What are spinal cord tumours?
Spinal cord tumours are rare. They can start in the:
- spinal cord
- nerves that branch out from the spinal cord
- layers of tissue that protect the brain and spinal cord (the meninges).
There are several different types of tumour that can start in the spinal cord. The most common are:
- ependymomas
- astrocytomas
- meningiomas
- nerve-sheath tumours, such as schwannomas or neurofibromas
- haemangioblastomas.
This information is about primary spinal cord tumours. These are tumours that have started in the spinal cord itself.
If a spinal tumour has spread from somewhere else in the body to the spinal cord, or to the bones which surround the spinal cord (vertebrae), it is called a secondary or metastatic spinal tumour. These tumours are treated differently to primary spinal cord tumours.
When a tumour that has spread from somewhere else in the body causes pressure on the spinal cord, this is called metastatic spinal cord compression, or malignant spinal cord compression (MSCC).
We have more information about treatment for secondary cancer in the spine and malignant spinal cord compression.
Related pages
Symptoms of spinal cord tumour
Symptoms depend on the position of the tumour in the spinal cord. Spinal cord tumours often cause symptoms by pressing on the spinal cord or nerves. This can cause:
- weakness and numbness in the arms and legs
- clumsiness or difficulty walking
- back or neck pain
- aching in the spinal area, arms or legs
- tingling or pins and needles in the hands or feet
- loss of bladder and bowel control (incontinence)
- problems with sex, such as erectile dysfunction.
Related pages
Causes of spinal cord tumour
The causes of spinal cord tumours are unknown, but research is being done to find out more.
In a small number of cases, spinal cord tumours may be linked with inherited (genetic) conditions such as:
- neurofibromatosis syndrome
- von Hippel-Lindau syndrome.
People affected by these have a higher risk of some types of spinal cord tumour.
Diagnosis of spinal cord tumour
Your doctors need to find out as much as possible about the type, position and size of the tumour, so they can plan your treatment.
You will have:
- an MRI scan or a CT scan to find out the exact position and size of the tumour
- do a physical examination of parts of your nervous system, such as, tests on your reflexes and the power and feeling in your arms and legs
- blood tests to check your general health.
Related pages
Grading of a spinal cord tumour
Your doctor may talk about the grade of a tumour. The grade of a tumour describes how abnormal the cells look under a microscope. This can help your doctor understand how quickly a tumour might grow and whether it is likely to spread. Tumours that start in the spinal cord can be low-grade or high-grade.
Low grade spinal cord tumour
Most spinal cord tumours are low-grade. This means they grow slowly. They are sometimes called benign tumours. Low-grade spinal cord tumours do not usually spread to other parts of the brain or spine. But they may cause problems by continuing to grow and pressing on nearby nerves or the bones of the spine.
High-grade spinal cord tumour
High-grade spinal cord tumours grow more quickly. They are also called malignant tumours. They can grow into nearby tissues. They can also spread to lower down the spinal cord or the brain. Spinal cord tumours do not usually spread to other parts of the body.
We have more information about grading of brain and spinal cord tumours.
Treatment for spinal cord tumour
The main treatments used for spinal cord tumours are surgery, radiotherapy and steroids.
Your treatment depends on:
- your general health
- the size, position and type of the tumour
- your symptoms.
A team of specialists will plan your treatment. Your specialist doctor and nurse will explain the aims of your treatment and what it involves. They will talk to you about the benefits and risks of different treatment types. They will also explain the side effects.
You may be given a choice of treatment options. You will have time to talk about this with your hospital team before you make any treatment decisions.
You will need to give permission (consent) for the hospital staff to give you the treatment. Ask any questions about anything you do not understand or feel worried about. Tell your specialist doctor if you need more information or more time to decide on a treatment.
Related pages
Surgery
Surgery is the main treatment for many types of spinal tumours. If your surgeon cannot remove the tumour completely, they may be able to remove part of it. This is called debulking surgery. It can improve your symptoms by relieving the pressure on the spinal cord and nerves.
During surgery, the surgeon will take a sample of cells from the tumour (biopsy). This will be examined to find out what type of tumour you have. It can help your doctors plan further treatment, if needed.
After surgery, you may be looked after in a high dependency unit or on the ward for a few days. Your surgeon will give you more information about what to expect.
