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Paediatric high-grade gliomas: Research reveals effective targeting with avapritinib

1 Apr 2025
Paediatric high-grade gliomas: Research reveals effective targeting with avapritinib

Paediatric high-grade gliomas, particularly H3K27M diffuse midline gliomas (DMG), are aggressive malignant brain tumours with a poor prognosis.

Previous research suggests that platelet-derived growth factor receptor alpha (PDGFRA) appears to play a multifaceted role in the pathogenesis of both adult and paediatric high-grade gliomas.

Not only are genetic alterations of PDGFRA common in patients with paediatric high-grade gliomas, but elevated PDGFRA expression has been shown to be key in driving growth of DMG tumours.

Now, findings of a recent multicenter study led by Mariella Filbin, MD, PhD, co-director of the Brain Tumour Centre at Boston Children’s Hospital and Dana-Farber Cancer Institute, suggest that PDGFRA could be a potential therapeutic target for paediatric high-grade gliomas.

Filbin and her team — including collaborators at the University of Michigan Medical School and the Medical University of Vienna — also provide the first real-world clinical data to support the use of a PDGFRA inhibitor in the treatment of certain paediatric patients with high-grade gliomas.

To determine the frequency of PDGFRA alterations in paediatric high-grade gliomas, Filbin and her colleagues analysed genomic data from 217 paediatric high-grade glioma samples.

They identified PDGFRA alterations in nearly 15 percent of patients.

Using transcriptomic data, they also found significantly elevated PDGFRA expression in tumours with PDGFRA mutation or amplification.

Next, the team tested the activity of four PDGFRA inhibitors (dasatinib, crenolanib, axitinib, and avapritinib) against a panel of glioma cell lines with PDGFRA alterations.

Of these drugs, avapritinib exhibited the highest potency.

Additional pre-clinical testing found that avapritinib also had the least amount of off-target kinase activity, suggesting drug is less likely to cause unintended side effects.

Finally, following additional testing in mouse models, the researchers treated eight paediatric and young adult patients who had high-grade gliomas with avapritinib through a compassionate use programme.

Most of the patients had DMGs, and seven of the eight had PDGFRA alterations.

All had previously undergone surgical biopsy or resection and radiation, and four had also received chemotherapy or other treatment approaches.

After being treated with avapritinib once daily for an average of four months, three of the patients demonstrated a radiographic response.

The drug was also well tolerated.

These three patients also survived roughly twice as long as those who didn’t respond to avapritinib, although their disease ultimately metastasised.

This early data suggests that avapritinib is generally safe and may trigger an initial clinical response in a small group of patients who have paediatric high-grade gliomas with PDGFRA amplification.

“Our research now provides the basis for a clinical trial for avapritinib in newly diagnosed paediatric patients,” says Filbin.

“Our follow-up work focuses on genetic markers for personalised treatment and developing combination therapies with FDA-approved drugs to enhance efficacy.”

Source: Boston Children's Hospital