Page last updated: November 2025
The information on this webpage was adapted from Understanding Brain Tumours - A guide for people with cancer, their families and friends (2024 edition). This webpage was last updated in November 2025.
Expert content reviewers:
This information was developed based on Australian and international clinical practice guidelines, and with the help of a range of health professionals and people affected by brain tumours:
- Prof Lindy Jeffree, Director of Neurosurgery, Alfred Health, VIC
- Caitriona Nienaber, 13 11 20 Consultant, Cancer Council WA
- Prof Tamara Ownsworth, Clinical Neuropsychologist and Research Director, The Hopkins Centre, Griffith University, QLD
- A/Prof Hao-Wen Sim, Medical Oncologist, The Kinghorn Cancer Centre and Chris O’Brien Lifehouse, NSW
- Megan Trevethan, Clinical Specialist Occupational Therapy – Cancer and Lymphoedema Services, Princess Alexandra Hospital, QLD
- Chris Twyford, Cancer Specialist Nurse, Canberra Health Services, Cancer and Ambulatory Support, ACT
- Dr Adam Wells, Clinical Academic Consultant Neurosurgeon, The University of Adelaide, Royal Adelaide Hospital, SA
Treatments offered for a brain or spinal cord tumour will depend on:
- the type, size, grade, location and genetic make-up of the tumour
- your age, medical history and general state of health
- the symptoms you have
- the aim of treatment – whether to remove as much of the tumour as possible; to slow the tumour’s growth; or to relieve symptoms by shrinking the tumour and reducing swelling.
The tumour type may not be known for certain until after a biopsy or surgery. Treatment is planned by what the surgeon thinks the tumour may be from scans.
For a benign tumour, surgery may be the only treatment. For a malignant tumour, treatment may include surgery, radiation therapy, and drug therapies such as chemotherapy or targeted therapy.
Medicines, such as steroids or anticonvulsants, may reduce symptoms or manage seizures. You may have a new or modified treatment, such as immunotherapy, on a clinical trial.
Your guide to best cancer care
A lot can happen in a hurry when you’re diagnosed with cancer. The guide to best cancer care for brain tumours (high grade glioma) can help you make sense of what should happen.
It will help you with what questions to ask your health professionals to make sure you receive the best care at every step.
Read the guide
Surgery
Surgery in the brain or spinal cord is called neurosurgery. You may have surgery to:
- remove the whole tumour (total resection)
- remove part of the tumour (partial resection or debulking)
- help diagnose a brain tumour (biopsy).
All of the tumour will be removed if it can be done safely, but this will depend on the type and location of the tumour.
Removing part of the tumour may be considered when the tumour covers a wider area or is near major blood vessels or other important parts of the brain or spinal cord. This may help reduce the pressure on your brain, which will improve some of the symptoms.
Having surgery to the brain can sound frightening and it is natural to feel anxious beforehand. Talk to your treatment team about your concerns or call Cancer Council 13 11 20 for support.
When surgery is not possible
Sometimes a tumour is considered unsafe to remove because it is too close to certain parts of the brain, and surgery would cause blindness, loss of speech, paralysis or other serious complications. These may be called inoperable or unresectable tumours.
A needle biopsy is still often possible and can help to guide treatment options. Your doctor will talk to you about what treatments you can have and ways to manage symptoms.
What to expect before surgery
The different scans used to diagnose a brain tumour (such as MRI or CT scans) are often done again to plan surgery. Some people may have a functional MRI (fMRI) to help the surgeon avoid damaging the most important areas of the brain.
You will be asked to complete brain exercises during the MRI scan to show the exact areas of the brain that are used as you speak or move. These parts of the brain can also be found during surgery with brain mapping.
Tell your doctor about any blood-thinning or other medicines, and any supplements that you take. Some medicines interfere with the anaesthetic used during the operation, so you may need to stop taking them for a while.
If you smoke or vape, it is important to stop before surgery, as smoking or vaping can increase the risk of complications.
Types of surgery
Different types of surgery may be used for brain and spinal cord tumours.
