Brain tumour research
This page is about research into the causes, prevention and treatments of brain tumours. You can find the following information
- A quick guide to what's on this page
- Why we need research
- Clinical trials
- Causes of brain tumours
- Diagnosing brain tumours
- Research into surgery for brain tumours
- Radiotherapy research for brain tumours
- Chemotherapy research for brain tumours
Brain tumour research
All treatments must be fully researched before they can be adopted as standard treatment for everyone. This is so that we can be sure they work better than the treatments we already use. And so we know that they are safe.
First of all, treatments are developed and tested in laboratories. Only after we know that they are likely to be safe to test are they tested in people, in clinical trials. Cancer Research UK supports a lot of UK laboratory research into cancer and also supports many clinical trials.
There is research into the causes and diagnosis of brain tumours. There is a lot of research into treatment for brain tumours, including into treating children.
All treatments have to be fully researched before they can be adopted as standard treatment for everyone. This is so that
- We can be sure they work
- We can be sure they work better than the treatments that are available at the moment
- They are known to be safe
First of all, treatments are developed and tested in laboratories. For ethical and safety reasons, experimental treatments must be tested in the laboratory before they can be tried in patients. If a treatment described here is said to be at the laboratory stage of research, it is not ready for patients and is not available either within or outside the NHS. Cancer Research UK supports a lot of UK laboratory research into cancer.
Tests in patients are called clinical trials. Caner Research UK supports many UK and international clinical trials.The trials and research section has information about what trials are including information about the 4 phases of clinical trials. If you are interested in taking part in a clinical trial, go to our searchable database of clinical trials. If there is a trial you are interested in, print it off and take it to your own specialist. If the trial is suitable for you, your doctor will need to make the referral to the research team.
All the new approaches covered here are the subject of ongoing research. Until studies are completed and new effective treatments are found, these treatments cannot be used as standard therapy for brain tumours.
Cancer Research UK scientists are looking into the differences between the genes in brain tumour cells and normal cells. They have already found some common gene faults and are hoping that investigating these will lead to new ways of diagnosing and treating brain tumours.
The National Brain Tumour Study is looking at blood samples from people who have had a brain tumour in the last 5 years to find out more about the genetic causes of brain tumours. They are also looking into how doctors in the future may be able to use the gene changes to tailor treatment to individual patients.
There is a study looking at gene changes in pituitary tumours. The UK CYAB study is a small study of children and young people up to 24 years old, looking at factors such as diet, lifestyle, and history of infections, to try to find what might cause brain tumours in this age group.
You can find out more about these trials on our clinical trials database. Choose 'brain tumours' from the dropdown list of cancer types.
Research is looking into improving scans and diagnosis. These include some new types of scan.
One recent trial tested a new type of MRI scan called DTI (Diffusor Tension Imaging). It is also sometimes called tractography. Standard MRI can’t show up important bundles of white nerve fibres. Damage to these white nerve bundles during surgery can have serious effects. Surgeons have to find out where these nerves are and if they are surrounded by the tumour. They can then avoid cutting through the nerve bundles.
The research team found that DTI scans are useful for getting a more detailed picture of the brain than other types of scan. They also found that they could see the difference between nerve bundles, normal tissue and areas of tumour more clearly. The researchers say that it is early days for this new technique, but it may be useful for planning treatment in the future.
The only sure way to diagnose many brain tumours is to have a biopsy done. Looking at the cells under a microscope is the only guaranteed way to identify the type and grade of the tumour. The CNS 2004 10 trial and the CNS 2004 11 trial are looking at a newer less invasive technique to help diagnose brain tumours. It is a type of scan called magnetic resonance spectroscopy (MRS) and doesn’t involve having an operation. MRS is a procedure similar to an MRI scan. But as well as giving a picture of the tumour, MRS also gives doctors information about the activity of the brain tissue.
