Patient and caregiver experiences with selumetinib for the treatment of pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas
Julia Meade, Michael Blackowicz, Ayo Adeyemi, Randolph de la Rosa Rodriguez, Xiaoqin Yang, Theresa Dettling

TL;DR
This study explores how pediatric patients with neurofibromatosis type 1 and their caregivers experience treatment with selumetinib for plexiform neurofibromas.
Contribution
It provides novel qualitative insights into patient and caregiver experiences with selumetinib treatment in real-world settings.
Findings
Patients and caregivers reported pain improvement and better quality of life after starting selumetinib.
Caregivers played a central role in treatment decisions and perceived benefits like tumor size reduction.
Patients experienced increased energy and improvements across all quality of life domains.
Abstract
Plexiform neurofibromas (PN) affect 20%–50% of patients with neurofibromatosis type 1 (NF1) and can lead to pain, disfigurement, motor dysfunction, compression of vital structures, and risk of malignant degeneration. Selumetinib was the first pharmacotherapy approved for children aged ≥2 years with symptomatic, inoperable PN in the United States and other countries. This qualitative study was conducted to better understand the drivers for initiating selumetinib and the impact of treatment on quality of life (QoL) from the perspective of pediatric patients with NF1–PN and their caregivers. The study included pediatric patients in the United States (aged 9–18 years) who had been prescribed selumetinib (≥6 months), and their caregivers. Interviews were conducted, and thematic analyses were performed to identify key concepts. A saturation approach established the point at which no new key…
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Taxonomy
TopicsNeurofibromatosis and Schwannoma Cases · Vascular Malformations Diagnosis and Treatment · Meningioma and schwannoma management