Removing a brain tumour (craniotomy)
This is the most common type of brain tumour surgery. A craniotomy removes all or part of the tumour (total or partial resection) and may be done under a general anaesthetic.
The surgeon cuts an area of bone (called the bone flap) from your skull to access the brain and remove the tumour. The bone is then put back and a small plate is screwed on to hold the piece of skill in place.
If you have a high-grade glioma, you drink a solution before surgery to make the tumour glow under a special blue light. This helps the surgeon remove as much of the tumour as possible, while avoiding normal brain tissue.
Brain mapping
An electrode is placed on the outside layer of the brain to stimulate and pinpoint important areas of the brain. Brain mapping may be done during surgery, or as part of an awake craniotomy.
Awake craniotomy
This operation may be recommended if the tumour is near parts of the brain that control speech or movement.
You are usually put to sleep (general anaesthetic) and are later woken up but relaxed (conscious) for part of the operation. The surgeon asks you to speak or move parts of your body to identify and avoid damaging those parts of the brain.
You may be worried that an awake craniotomy will be painful, but the brain itself does not feel pain and local anaesthetic is used to numb surrounding tissues.
Removing a pituitary tumour (endoscopic transsphenoidal surgery)
The most common surgery for pituitary gland tumours (and other tumours located near the base of the brain) is called endoscopic transsphenoidal surgery.
To remove the tumour, the surgeon inserts a long, thin tube with a light and camera (called an endoscope) through the nose and into the skull at the base of the brain. An ear, nose and throat (ENT) surgeon may also assist with this type of surgery.
You will be given a general anaesthetic for this operation.
Removing a spinal cord tumour (laminectomy)
The most common surgery for spinal cord tumours is a laminectomy. The surgeon makes an opening through the skin, muscle and a vertebra in the spinal column to remove the tumour. You usually have a general anaesthetic for this type of surgery.
Some spinal cord tumours may also need surgery to the spinal cord itself. Your surgeon will talk to you about this particular surgery, as it may have a risk of nerve or spinal cord injury.
What to expect after surgery
You will be closely monitored for the first 12–24 hours after the operation. For the first day or two, you will be in the intensive care or high dependency unit.
You may stay in hospital for only 2 or up to 10 days. How long you stay in hospital will depend on whether you have any problems or side effects after the surgery
- Checks and observations – nurses will regularly check your breathing, blood pressure, pulse, temperature, pupil size, and arm and leg strength and function. You will also be asked questions to assess your level of consciousness. These are called neurological observations, and help to check how your brain and body are recovering from surgery.
- Spinal cord checks – if you have had an operation on your spinal cord, the nurses will regularly check the movement and sensation in your arms and legs. You may need to lie flat in bed for 2–5 days to allow the wound to heal. A physiotherapist will help you learn how to roll over and how to get out of bed safely, to avoid damaging the wound.
- Pressure stockings – you will need to wear pressure stockings on your legs to prevent blood clots from forming while you are recovering from surgery. Tell your doctor or nurse if you have pain or swelling in your legs or suddenly have difficulty breathing.
- Rehabilitation – the surgery may cause a range of short-term or longer-term side effects. Before you can return home, you may need further treatment known as rehabilitation to help you regain your mobility and get back to your daily activities.
- Bandages and bruising – the wound is covered with a dressing, which varies from a small adhesive pad to bandaging covering your head. Some or all of your head may be shaved. After some surgery, your face and eyes may be swollen or bruised. It’s not usually painful and should ease in about a week. You may have dissolvable sutures (stitches) that don’t need to be removed, they simply fall out. Or you may have sutures or staples that need to be taken out once the wound has healed. You will have a scar, and your hair won’t grow in the scar – but it’s usually behind the hairline and once the rest of your hair grows back it isn’t easily seen
- Headaches and nausea – you may have a headache or nausea after the operation. Both can be treated with medicines.
- Having a shunt – rarely, there may be a build-up of cerebrospinal fluid in the brain, called hydrocephalus. It may be caused by the tumour or it can happen after surgery. To drain the extra fluid, you may have a temporary or permanent shunt (a long thin tube placed into your brain). For a temporary shunt (called an external ventricular drain), the tube drains fluid into a bag on the outside of the body. For a permanent shunt, the tube is inserted completely inside your body. It drains into your abdomen and the fluid is absorbed into your bloodstream.
