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Brain Cancer in Infants Could Be Treated With Targeted Drugs

Brain Cancer in Infants Could Be Treated With Targeted Drugs

Brain Cancer in Infants Could Be Treated With Targeted Drugs

Brain Cancer in Infants Could Be Treated With Targeted Drugs

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Brain cancer in infants is biologically distinct from other childhood brain tumors and could be successfully treated with targeted drugs, a new study has shown.

An aggressive type of brain tumor, called high-grade glioma, is almost always fatal in older children – with only 20 per cent surviving for more than five years.

Babies and very young children, diagnosed when they are less than 12 months old, tend to have a better outcome – with around two thirds surviving five years or more.

In the largest and most comprehensive study of infant gliomas to date, scientists found that these tumors are molecularly different from those in older children, helping explain why they tend to be less aggressive.

The new results could help pick out babies with brain tumors who could be spared chemotherapy – which can have devastating side-effects and be particularly harmful while their brain is still developing.

The study found that brain tumors in babies often had specific molecular weaknesses which could be targeted by existing targeted drugs – and clinical trials to assess these are now set to open.

Entirely different genetic make-up

Scientists at The Institute of Cancer Research, London, carried out a large-scale study of 241 infants from around the world diagnosed with glioma brain tumors – working with colleagues at the Hopp Children’s Cancer Center Heidelberg in Germany, the UCL Great Ormond Street Institute of Child Health, and St. Jude Children’s Research Hospital in the US.

The researchers found that 130 of the 241 tumor samples – or 54 per cent – had an entirely different genetic make-up from other forms of childhood brain tumors, despite looking highly similar under the microscope.

Some 65 cases, or half of children with the distinct form of infant brain tumors, had specific molecular weaknesses – including ALK and NTRK gene fusions, which can be targeted with existing precision medicines.

The study is published in Cancer Discovery today (Thursday), and was funded by charities including the CRIS Cancer FoundationThe Brain Tumour CharityChildren with Cancer UKGreat Ormond Street Hospital Children's CharityCancer Research UK and ALSAC, the fundraising and awareness organisation of St. Jude.

Targeted treatment significantly shrunk tumours

Next, the team looked at mice with brain tumors caused by ALK gene fusions to compare the effect of a targeted drug, lorlatinib, which works by blocking ALK, with temozolomide chemotherapy.

They found that lorlatinib significantly shrunk tumours in seven out of eight mice, or 88 per cent, while tumors in mice given chemotherapy kept growing, though at a slower rate.

The researchers also grew three-dimensional ‘mini tumors’ in the lab from patient samples, and found those that had fusions of NTRK with other genes were particularly sensitive to drugs blocking NTRK.

Tumors with these fusion mutations were between two and nine times more sensitive to the targeted treatments entrectinib, crizotinib and milciclib than those without.

A small number of children whose tumors were analysed in the study were successfully treated with ALK or NTRK targeting drugs, offering further evidence for the promise of targeted treatments for infant brain tumors.

Testing the benefit of targeted drugs in clinical trials

Clinical trials are due to open to test the benefit of targeted drugs blocking the ALK and NTRK gene fusions in infant brain tumors – and to better understand the biology of tumors which don’t have these faults.

The new results are also set to change the World Health Organization’s diagnostic guidelines, with brain tumours in infants to be classed separately from other childhood brain tumors.

Professor Chris Jones, Professor of Paediatric Brain Tumor Biology at The Institute of Cancer Research, London, said:

“We found that glioma brain tumors in babies are biologically completely different to those in older children, even though under the microscope they look much the same.

“Our study offers the biological evidence to pick out those infants who are likely to have a better outcome from their disease, so these very small children and their families can be spared the harmful effects of chemotherapy.

“We showed that brain tumors in infants have particular genetic weaknesses that could be targeted with existing drugs – and clinical trials are planned to test the benefit of these precision medicines as a first-line treatment as soon as possible.”

‘Some children could be spared chemotherapy’

Dr Matthew Clarke, Clinical Research Fellow in the Glioma Team at The Institute of Cancer Research, London, said:

“Brain tumors that arise in the very youngest children tend to have better outcomes from those in older children – and our new study explains that difference on a biological level.

“Chemotherapy is currently a good treatment option for babies with brain tumors – but our study has found that some children could be spared this treatment. With further testing, I’m hopeful that existing targeted drugs could expand our arsenal of options to treat these smallest of patients.”

Professor Paul Workman, Chief Executive of The Institute of Cancer Research, London, said:

“It’s especially cruel when cancer affects such small children, so it is encouraging that this study offers some hope for very young patients and their families.

“The research offers a better understanding of the biology of brain tumors in infants, and finds that they might potentially be treated with new targeted drugs.

“That’s vitally important because infants are particularly vulnerable to the side effects from standard treatments such as chemotherapy, and we need much better, kinder options.”

Reference: Clarke, et al. (2020) Infant high grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes. Cancer Discovery DOI: 10.1158/2159-8290.CD-19-1030

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