Redifferentiation Effect of Larotrectinib for Fusion-Positive Pediatric Thyroid Cancer and Outcomes After Therapy.

J Endocr Soc

Department of Endocrine Neoplasia and Hormonal Disorders and Department of Pediatrics-Patient Care, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Published: August 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12209784PMC
http://dx.doi.org/10.1210/jendso/bvaf098DOI Listing

Publication Analysis

Top Keywords

fusion-positive pediatric
8
thyroid cancer
8
pediatric fusion-positive
8
pediatric ptc
8
pulmonary metastases
8
treated larotrectinib
8
months range
8
tumor shrinkage
8
larotrectinib
7
patients
7

Similar Publications

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 PDF

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 PDF

Rhabdomyosarcoma: development of molecular therapeutics under the microscope.

Expert 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 PDF

The 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