Abstract
Driver mutations in the CTNNB1 gene (encoding β-catenin) are a hallmark of sporadic hepatoblastoma (HBL). Our results show that CTNNB1 circulating tumour DNA (ctDNA) is readily detected in patients diagnosed with localised HBL, with serial sampling along the course of therapy and follow up providing a sensitive mechanism to monitor tumour dynamics and response to treatment. This exciting potential for CTNNB1 ctDNA to serve as a biomarker for treatment response in HBL holds clinical value, and requires assessment in a larger cohort of mixed tumour stages and recurrent disease.
Original language | English |
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Article number | e28594 |
Number of pages | 4 |
Journal | Pediatric Blood and Cancer |
Volume | 67 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1 Nov 2020 |
Bibliographical note
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