4.1 Article

Trametinib for orbital plexiform neurofibromas in young children with neurofibromatosis type 1

Journal

CHILDS NERVOUS SYSTEM
Volume 37, Issue 6, Pages 1909-1915

Publisher

SPRINGER
DOI: 10.1007/s00381-021-05127-6

Keywords

Orbitofacial; Plexiform neurofibroma; Neurofibromatosis type 1; Trametinib

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Trametinib can reduce tumor size in some young children with orbital PNF and may prevent progressive disfigurement. The dosages are adjusted for children of different ages, with no changes in visual function observed during treatment, but some children experienced skin and nail toxicities of grades 1-2.
Introduction Plexiform neurofibromas (PNF) in neurofibromatosis type 1 (NF1) are usually diagnosed in childhood and can grow rapidly during this period. In 10% of patients, PNF involve the orbital-periorbital area and may cause visual problems including glaucoma, visual loss from amblyopia (deprivational, strabismic, or refractive), optic nerve compression, or keratopathy. Ptosis, proptosis, and facial disfigurement lead to social problems and decreased self-esteem. Complete surgical removal involves significant risks and mutilation, and regrowth after debulking is not uncommon. Inhibitors of the RAS/MAPK pathway have recently been investigated for their activity in PNF. We administered the oral MEK inhibitor trametinib to five young children with NF1 and PNF of the orbital area, with visual compromise and progressive tumor growth; and followed them clinically and by volumetric MRI. Methods Treatment was initiated at a mean age of 26.8 months (SD +/- 12.8) and continued for a median 28 months (range 16-51). Doses were 0.025 mg/kg/day for children aged > 6 years and 0.032 mg/kg/day for those aged < 6 years. Results Volumetric MRI measurements showed a reduction of 2.9-33% at 1 year after treatment initiation, with maximal reductions of 44% and 49% in two patients, at 44 and 36 months, respectively. No change in visual function was recorded during treatment. One child reported decreased orbital pain after 2 weeks; and another, with involvement of the masseters, had increased ability to chew food. Toxicities were mostly to skin and nails, grades 1-2. Conclusions Trametinib can decrease tumor size in some young children with orbital PNF and may prevent progressive disfigurement.

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