TY - JOUR
T1 - Radiographic and visual response to the type II RAF inhibitor tovorafenib in children with relapsed/refractory optic pathway glioma in the FIREFLY-1 trial
AU - Nysom, Karsten
AU - Kilburn, Lindsay B
AU - Leary, Sarah E S
AU - Landi, Daniel B
AU - de Vos-Kerkhof, Evelien
AU - Perreault, Sébastien
AU - Witt, Olaf
AU - Ziegler, David S
AU - Hernáiz Driever, Pablo
AU - Franson, Andrea T
AU - Baxter, Patricia A
AU - Whipple, Nicholas S
AU - Kline, Cassie
AU - Segal, Devorah
AU - Jabado, Nada
AU - Bailey, Simon
AU - McCowage, Geoffrey
AU - Hansford, Jordan R
AU - Khuong-Quang, Dong-Anh
AU - Gottardo, Nicholas G
AU - Hassall, Timothy
AU - Han, Jung Woo
AU - Yalon Oren, Michal
AU - Chi, Susan N
AU - Qiu, Jiaheng
AU - Da Costa, Daniel
AU - Govinda Raju, Sandya
AU - Manley, Peter
AU - Hargrave, Darren
N1 - © The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.
PY - 2025/6/21
Y1 - 2025/6/21
N2 - BACKGROUND: Due to their anatomical locations, optic pathway gliomas (OPGs) can rarely be cured by resection. Given the importance of preserving visual function, we analyzed radiological and visual acuity (VA) outcomes for the type II RAF inhibitor tovorafenib in the OPG subgroup of the phase 2 FIREFLY-1 trial.METHODS: FIREFLY-1 investigated the efficacy (arm 1, n = 77), safety, and tolerability (arms 1/2) of tovorafenib (420 mg/m2 once weekly; 600 mg maximum) in patients with BRAF-altered relapsed/refractory pediatric low-grade glioma (pLGG). In this post hoc analysis, anti-tumor activity and VA were analyzed in arm 1 patients with OPG. Anti-tumor activity was independently assessed per Response Assessment in Neuro-Oncology high-grade glioma (RANO-HGG), Response Assessment in Pediatric Neuro-Oncology-LGG (RAPNO), and RANO-LGG criteria. The data cutoff was June 5, 2023.RESULTS: Forty-two of 77 patients had OPGs; 35 of 42 had ≥2 VA assessments. The overall response rate in the OPG subgroup according to RANO-HGG, RAPNO, and RANO-LGG criteria were 64%, 50%, and 55%, with clinical benefit rates of 95%, 88%, and 90%, respectively. VA per patient was preserved for 80% of patients; 31% demonstrated improved VA; VA per eye was preserved in 87%, with 27% improving. The safety profile in the arm 1 OPG subgroup was similar to the overall FIREFLY-1 safety analysis set.CONCLUSIONS: Tovorafenib demonstrated anti-tumor activity in relapsed/refractory BRAF-altered OPG across radiological assessment criteria and was generally well tolerated. Importantly, vision remained stable or improved in most patients.
AB - BACKGROUND: Due to their anatomical locations, optic pathway gliomas (OPGs) can rarely be cured by resection. Given the importance of preserving visual function, we analyzed radiological and visual acuity (VA) outcomes for the type II RAF inhibitor tovorafenib in the OPG subgroup of the phase 2 FIREFLY-1 trial.METHODS: FIREFLY-1 investigated the efficacy (arm 1, n = 77), safety, and tolerability (arms 1/2) of tovorafenib (420 mg/m2 once weekly; 600 mg maximum) in patients with BRAF-altered relapsed/refractory pediatric low-grade glioma (pLGG). In this post hoc analysis, anti-tumor activity and VA were analyzed in arm 1 patients with OPG. Anti-tumor activity was independently assessed per Response Assessment in Neuro-Oncology high-grade glioma (RANO-HGG), Response Assessment in Pediatric Neuro-Oncology-LGG (RAPNO), and RANO-LGG criteria. The data cutoff was June 5, 2023.RESULTS: Forty-two of 77 patients had OPGs; 35 of 42 had ≥2 VA assessments. The overall response rate in the OPG subgroup according to RANO-HGG, RAPNO, and RANO-LGG criteria were 64%, 50%, and 55%, with clinical benefit rates of 95%, 88%, and 90%, respectively. VA per patient was preserved for 80% of patients; 31% demonstrated improved VA; VA per eye was preserved in 87%, with 27% improving. The safety profile in the arm 1 OPG subgroup was similar to the overall FIREFLY-1 safety analysis set.CONCLUSIONS: Tovorafenib demonstrated anti-tumor activity in relapsed/refractory BRAF-altered OPG across radiological assessment criteria and was generally well tolerated. Importantly, vision remained stable or improved in most patients.
KW - Humans
KW - Child
KW - Male
KW - Female
KW - Child, Preschool
KW - Neoplasm Recurrence, Local/drug therapy
KW - Optic Nerve Glioma/drug therapy
KW - Adolescent
KW - Visual Acuity/drug effects
KW - Follow-Up Studies
KW - Proto-Oncogene Proteins B-raf/antagonists & inhibitors
KW - Protein Kinase Inhibitors/therapeutic use
KW - Prognosis
KW - Drug Resistance, Neoplasm
UR - http://www.scopus.com/inward/record.url?scp=105009352825&partnerID=8YFLogxK
U2 - 10.1093/neuonc/noae274
DO - 10.1093/neuonc/noae274
M3 - Journal article
C2 - 39700439
SN - 1522-8517
VL - 27
SP - 1341
EP - 1355
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 5
ER -