With information from MRS doctors are able to identify the type and grade of a brain tumour. It also helps them to tell the difference between a brain tumour and other brain disorders such as epilepsy and infections. The use of MRS for diagnosis is still very experimental. We need a lot more research before we will know exactly how reliable and accurate this procedure is. Until we have this, biopsy is still the best method of diagnosing a brain tumour. The UK trials aim to find out if MRS can help in the diagnosis and management of teenagers and children with brain tumours or brain stem tumours.
The advanced MRI scan trial is looking at whether specialised MRI scans can help to decide how and when to treat brain tumours. The new types of MRI scan give information about the size and shape of the tumour. They also show up the blood flow in the brain as well as which chemicals are in the brain, and how they move around.
The above trials are listed on our clinical trials database. To find them, go to the trials database search page and type in 'scans' in the free text search box.
The GALA 5 trial is looking at 2 treatments for glioblastoma. The first treatment is 5-ALA or Gliolan. It is a dye that makes brain tumour cells glow red under ultra violet light. During surgery, it can help surgeons to check they are removing as much brain tumour as possible. The second part of the treatment is a chemotherapy implant called a Gliadel wafer that the surgeon puts into the area of the brain tumour. The aim of this treatment is to kill any tumour cells left after surgery.
The researchers want to see if it is safe to have 5-ALA and Gliadel wafers with standard brain tumour treatments. They also want to find out how many people are helped by this treatment and whether it has an effect on other treatments they have.
Treatment for low grade brain tumours can be challenging for doctors as the tumours can be present for years without causing symptoms. Some doctors prefer to closely monitor the tumours and offer surgery if the tumour grows or becomes more aggressive (watch and wait approach). But other doctors prefer to do surgery to remove the tumour early on, if possible.
A Norwegian study in 2012 compared the different ways of treating low grade gliomas at 2 hospitals. One hospital usually offered people with low grade gliomas surgery early on, whereas doctors at the other hospital preferred to monitor the tumours. Patients at the hospital that usually carried out early surgery lived longer than at the hospital that usually monitored tumours. Further follow up of these patients, and other studies, are needed to confirm these results and help doctors decide on the best treatment for some people with low grade brain tumours.
Researchers are looking into the following
- Stereotactic radiotherapy and radiosurgery
- Boron neutron capture therapy (BCNT)
- Proton therapy
- Hyperfractionated radiotherapy
- Side effects of radiotherapy
The radiotherapy trials mentioned here are listed on our searchable clinical trials database. Choose 'brain tumours' from the dropdown menu of cancer types. You will need to tick the boxes if you want to see the trials that have finished recruiting or that have results. Many of the trials are supported by Cancer Research UK.
Stereotactic radiotherapy is a technique that gives very accurate and high doses of radiation directly into the centre of the brain tumour without damaging the normal surrounding brain tissue. A variation on this is called radiosurgery, which is a single, highly targeted dose of stereotactic radiotherapy. There is detailed information about stereotactic radiotherapy and radiosurgery in this section of the website.
Both stereotactic radiotherapy and radiosurgery are still being researched to find out exactly which tumours they can treat. They are mainly used for brain tumours that have come back or for other cancers that have spread to the brain. They are used for some non cancerous (benign) tumours of the brain, such as acoustic neuroma.
This type of treatment is only suitable for a small number of brain tumours and for particular circumstances. It is less likely to be suitable for larger tumours or for widespread tumours. A number of clinical trials are in progress in the USA and other parts of the world. When the results from these are available, specialists will know more about which tumours these treatments can help.
BCNT is an experimental way of giving radiotherapy. It has been tried in trials with glioblastoma multiforme (grade 4 glioma) and has been used widely in Japan. There are concerns about the levels of side effects of the treatment, so more research is being done in Europe, Japan and the USA. The researchers are looking into using this treatment after surgery to try to reduce the risk of the brain tumours coming back. With BNCT, you have boron injections and external radiotherapy with low energy neutrons. The boron collects in the brain tumour cells and gives off radiation when the neutrons hit.
