# Patient and caregiver experiences with selumetinib for the treatment of pediatric patients with neurofibromatosis type 1 and plexiform neurofibromas

**Authors:** Julia Meade, Michael Blackowicz, Ayo Adeyemi, Randolph de la Rosa Rodriguez, Xiaoqin Yang, Theresa Dettling

PMC · DOI: 10.1093/nop/npaf078 · 2025-08-05

## 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.

## Key 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 concepts were being identified with successive interviews.

Prior to initiating selumetinib, children (N = 10) and their caregivers (N = 19) reported that PN-related issues, such as pain, impacted the lives of those with NF1–PN. Caregivers played a key role in treatment decisions, and initiation of selumetinib helped meet treatment goals, including PN size reduction, pain improvement, and improved QoL. Patients experienced increased energy, and improvements in pain and all QoL domains post-selumetinib initiation.

Overall, patients and caregivers reported improvements in pain and QoL after selumetinib initiation. The qualitative, real-world nature of this study provides insights into patient and caregiver perspectives, and the impact of selumetinib on the patient journey.

## Linked entities

- **Chemicals:** selumetinib (PubChem CID 10127622)
- **Diseases:** neurofibromatosis type 1 (MONDO:0018975)

## Full-text entities

- **Genes:** NF1 (neurofibromin 1) [NCBI Gene 4763] {aka NFNS, VRNF, WSS}
- **Diseases:** genetic disorder (MESH:D030342), motor dysfunction (MESH:D000068079), neurofibromas (MESH:D009455), disabilities (MESH:D009069), nerve sheath tumors (MESH:D018317), fibromas (MESH:D005350), confusion (MESH:D003221), PN (MESH:D018318), exhaustion (MESH:D006359), learning limitations (MESH:D007859), ADHD (MESH:D001289), cancer (MESH:D009369), irritation (MESH:D001523), blood loss (MESH:D016063), compression (MESH:D009408), nerve damage (MESH:D000080902), Pain (MESH:D010146), Rare Disease (MESH:D035583)
- **Chemicals:** ARRY-142886 (MESH:C517975)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12965642/full.md

---
Source: https://tomesphere.com/paper/PMC12965642