A phase 2 study of trametinib for patients with pediatric glioma or plexiform neurofibroma with refractory tumor and activation of the MAPK/ERK pathway.

Sébastien Perreault(Centre Hospitalier Universitaire Sainte-Justine), Dorsa Sadat Kiaei(Centre Hospitalier Universitaire Sainte-Justine), Mathieu Dehaes(Centre Hospitalier Universitaire Sainte-Justine), Valérie Larouche(Centre hospitalier de l'Université Laval), Uri Tabori(University of Toronto), Cynthia Hawkin(Hospital for Sick Children), Sarah Lippé(Centre Hospitalier Universitaire Sainte-Justine), Benjamin Ellezam(Centre Hospitalier Universitaire Sainte-Justine), Édith Cantin(Université Laval), Marie-Ève Routhier(Université Laval), Maxime Caru(Children's Hospital of Philadelphia), Stéphanie Vairy(Centre Hospitalier Universitaire de Sherbrooke), Geneviève Legault(McGill University Health Centre), Éric Bouffet(University of Toronto), Vijay Ramaswamy(Hospital for Sick Children), Hallie Coltin(Hospital for Sick Children), Lucie Lafay‐Cousin(Alberta Children's Hospital), Juliette Hukin(BC Children's Hospital), Craig Erker(Izaak Walton Killam Health Centre), Nada Jabado(McGill University Health Centre), TRAM-01 Study Team
Journal of Clinical Oncology
June 1, 2022
Cited by 11

Abstract

2042 Background: Pediatric low-grade gliomas (PLGG) are the most frequent brain tumors in children and the majority of PLGG have activation of the MAPK/ERK pathway. Plexiform neurofibromas (PN) are found in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PLGG and PN, but no clinical trial has reported its efficacy. Methods: This multicenter phase II trial includes patients aged ≥ 1 month to ≤ 25 years with progressing/refractory PLGG groups or PN. The primary objective was to evaluate the overall response rate after daily oral trametinib administration for eighteen 28-day cycles. Results: As of January 31 st , 2022, 60 patients with PLGG and 45 patients with PN have been enrolled. Median age is 9.5 years (range 1.8-25.4) for PLGG and 11 years (range 0.7-19.8) for PN. Median follow-up is 18 months (range 0.1-38.1). Fifty-three patients with PLGG were evaluable. The overall response includes: 1 complete response (CR) (1.9%), 7 partial response PR (13.2%), 17 minor response MR (32.1%), 23 stable disease (SD) (43.4%) and 5 progressive disease (PD) (9.4%). Twenty-eight patients with a total of 32 PN were available for volumetric analysis. Volumetric assessment demonstrated an overall response rate of 60.7% compared to 24.1% when using RECIST 1.1 and 62.5% of PN showed a decrease of more than 20% in volume. Median volume change was a decrease of 30% (range -93.5 to 14.3). A total of 59 (69.4%) patients discontinued treatment as planned after 18 cycles and 9 (10.6%) patients had to stop trametinib due to adverse events. Conclusions: Response rates observed in our study suggest that trametinib is a potentially effective targeted therapy for patients with recurrent/refractory PLGG and PN. Treatment was overall well tolerated. This trial will continue to gather data on duration of response and long-term outcome for PLGG and PN treated with trametinib. Clinical trial information: NCT03363217.


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