One of the newer ways of giving radiotherapy uses a different type of beam called a proton beam. Protons collect energy as they slow down and travel through the body. They then release this energy at their target point – the tumour. This means they give a very high dose of radiation to the cancer, but only a low dose to the area around it. So there is less likelihood of damage to nearby healthy tissue.
Proton beam radiotherapy machines in the UK are only able to treat cancer of the eye. The machines are not able to treat cancers deeper in the body. Some countries in Europe and the USA are testing and using proton beam radiation for deeper cancers, including a tumour called chordoma that can occur in the spinal cord or the brain stem. At the moment, if this treatment is suitable for you the NHS pays to send you for treatment abroad – usually to the USA.
The HIT - SIOP PNET 4 trial compared hyperfractionated radiotherapy (with 2 treatments a day) to standard radiotherapy (one treatment a day). It recruited children and young people from the age of 4 to 21 with medulloblastoma. The trial team found that HFRT was no better than standard radiotherapy as part of treatment for medulloblastoma. The researchers also found no significant difference between the side effects of the two treatments.
Radiotherapy treatment is planned very carefully and techniques such as intensity modulated radiotherapy (IMRT) can shape radiation beams to treat the cancer, while avoiding healthy tissue. Although this makes it very precise, radiotherapy can still cause damage to some healthy tissue. The VoxTox study is looking at the side effects of radiotherapy for cancers of the central nervous system and some other types of cancer. The researchers want to understand more about the side effects and to work out how much radiation has reached healthy tissue. The information the researchers collect may help to reduce side effects for people having treatment in the future.
There are always clinical trials testing new combinations or single chemotherapy drugs for brain tumours. Trials also look at drug doses and the order in which you have them (the sequence). Current research is looking at
- Chemotherapy in young people with gliomas
- Chemotherapy for primary lymphoma of the central nervous system (CNS)
Many of the chemotherapy trials are listed on our clinical trials database. To find them, go to the trials database search page and choose ‘brain tumours’ from the dropdown menu of cancer types.
The BR14 trial is looking at radiotherapy with and without temozolomide for anaplastic glioma. Anaplastic means that the cancer cells look less like normal glial cells than other gliomas. Anaplastic cancers often grow more quickly than other cancers. In this trial, some people won’t have temozolomide. Some will have temozolomide during radiotherapy and some will have it after radiotherapy. Some will have it both during and after radiotherapy.
Some people with a brain tumour have changes in two chromosomes called 1p and 19q in the cell. One or both must be normal in everyone taking part in this trial. Doctors call this non 1p19q deleted anaplastic glioma.The aims of this trial are to find out if temozolomide during radiotherapy, after radiotherapy, or during and after radiotherapy is better than radiotherapy alone. And they want to learn more about the side effects.
So far, most of the later stage research into chemotherapy and brain tumours has been for the more aggressive types of brain tumour, such as glioblastoma. The SIOP - LGG 2004 CNS 2004 03 trial is looking at giving etoposide in addition to standard chemotherapy for low grade gliomas in children and teenagers. The trial is also testing giving the chemotherapy for longer than a year to see if this will help stop the tumour regrowing.
The SIOP 99 trial is trying to find out if cyclophosphamide, vincristine and etoposide chemotherapy helps children and young people with ependymoma when it is given with radiotherapy after surgery. The CNS 2001 06 trial is trying to find out whether adding vincristine chemotherapy to radiotherapy works better than radiotherapy alone for young people aged 4 to 21 with medulloblastoma.
Primary CNS lymphoma is a very rare form of non Hodgkin lymphoma which usually only affects the brain. The first treatment for it is usually the chemotherapy drug methotrexate. Doctors think higher doses of methotrexate would work better, but it has serious side effects, including kidney damage and a reduction in blood cell counts. A drug called glucarpidase helps your body to break down methotrexate quickly and get rid of it.