Side effects of surgery
- Infection – although the risk is small, you may develop an infection at the wound site. This can usually be treated with antibiotics. A small number of people may need surgery to have the wound cleaned out and possibly the bone flap removed. Another surgery will usually be done later on to replace the missing area, for safety and to look natural.
- Bleeding – this is a rare but serious side effect. You will have a CT or MRI scan the day after surgery to check for any bleeding or swelling.
- Swelling – surgery can cause swelling in the brain, which increases the pressure inside the skull (intracranial pressure). Your medical team will monitor the swelling and try to reduce it with medicines.
- Other side effects – you may continue to feel confused and dizzy, have speech problems, weakness in parts of the body and seizures. You and your family or carers may be surprised that you may feel worse than before the surgery and worry that you are not recovering well. These side effects are normal and often improve with time.
Rehabilitation after surgery
Some people recover and can gradually return to their usual activities. For others, there are longer-term changes to speech, movement, behaviour and thinking.
A range of therapies can help recovery or show you ways to manage any longer-term changes. These therapies are known as rehabilitation. At first, you may have some rehabilitation therapies in the hospital or a rehabilitation facility.
Once you return home, you can continue rehabilitation therapies as an outpatient. You may also be given equipment to use at home. You will have other changes, such as not being able to drive for a while.
Computer-assisted surgery
It is now usual for a craniotomy to be done using a computer system to guide the surgeon (stereotactic surgery). The computer uses the results of planning scans to create 3D images of the brain and tumour.
During the operation, this allows the surgeon to see the scan images at particular places in the head and position the surgical instruments more precisely.
Stereotactic surgery is safer, more accurate and requires a smaller cut in the skull than non-computerassisted surgery.
Radiation therapy
Radiation therapy uses a controlled dose of radiation to kill or damage tumour cells in the area being treated. The radiation is usually in the form of x-ray beams.
For gliomas, radiation therapy is usually given after surgery, and sometimes with chemotherapy (chemoradiation).
Before you start radiation therapy, a radiation therapist will take measurements of your body and do a CT or MRI scan to work out the precise area to be treated.
Treatment is carefully planned to do as little harm as possible to the healthy brain tissue near the tumour. Radiation therapy itself is painless, though you may experience some side effects which your treatment team will discuss with you.
If you are having radiation therapy for a brain tumour, you will wear a special plastic mask over your face. If you are having radiation therapy for a spinal cord tumour, some small marks may be tattooed on your skin to show the treatment area.
How often you have radiation therapy (the treatment course) will depend on the size and type of tumour. Usually it is given once a day, from Monday to Friday, for several weeks (often 3–6 weeks, but this varies person to person).
During treatment, you will lie on a table under a machine called a linear accelerator (LINAC). Most machines use daily imaging scans to check you are in the correct position for treatment. Each treatment will last for about 10–15 minutes.
Types of radiation therapy
Stereotactic radiosurgery (SRS)
Stereotactic radiosurgery (SRS) is a specialised type of radiation therapy, not a type of surgery, and no cuts are made in the skull. A specialised radiation machine is used to give very precisely targeted radiation to the tumour.
Machine types include LINAC, Gamma Knife and CyberKnife. They deliver a high dose of radiation to the tumour while the surrounding healthy brain tissue receives very little.
SRS is not suitable for all types of brain tumours. It may be offered when neurosurgery is not possible, or as an alternative. It is mostly used for cancers that have spread to the brain from another part of the body.
Some meningiomas, pituitary tumours, schwannomas, and occasionally gliomas that have come back, may be treated this way. Often, only 2–3 doses of SRS are needed (though you may have 1–5 doses as treatment is personalised).
A treatment session may last 15–45 minutes, depending on the type of radiosurgery given. You will need to wear a special mask (see opposite) or frame during the treatment. You will usually be able to go home after the session ends.
