pulmonary metastases. On diagnostic I thyroid scans, any RAI uptake was identified in only 2 patients, and therapeutic I did not cause further incremental tumor shrinkage in the patients treated, despite robust pulmonary uptake on the post-therapy scans. After stopping larotrectinib and with a mean follow-up of 38 months (range 26-48 months), 2 patients had stable disease and 2 had clinically insignificant tumor progression.
Conclusion: Although larotrectinib can have a redifferentiation effect in pediatric fusion-positive PTC, therapy with I may not lead to an incremental benefit in established RAIR disease. Significant structural disease progression did not occur after cessation of larotrectinib, suggesting that a drug holiday can safely be considered in this population.
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http://dx.doi.org/10.1210/jendso/bvaf098 | DOI Listing |
Pediatr Dev Pathol
September 2025
The Hospital for Sick Children, Division of Pathology, Toronto, Canada.
Background: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood. For stratification purposes, rhabdomyosarcoma is classified into fusion-positive RMS (alveolar rhabdomyosarcoma) and fusion-negative RMS (embryonal or spindle cell/sclerosing, FN-RMS) subtypes according to its fusion status. This study aims to highlight the pathologic and molecular characteristics of a cohort of FN-RMS using a targeted NGS RNA-Seq assay.
View Article and Find Full Text PDFCancer Res Commun
September 2025
Center for Childhood Cancer Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Unlabelled: Genes encoding the RNA-binding proteins FUS, EWSR1, and TAF15 (FET proteins) are involved in chromosomal translocations in rare sarcomas. The encoded fusion oncoproteins typically include a DNA-binding domain and function as oncogenic transcription factors. FET-rearranged sarcomas are often aggressive malignancies affecting patients of all ages.
View Article and Find Full Text PDFExpert Opin Ther Targets
August 2025
Department of Pharmacology and toxicology, University of Alabama at Birmingham, Birmingham, AL, USA.
Introduction: Rhabdomyosarcoma (RMS), predominantly diagnosed in children, represents 3% of the pediatric solid tumors. RMS has characteristics of skeletal muscle, although the cell of origin remains controversial. Cytotoxic therapeutics, radiation treatment and surgery remain the standard of care; however, outcomes for advanced disease have not changed for several decades.
View Article and Find Full Text PDFThe KEAP1/NRF2 pathway, a major regulator of the cellular oxidative stress response, is frequently activated in human cancers. Often mediated by loss-of-function mutations in , this activation causes increased NRF2 transcriptional activity and constitutive activation of the antioxidant response. While mutations have been well documented in various cancers, their presence and role in thyroid carcinoma have remained largely unexplored.
View Article and Find Full Text PDF