Doctors hope that glucarpidase will protect people from the worst of the side effects of methotrexate, and allow them to give higher doses to fight the lymphoma. A small trial of this treatment is looking to see how safe it is to give higher doses of methotrexate with glucarpidase, and what the side effects will be.
Biological therapies are treatments that use natural substances from the body, or drugs made from these substances to treat cancer. Research is looking into
- Cancer growth blockers
- PARP inhibitors
- Blood supply and brain cancer
- Monoclonal antibodies
- Gene therapy
Some biological therapy drugs called tyrosine kinase inhibitors (TKIs) block signals that tell cancer cells to divide and grow. Imatinib (Glivec) is a TKI drug that works well in treating a type of cancer called gastro intestinal stromal tumour (GIST). Researchers have tried this drug for glioma brain tumours. But the results so far have been mixed, and further trials are needed to see if imatinib is helpful for brain tumours.
Another TKI drug being tested is erlotinib (Tarceva). The Phase 1 NAG 2005 09 trial is looking at how well this might work for children whose brain tumours have continued to grow or have come back after treatment, and for children newly diagnosed with brain stem gliomas, which are very difficult to treat.
The DORIC trial is comparing a combination of cediranib and gefitinib (Iressa) with cediranib alone in people who have glioblastoma that has come back after treatment. Cediranib is a type of biological therapy that stops the cancer growing new blood vessels (see the section on blood supply and brain cancer below). Gefitinib is a tyrosine kinase inhibitor. The aim of this trial is to find out if the combination of cediranib and gefitinib works better than cediranib alone for glioblastoma that has come back after treatment.
PARP is an enzyme that helps damaged cells to repair themselves. If PARP is blocked, cancer cells may not be able to repair themselves after chemotherapy. This could make chemotherapy work better. Olaparib is a PARP inhibitor being looked at in early studies for different types of cancer, including glioblastoma.
There is a phase 1 trial looking at olaparib with temozolamide for glioblastoma that has come back after treatment. The first aim of the trial is to see if olaparib is able to cross the protective blood brain barrier. If it does, then the researchers hope to find the best safe dose of olaparib to have with temozolamide. And to learn more about the side effects of having both drugs together.
Angiogenesis means growth of new blood vessels. A cancer needs to grow its own blood vessels as it gets bigger. Without its own blood supply, it can't continue to grow. Anti angiogenic drugs stop tumours from developing their own blood vessels. This then deprives the cancer of the oxygen and food that it needs. Research using these drugs is ongoing for brain cancers. The drug being tried most in trials for brain cancer is thalidomide. Thalidomide hit the headlines in the 1960s when it was discovered that it caused birth defects by reducing the blood flow to developing limbs in babies in the womb. Since then it has been given to many people with cancer, without causing serious side effects. It is still important not to take this drug if there is any possibility you could be pregnant. Early studies show some promise for treating people with high grade gliomas. But we will need a lot more research to develop this further as a treatment.
The phase 1 EORTC 26054 trial looked at temozolomide with an anti angiogenic drug called enzastaurin, for people with advanced glioma, or newly diagnosed glioma that could not be treated with radiotherapy. The trial recruited 28 people in total. The trial team found that temozolomide and enzastaurin was a safe combination. The trial was too small to draw any firm conclusions about how well the treatment works but the researchers felt it could be a useful combination to treat glioma. But further trials are needed.
Many different monoclonal antibodies (MABs) are being investigated for cancer treatment. MABs are proteins, made in the laboratory from a single copy of a human antibody. When these laboratory made antibodies are injected into patients they seek out cancer cells which carry abnormal proteins.
Researchers are looking at a MAB called bevacizumab (Avastin) for high grade gliomas. There have been studies looking at it on its own, and in combination with chemotherapy or radiotherapy for glioblastoma that has come back. Results so far have been promising. Some researchers are now starting to look at bevacizumab after surgery for people with newly diagnosed glioblastoma. The HERBY trial is looking at adding bevacizumab to radiotherapy and chemotherapy after surgery for children with a high grade glioma.
