katero
Jul 01, 2026

Brain cancer breakthrough as new drug shows 'promising results'

A groundbreaking immunotherapy treatment could help push the deadliest form of brain cancer into remission, a study suggests. 

Researchers in London and Canada have found that a new CAR-T cell therapy may eliminate aggressive glioblastoma tumours and lead to long-term disease survival.

It could be a major breakthrough in the fight against the currently incurable cancer, which affects 3,200 Britons per year and devastatingly kills 95 per cent of patients within just five years of diagnosis.

Scientists have spent decades searching for ways to manage glioblastoma but it has proved difficult because the disease spreads through the brain by sending tiny, thread-like extensions into healthy tissue.

Unlike many other cancers, it also cannot typically be fully removed with surgery and remaining cells often resist chemotherapy and radiotherapy, allowing the disease to thrive.

Now, however, teams at King's College London and McMaster University believe CAR-T therapy could be the answer.

Already available on the NHS, CAR-T is used to treat around 2,500 patients in Britain each year - often for blood cancers - and works by instructing a patient's own immune cells to recognise cancer cells in the body and destroy them.

In the new study, published in the journal Nature, scientists tested a new version of the treatment in animals with glioblastoma using models designed to mimic the human disease.

Researchers in London and Canada have found that a new CAR-T cell therapy may eliminate aggressive glioblastoma tumours and lead to long-term disease survival

Researchers in London and Canada have found that a new CAR-T cell therapy may eliminate aggressive glioblastoma tumours and lead to long-term disease survival

Strikingly, in two of the main experiments, the therapy completely eliminated tumours in 12 out of 13 mice treated. 

The mice also remained tumour-free for longer than four months in one group, and for more than five months in another.

The scientists' method involved identifying a protein, named GPNMB, on glioblastoma and macrophages - immune cells that normally help defend the body from infection but are hijacked by cancer to resist treatment.

They then engineered the CAR-T therapy to recognise the protein, allowing them to attack both the tumour and the cells protecting it.

Sheila Singh, professor of neuro-oncology and neurosurgery at King's College London and McMaster University, and the study's lead author, said: 'Instead of treating glioblastoma as only a mass of cancer cells, we need to think of it as a connected tumour-immune ecosystem.

Glioblastoma affects 3,200 Britons per year and kills 95 per cent of patients within just five years of diagnosis. Labour politician Dame Tessa Jowell died from the disease in 2018

Glioblastoma affects 3,200 Britons per year and kills 95 per cent of patients within just five years of diagnosis. Labour politician Dame Tessa Jowell died from the disease in 2018

'Our approach targets both the tumour and the environment that allows it to thrive.

'By going beyond the cancer cells alone, we are also targeting immune cells that help shield the tumour from treatment.'

Although the treatment has not yet been tested on humans, authors say their results demonstrated 'strong preclinical efficacy'. This could open the door for the therapy to one day be used for human treatment if any future trials are successful.

Most glioblastoma patients currently live on average for between 12-18 months, and charity Brain Tumour Research say there have been no advances on a cure for two decades.

CAR-T therapy, meanwhile, is typically used for treating children and adults with leukaemia and for some adults with lymphoma. Both leukaemia and lymphoma are forms of blood cancer.

The process involves collecting white blood cells from a patient's immune system, which the body uses to help fight disease. The cells are then genetically modified to recognise proteins found on cancer cells before being put back into the bloodstream.

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