Growth recovery in patients with <i>BRAF</i> -altered pediatric low-grade glioma following treatment with tovorafenib

Abstract Background The type II RAF inhibitor tovorafenib is US FDA-approved for patients ≥6 months of age with BRAF-altered, relapsed/refractory, pediatric low-grade glioma (pLGG). It is hypothesized that tovorafenib may inhibit CRAF within growth plate chondrocytes, slowing growth plate maturation and linear growth. This analysis investigated growth recovery after treatment with tovorafenib and factors that may impact growth recovery trajectories. Methods This was a retrospective pooled analysis of on- and off-treatment growth in children with BRAF-altered relapsed/refractory pLGG treated with tovorafenib for ≥6 months in two clinical trials and an expanded access program. Patients had to have at least one height measurement recorded &amp;gt;90 days post-treatment as of December 16, 2024. Growth suppression, recovery, and catch-up growth were derived from annualized growth velocity on and off treatment. Exposure–growth models explored growth patterns on and off treatment. Results Sixty-eight patients were included with median (range) baseline age of nine (2-16) years and median follow up 10 months post-treatment. Ninety percent of patients exhibited growth suppression during treatment, of whom 93% showed early post-treatment growth recovery and 77% showed catch-up growth. Reversible growth suppression was observed in both sexes across ages. Of 26 patients with on-treatment bone age, there was no abnormal advancement of bone age on or off treatment. Exposure–growth models suggest that younger baseline age may be associated with faster growth recovery off treatment. Conclusions Growth suppression observed with tovorafenib was reversible, with evidence of post-treatment growth recovery and catch-up growth in most patients. Clinical trials NCT04775485 (FIREFLY-1); NCT03429803 (PNOC014); NCT05760586 (Expanded Access Program).

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Journal
Neuro-Oncology Pediatrics
Published
2026-04-11
DOI
https://doi.org/10.1093/neuped/wuag021
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

Growth recovery in patients with BRAF -altered pediatric low-grade glioma following treatment with tovorafenib

Daniel Landi, K. Nysom, Pablo Hernáiz Driever, Lindsey Ott et al.
Neuro-Oncology Pediatrics
Glioma Diagnosis and Treatment
article

Growth recovery in patients with BRAF -altered pediatric low-grade glioma following treatment with tovorafenib

Daniel Landi, K. Nysom, Pablo Hernáiz Driever, Lindsey Ott, Lindsay Kilburn, Cassie Kline, Mohamed Shebl Abdelbaki, Karen D. Wright, Soeren Mueller, Jiaheng Qiu, Lisa M. McLeod, Katherine Pehlivan, Dong-Anh Khuong-Quang, Loan Tran, Simon Bailey, A Yin Edwards, Jasper van der Lugt, Sarah E S Leary, Susan N Chi, Elias J Sayour, Olaf Witt, Valerie Larouche
article en

Abstract

Abstract Background The type II RAF inhibitor tovorafenib is US FDA-approved for patients ≥6 months of age with BRAF-altered, relapsed/refractory, pediatric low-grade glioma (pLGG). It is hypothesized that tovorafenib may inhibit CRAF within growth plate chondrocytes, slowing growth plate maturation and linear growth. This analysis investigated growth recovery after treatment with tovorafenib and factors that may impact growth recovery trajectories. Methods This was a retrospective pooled analysis of on- and off-treatment growth in children with BRAF-altered relapsed/refractory pLGG treated with tovorafenib for ≥6 months in two clinical trials and an expanded access program. Patients had to have at least one height measurement recorded &amp;gt;90 days post-treatment as of December 16, 2024. Growth suppression, recovery, and catch-up growth were derived from annualized growth velocity on and off treatment. Exposure–growth models explored growth patterns on and off treatment. Results Sixty-eight patients were included with median (range) baseline age of nine (2-16) years and median follow up 10 months post-treatment. Ninety percent of patients exhibited growth suppression during treatment, of whom 93% showed early post-treatment growth recovery and 77% showed catch-up growth. Reversible growth suppression was observed in both sexes across ages. Of 26 patients with on-treatment bone age, there was no abnormal advancement of bone age on or off treatment. Exposure–growth models suggest that younger baseline age may be associated with faster growth recovery off treatment. Conclusions Growth suppression observed with tovorafenib was reversible, with evidence of post-treatment growth recovery and catch-up growth in most patients. Clinical trials NCT04775485 (FIREFLY-1); NCT03429803 (PNOC014); NCT05760586 (Expanded Access Program).

Neuro-Oncology Pediatrics
Royal Children's Hospital (AU), St. Louis Children's Hospital (US), Children's Hospital of Philadelphia (US), Duke University (US), German Cancer Research Center (DE), University of California, San Francisco (US), Washington University in St. Louis (US), Heidelberg University (DE), University Hospital Heidelberg (DE), Copenhagen University Hospital (DK), Rigshospitalet (DK), University of Florida (US), Humboldt-Universität zu Berlin (DE), Seattle Children's Hospital (US), Center for Cancer and Blood Disorders (US), National Center for Tumor Diseases (DE), Hopp Children's Cancer Center Heidelberg (DE), NGM Biopharmaceuticals (United States) (US), Princess Máxima Center (NL), University Children's Hospital Zurich (CH), Great North Children's Hospital (GB), International Drug Development (FR), Dana-Farber/Boston Children's Cancer and Blood Disorders Center (US), Université Laval (CA)
Openalex Percentile: Top 18%
Glioma Diagnosis and Treatment
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