Researchers are also looking to see if bevacizumab is helpful in treating grade 2 and 3 gliomas. The TAVAREC trial is comparing temozolomide and bevacizumab with temozolomide alone in people with grade 2 or 3 glioma that has come back after treatment.
A number of new gene therapy treatments are being researched. Some doctors and researchers are now using the term molecular therapy which is a more general term. It can include research into
By studying how changes in these genes cause normal cells in the brain to become cancerous, scientists aim to eventually develop gene therapy where damaged genes in the cancer cells can be replaced with normal ones.
Doctors have started to look into a gene therapy called cerepro. One trial used a variation of the herpes simplex virus to deliver gene therapy to people with high grade glioma that has come back or started to grow again since treatment. Another trial has looked at using cerepro after surgery. There are no trials looking at cerepro at the moment. But the company that make it hope to continue with further research in the future.
A phase 1 trial is testing a vaccine for glioblastoma. This trial is looking at a new vaccine called IMA950 for people who have just been diagnosed with a glioblastoma brain tumour. This is an experimental treatment that helps the immune system to kill cancer cells. Researchers are giving it alongside standard treatment of surgery and radiotherapy. People taking part in the trial also have a drug called GM-CSF which helps to stimulate the immune system. Doctors hope this will make the vaccine work better.
A phase 3 trial called ACT IV is looking at a vaccine called rindopepimut for people with glioblastoma. Between a quarter and a third of all glioblastomas may contain a protein called EGFRvIII. Researchers want to see if rindopepimut can train the immune system to recognise this protein and kill the glioblastoma cells. The people taking part have this vaccine alongside temozolomide. The researchers want to find out if rindopepimut helps to shrink glioblastoma or delays it starting to grow again, how it affects the immune system, and to learn more about the side effects and how it affects peoples' quality of life.
An early trial is looking at a vaccine to treat children with high grade glioma. The trial is looking at making personalised vaccines to see if they can stimulate the immune system to kill brain tumour cells. The researchers will make each vaccine using white blood cells called dentritic cells. They mix these with proteins taken from the brain tumour during surgery. The researchers want to see how possible it is to make and give these vaccines to children, to learn more about the safety of vaccines and to see if adding this vaccine to standard treatment helps stimulate the immune system.
Another trial is looking at a personalised vaccine called DCVax-L for glioblastoma multiforme in adults. The dendritic cells are mixed with proteins taken from your brain tumour to make the dendritic cell vaccine. It works by helping your immune system recognise and kill cancer cells.
If you would like to look for current brain tumour trials, you can look on our clinical trials database and choose ‘brain tumour’ from the dropdown menu of cancer types.
Reolysin is a cancer treatment made from a type of virus called reovirus. Reovirus is common and causes only minor symptoms such as coughs, colds and diarrhoea. We know from research that Reolysin kills cancer cells. But we do not yet know if it can reach, or affect, cancer cells in the brain. The REO 13 BRAIN study is an early study looking at giving Reolysin before surgery for people with a primary brain tumour that has come back or who have cancer that has spread to the brain (secondary brain tumour). The researchers will look at the brain tumour tissue removed during surgery to see if the reovirus has affected the cancer cells. They will also monitor how your immune system responds to the virus.
Clomipramine is a drug used for depression, called a tricyclic anti depressant. Some researchers think it might help to treat glioma brain tumours. There has been some lab based research that showed the drug could encourage death of cancer cells, but not healthy brain cells. The researchers say this is encouraging.
A lot more research is needed before we know whether clomipramine can help to treat people with gliomas. There have been no trials reported using clomipramine in people with brain tumours and we are not aware of any trials currently recruiting patients.
Tamoxifen is a type of hormone therapy. This drug is most often used to treat or prevent breast cancer. But it has also been tried for other cancers, including brain tumours. How it works on brain tumours is complex. One theory is that because this drug helps to protect against spread of the cancer to the brain for women with breast cancer, it will have a similar protective effect on people with certain types of brain tumours. Much higher doses are needed for people with brain tumours than for women with breast cancer.
