Nysom Karsten, Kilburn Lindsay B, Leary Sarah E S, Landi Daniel B, de Vos-Kerkhof Evelien, Perreault Sébastien, Witt Olaf, Ziegler David S, Hernáiz Driever Pablo, Franson Andrea T, Baxter Patricia A, Whipple Nicholas S, Kline Cassie, Segal Devorah, Jabado Nada, Bailey Simon, McCowage Geoffrey, Hansford Jordan R, Khuong-Quang Dong-Anh, Gottardo Nicholas G, Hassall Timothy, Han Jung Woo, Yalon Oren Michal, Chi Susan N, Qiu Jiaheng, Da Costa Daniel, Govinda Raju Sandya, Manley Peter, Hargrave Darren
Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Capital Region of Denmark, Denmark.
Children's National Hospital, Washington, District of Columbia, USA.
Neuro Oncol. 2025 Jun 21;27(5):1341-1355. doi: 10.1093/neuonc/noae274.
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.
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.
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.
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.
由于视神经通路胶质瘤(OPG)的解剖位置,手术切除很少能将其治愈。鉴于保留视觉功能的重要性,我们在2期FIREFLY-1试验的OPG亚组中分析了II型RAF抑制剂托法替尼的放射学和视力(VA)结果。
FIREFLY-1研究了托法替尼(420mg/m²,每周一次;最大剂量600mg)在BRAF改变的复发/难治性儿童低级别胶质瘤(pLGG)患者中的疗效(1组,n = 77)、安全性和耐受性(1/2组)。在这项事后分析中,对1组患有OPG的患者的抗肿瘤活性和视力进行了分析。抗肿瘤活性根据神经肿瘤学高级别胶质瘤反应评估(RANO-HGG)、儿科神经肿瘤学-低级别胶质瘤反应评估(RAPNO)和RANO-低级别胶质瘤标准进行独立评估。数据截止日期为2023年6月5日。
77例患者中有42例患有OPG;42例中的35例进行了≥2次视力评估。根据RANO-HGG、RAPNO和RANO-低级别胶质瘤标准,OPG亚组的总体缓解率分别为64%、50%和55%,临床获益率分别为95%、88%和90%。80%的患者个体视力得以保留;31%的患者视力有所改善;87%的患眼视力得以保留,27%的患眼视力有所改善。1组OPG亚组的安全性概况与FIREFLY-1总体安全性分析集相似。
托法替尼在复发/难治性BRAF改变的OPG中,根据放射学评估标准显示出抗肿瘤活性,并且总体耐受性良好。重要的是,大多数患者的视力保持稳定或有所改善。