CTP-17. Clinical stability following tovorafenib treatment in relapsed/refractory pediatric low-grade glioma: updated results from the phase 2 FIREFLY-1 trial
Abstract BACKGROUND Tovorafenib is a selective, CNS-penetrant, type II RAF inhibitor that is FDA approved for recurrent BRAF-altered pLGG based on results of the ongoing FIREFLY-1 (NCT04775485) phase 2 study. METHODS 77 patients enrolled in the registrational arm (Arm 1) of FIREFLY-1. After 26 or more cycles (28 days each), patients could stop tovorafenib (drug holiday) and reinitiate upon radiographic or clinical evidence of progressive disease (PD). RESULTS As of May 10, 2024 data cutoff, objective response rate (ORR; RAPNO) for arm 1 (n=77) was 53%; median duration of response (DOR) was 18 months (range 12.0-22.8). 44 patients completed a 26-cycle course; 33/44 (75%) patients opted to enter drug holiday per protocol, with median follow-up since last dose of 4.4 months (range 0.2-11.6). 15/33 (45%) did not have radiographic PD prior to treatment cessation; PD events occurred in 5/15 patients by 6 months post treatment cessation. A more recent data extract (May 21, 2025) showed 5 additional patients entered drug holiday (n=38); median follow-up since last dose was 15.6 months (range 1.4-24.0). 30/38 (79%) remained clinically stable irrespective of radiographic response, with 28 (74%) remaining without retreatment ≥12 months from last dose. 2 patients exited study early, 7.7 months and 3 months from last dose. 8/38 (21%) were retreated with tovorafenib and remained on retreatment at time of extract. No new toxicities were reported with retreatment. Updated data from a prespecified data cut with approximately 36-month follow-up will be presented, including DOR, time to next treatment with ≥12 months off tovorafenib, and activity of tovorafenib at retreatment. CONCLUSIONS Tovorafenib induces durable responses with evidence of clinical stability off treatment in patients with recurrent BRAF-altered pLGG. Progression can occur after cessation, but retreatment is feasible.
Authors
- Daniel Landi (ORCID: https://orcid.org/0000-0002-1487-1136)
- Darren Hargrave (ORCID: https://orcid.org/0000-0001-8219-9807)
- Angela J. Waanders (ORCID: https://orcid.org/0000-0002-0571-2889)
- Peter Manley (ORCID: https://orcid.org/0000-0003-3485-4517)
- Sarah Leary (ORCID: https://orcid.org/0000-0003-0225-6184)
- Elly Barry (ORCID: https://orcid.org/0000-0002-6890-2444)
- Lindsay Kilburn (ORCID: https://orcid.org/0000-0003-1478-3619)
- David S. Ziegler (ORCID: https://orcid.org/0000-0001-7451-7916)
- Jingyang Zhang (ORCID: https://orcid.org/0000-0002-4347-9416)
- Cassie Kline (ORCID: https://orcid.org/0000-0001-7765-7690)
- Jasper van der Lugt (ORCID: https://orcid.org/0000-0002-8186-338X)
- Karsten Nysom (ORCID: https://orcid.org/0000-0003-2935-0058)
- Sébastien Perreault (ORCID: https://orcid.org/0000-0002-4417-7698)
- Sabine Mueller (ORCID: https://orcid.org/0000-0002-8216-9357)
- Olaf Witt
- Dong-Anh Khong-Quang
Institutions
- Royal Children's Hospital (AU)
- Children's Hospital of Philadelphia (US)
- Children's National (US)
- Duke University (US)
- University of California, San Francisco (US)
- Great Ormond Street Hospital (GB)
- Centre Hospitalier Universitaire Sainte-Justine (CA)
- Copenhagen University Hospital (DK)
- Rigshospitalet (DK)
- Center for Cancer and Blood Disorders (US)
- Hopp Children's Cancer Center Heidelberg (DE)
- NGM Biopharmaceuticals (United States) (US)
- Sydney Children's Hospital (AU)
- Lurie Children's Hospital (US)
- Princess Máxima Center (NL)
- University College London (GB)
- Université de Montréal (CA)
Publication Details
- Journal
- Neuro-Oncology
- Published
- 2025-11-01
- DOI
- https://doi.org/10.1093/neuonc/noaf201.0589
- Primary Topic
- Melanoma and MAPK Pathways
- Type
- article
- Field-Weighted Citation Impact
- 0.00