Researchers think that they need to get a large amount of tamoxifen into the brain in a short time. So they are investigating starting with small doses and increasing the dose fairly quickly. We still don’t know whether people should remain on these high doses or if they should have a lower maintenance dose. We also don’t know how long people with a brain tumour would need to carry on taking tamoxifen.
Generally, tamoxifen has few side effects, although it may have more in the high doses used for brain tumours. It can increase the risk of blood clots and people with brain tumours also have a higher risk of blood clots. So it needs to be used with care. There is some evidence to suggest that it should not be taken with the anti epileptic drug called phenytoin. Results from early clinical trials have shown that tamoxifen does not help everyone with a brain tumour but it may help a few. We’ll need larger clinical trials before we will know whether it can help to treat brain tumours.
Photodynamic therapy (PDT) is a type of treatment that makes cells light sensitive and then shines a very bright light onto them. The National Institute for Health and Care Excellence (NICE) has said that there is not yet enough evidence to recommend this as a standard treatment for brain tumours but it can be used as part of clinical trials.
PDT has been tried for brain tumours that have come back after standard treatment. But a recent trial looked at PDT for newly diagnosed brain tumours. The people taking part in this trial had glioblastoma multiforme and had either surgery and radiotherapy, or surgery, PDT and radiotherapy. The researchers found that it took longer for the brain tumours to start growing again in people who had the PDT. In this group of patients, the researchers also found there was more of an improvement in how well they were and how many activities they were able to carry out 6 months after treatment. This was only a small trial of 27 people, and so the researchers suggest this treatment should be looked at in larger trials.
Another trial is comparing different laser wave lengths in PDT for the most common types of brain tumour (glioblastoma multiforme or anaplastic astrocytoma). This trial is looking at giving PDT after surgery for brain tumours. The aim is to kill any cells left behind. The trial team are comparing 2 different PDT laser wave lengths. One shines deeper into brain tissue than the other. Doctors want to know which wave length of laser is better at stopping brain tumours coming back after surgery.
An experimental treatment that uses electric fields to disrupt and interfere with the division of cancer cells has been developed. It was used in the phase 3 EF-11 trial in the USA, Europe and Israel. The device is battery powered and gives low amplitude alternating electric fields through disposable electrodes stuck to the scalp. In the trial, 120 patients with glioblastoma that had come back used the electrical field device for about 20 hours each day. A similar number of patients had the standard chemotherapy for recurrent glioblastoma.
The trial seemed to show that the electrical field therapy may work as well as chemotherapy for glioblastoma that has come back after previous treatment. The researchers say that the electrical field therapy seems to be safe and the only side effects reported were skin irritation from the electrodes. However, some researchers were concerned about the design of the trial. We need more research into electric field treatment before we know how helpful it may be for brain tumours.
The main ingredients of the drug Sativex are tetrahydrocannabinol (THC) and cannabidiol (CBD). Both of these come from the cannabis (marijuana) plant. An early trial is looking at Sativex with temozolomide for glioblastoma multiforme that has come back after treatment. The researchers want to find out how well this combination of treatment works and what the side effects are.
The British Childhood Cancer Survivor Study is following children who’ve had successful cancer treatment. The researchers are looking at their health in the years following their cancer treatment to see how it has been affected. They are also monitoring their general quality of life, how they do in school, and whether or not they go on to have children of their own. It is important that we understand the long term effects of treatments so that we can improve them in years to come. If we can identify some of the risks, doctors may be able to take steps to prevent other health problems from developing.
Children who’ve been treated for other types of cancer in the past may have an increased risk of getting a brain or spinal cord tumour in the future. This type of study can help doctors to predict who is at risk. If they knew that, they may be able to take action to reduce the risk for these patients.
There is more about the potential effects of brain tumour treatment on children in this section of the website.
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