Stereotactic radiation therapy (SRT)
A stereotactic radiosurgery machine may also be used to deliver a longer course of radiation, particularly for benign brain tumours. This is called stereotactic radiation therapy or SRT. The treatment is given as multiple small daily doses.
Proton therapy
This uses protons rather than x-ray beams. Protons are tiny parts of atoms with a positive charge. Proton therapy is used for some types of brain and spinal cord tumours, and tumours near sensitive areas.
A proton therapy machine has been installed in South Australia. It is hoped it will start treating patients soon. Currently, there is funding in special cases to allow Australians to travel overseas for proton therapy.
Side effects of radiation therapy
Radiation therapy side effects generally occur in the treatment area and are usually temporary, but some may last for a few months or years, or be permanent.
The side effects vary depending on whether the tumour is in the brain or spinal cord, and may include:
- nausea – can occurs several hours after treatment
- headaches – can occur throughout the course of treatment
- tiredness or fatigue – worse at the end of treatment, can continue to build after treatment, but usually improves over a month or so
- dry, itchy, red, sore or flaky skin – may occur in the treatment area, usually mild and happens at the end of treatment and lasts 1-2 weeks before going away
- hair loss – may occur in a patch in the area of the head receiving treatment; usually temporary but in some cases permanent; if hair grows back, the texture or colour may be different
- dulled hearing – may occur if fluid builds up in the middle ear and is usually temporary but may be permanent.
Radiation therapy side effects for spinal cord tumours may include sore or dry throat and swallowing problems (if the neck area is treated) or diarrhoea (if the lower spine is treated). Both are temporary.
Talk to your radiation oncology team about how to manage any side effects.
A small number of adults who have had radiation therapy to the brain have side effects that appear months or years after treatment. These are called late effects, and can include symptoms such as poor memory, confusion and headaches.
High-dose radiation to the pituitary gland can cause it to produce too little of some hormones. This can affect body temperature, growth, sleep, weight and appetite. The hormone levels in your pituitary gland will be monitored during and after treatment.
Wearing an immobilisation mask
You’ll need to wear an immobilisation mask during radiation therapy to the brain. It helps keep your head still so that the radiation is targeted at the same area during each session.
The mask is made to fit you and fixed to the table when the radiation treatment is given. The mask is made of a tight-fitting plastic mesh that you can see and breathe through.
It may feel strange and confined but you usually only wear it for about 10 or 20 minutes at a time. For some people, especially those with claustrophobia, the thought of wearing the mask can feel overwhelming.
The team may suggest that you try relaxation or breathing exercises or a psychologist can give you strategies to try. You may also be offered medicine to help you relax.
Tell the radiation therapist if wearing the mask makes you feel anxious. With support, many people get used to wearing it.
Chemotherapy
Chemotherapy uses drugs to kill or slow the growth of cancer cells. The aim is to destroy cancer cells while causing the least possible damage to healthy cells.
You may have chemotherapy after surgery or radiation therapy, or at the same time as radiation therapy (chemoradiation).
For a brain tumour, you usually have chemotherapy as capsules or tablets that you swallow, but you may also have it as a liquid through a drip inserted into your vein (intravenously).
A structure known as the blood–brain barrier helps protect the brain from substances in the blood, such as germs or chemicals. Only certain types of chemotherapy drugs can get through this barrier.
Temozolomide is the most commonly prescribed chemotherapy drug to treat grade 4 glioma brain tumours. It is given as a capsule you take at home.
You will be instructed to take it for a set number of days, which is then followed by a rest period. This is called a cycle. You are likely to have up to six cycles of temozolomide, though it may continue for longer.
Your doctor may suggest a different dosage or another chemotherapy drug that is more suitable for your situation. Other drugs include lomustine and PCV (procarbazine, lomustine and vincristine).
Side effects of chemotherapy
There are many possible side effects of chemotherapy, depending on the type of drugs you are given. Talk to your doctor about ways to reduce or manage any side effects you have.
Side effects are mostly mild with temozolomide and may include:
- nausea or vomiting
- tiredness, fatigue and lack of energy
- increased risk of infection
- mouth sores and ulcers
- diarrhoea or constipation
- loss of appetite
- skin rash
- liver damage
- breathlessness due to low levels of red blood cells (anaemia)
- low levels of platelets (thrombocytopenia), increasing the risk of abnormal bleeding
- reduction in the production of blood cells in the bone marrow; you will usually have regular blood tests to monitor your blood levels
- damage to ovaries or testicles, which can make you unable to have children naturally (infertile).
In some cases your hair may become thinner or patchy, but it is rare to lose all your hair with chemotherapy for brain and spinal cord tumours.
Targeted therapy
Targeted therapy is a drug therapy that targets specific features of cancer cells to stop the cancer growing or spreading.
These drugs circulate through the body, but work in a more focused way than chemotherapy and often have fewer side effects.
A range of new targeted therapy drugs are being developed to match the molecular profile of each person’s cancer cells.
For brain tumours, researchers are studying how to target genes such as BRAF, NTRK and IDH.
These advances will help make personalised treatments possible.
Learn more
"I had no real problems and the surgeon said they got it all, but I’d need radiation therapy and chemotherapy, just to mop up any stray cells. That floored me – I hadn’t needed them the first time." Ali
Treatments to control symptoms
Anticonvulsants
You may be given anticonvulsants to help control seizures which can also affect your mood and energy. An experienced counsellor, psychologist or psychiatrist can help you manage any mood swings or behavioural changes.
If you or your family are worried about side effects, talk to a doctor, nurse or call Cancer Council 13 11 20.
Steroids
Steroids (also known as corticosteroids) are made naturally in the body, but they can also be made and used as drugs. Brain tumours and their treatments can both lead to swelling in the brain. Steroids may help to reduce this swelling.
They can be given before, during and after surgery and radiation therapy. The most commonly used steroid for people with brain tumours is dexamethasone. It is usually given as a tablet but may be given in a vein (intravenously) if needed.
Side effects of steroids
The side effects you may experience with steroids depend on the dose and length of treatment:
- Short-term use – You may experience increased appetite and weight gain; trouble sleeping; restlessness; mood swings; anxiety; and, in rare cases, more serious changes to thinking and behaviour. In people who have diabetes, steroids can quickly lead to high or unstable blood sugar levels. These short-term side effects can be managed. Eating before taking steroids can reduce the chance of them irritating your stomach.
- Longer-term use – If steroids are taken for several months, they can cause puffy skin (fluid retention or oedema) in the feet, hands or face; high blood pressure; weight gain; unstable blood sugar levels; diabetes; muscle weakness; and loss of bone density (osteoporosis). You are more likely to get infections. Your doctor may change your dose to manage your side effects. Most side effects go away after treatment ends.
Immunotherapy
Immunotherapy is not currently a standard treatment option for primary brain tumours. This is in part because of the way the brain’s immune system works.
New immunotherapy drugs are being tested in clinical trials. These include:
- treatments to help the immune system better recognise cancer cells (e.g. nivolumab, pembrolizumab)
- vaccines against cancer cells (e.g. PEP-CMV, DCVax)
- viruses to infect cancer cells (e.g. PVSRIPO, G47Δ), and
- treatments that change the patient’s own immune cells (e.g. CAR-T cell therapy).
Immunotherapy may be used to treat certain types of cancer that have spread to the brain (metastasised).
Learn more
Palliative treatment
Palliative treatment helps to improve quality of life by managing the symptoms when a brain tumour is no longer curable. As well as slowing the spread of cancer, palliative treatment can relieve pain and help with other symptoms.
Treatment may include surgery, radiation therapy, chemotherapy or other medicines.
Palliative treatment is one aspect of palliative care, in which a team of health professionals aims to meet your physical, emotional, cultural, spiritual and social needs.
You can have palliative care services in the home as well as in a hospital or in residential care.
Brain tumour clinical trials
Cancer clinical trials are research studies that test whether a new approach to prevention, screening, diagnosis, or treatment works better than current methods and is safe.
There are clinical trials for brain tumours open to recruitment in Victoria. This list shows the most recently updated brain tumour studies on the Victorian Cancer Trials Link (VCTL).
Visit the VCTL to find more brain tumour clinical trials.