Sometimes it is not possible to remove the tumour. In this situation, the surgeon may only take a biopsy. Or it may be possible to diagnose the type of tumour you have from how it looks on the MRI scan.
Radiotherapy
Radiotherapy uses high-energy rays to destroy tumour cells and control the tumour. You may have radiotherapy:
- as the main treatment when surgery is not possible
- if the doctor thinks the tumour is likely to respond very well to radiotherapy (radiosensitive)
- after surgery if the tumour cannot be completely removed
- to reduce the risk of the tumour coming back
- if a tumour comes back.
Steroids
Doctors may sometimes prescribe steroid drugs to help reduce the swelling around spinal cord tumours. They can reduce the symptoms caused by increased pressure and make you feel better. They may be given before or after surgery, and during or after radiotherapy. The most commonly used steroid is called dexamethasone, but other types can also be used.
It is important to take them exactly as your doctor has explained. Do not stop taking steroids suddenly without talking to your doctor or specialist nurse first. Tell them if you are worried about any side effects of steroids. These will go away gradually as your doctor reduces your steroid dose.
Active monitoring
Active monitoring means regularly checking the tumour to find out if it is growing.
If the scans of your spine suggest that the tumour is slow growing (low-grade), and it is not causing you problems, your doctor may suggest active monitoring instead of starting treatment straight away. This is also called active surveillance or watch and wait.
Active monitoring means regularly checking the tumour with MRI scans to find out if it is growing or changing. You may see your specialist doctor regularly to discuss the results of your scans. This can help your doctor know if and when to recommend treatment. They may suggest a biopsy (an operation to remove a small piece of the tumour) to confirm the diagnosis.
Low-grade spinal tumours may grow only very slowly. Treatment can cause side effects and some of these may be permanent. Active surveillance may be suggested if the side effects of treatment might outweigh the benefits.
Talk to your specialist doctor or nurse if you are worried about any symptoms.
Chemotherapy
Chemotherapy uses anti-cancer drugs to destroy tumour cells. It is rarely used for spinal tumours. Side effects of chemotherapy depend on the drugs you have. Your doctor will talk to you about chemotherapy treatment, if it is suitable for you.
Clinical trials
Clinical trials are a type of medical research involving people. They are important because they show which treatments are most effective and safe. This helps healthcare teams plan the best treatment for the people they care for.
Trials may test how effective a new treatment is compared to the current treatment used. Or they may get information about the safety and side effects of treatments.
They will give you information about the clinical trial so that you understand what it means to take part. If you decide not to take part in a trial, your specialist doctor and nurse will respect your decision. You do not have to give a reason for not taking part. Your decision will not change your care. Your doctor will give you the standard treatment for the type of tumour you have.
Clinical trials also research other areas. These include diagnosis and managing side effects or symptoms. As these tumours are rare, there may not always be a relevant clinical trial happening. If there is, your doctor or nurse may ask you to think about taking part.
We have more information about clinical trials.
Side effects of treatment for a spinal cord tumour
Your specialist doctor or nurse will explain your treatment and possible side effects. Most side effects are short-term and will improve gradually when the treatment is over. Some treatments can cause side effects that can continue and may not get better. These are called long-term effects. You may also get side effects that start months or years later. These are called late effects. We have more information about coping:
After treatment for spinal cord tumour
After your treatment has finished, you will have regular follow up appointments, tests and scans. How often you are seen and for how long may vary depending on the size and grade of the tumour, and the treatment you have had.
You may still have some side effects from treatment. These may include tiredness, or problems with mobility.
Some side effects can start months or years after treatment has finished. You can use your follow-up appointments to talk about these side effects, or about any other worries or problems you have.
Your doctor or nurse may refer you to a neurological rehabilitation (neuro-rehab) service. This service may be able to refer you to a physiotherapist or occupational therapist and offer emotional support.
Many people find they get very anxious before appointments. This is natural. It may help to get support from family, friends or a specialist nurse.
How diagnosis affects your right to drive
How a spinal cord tumour might affect your right to drive will depend on what symptoms you have and your individual situation. Your doctor, surgeon or specialist nurse will tell you if this applies to you.
If you have a driving licence, you must tell the vehicle licensing agency (DLVA or DVA) that you have been diagnosed with a spinal tumour.
You can find out more information on the following websites:
- If you live in England, Scotland or Wales, contact the Drivers and Vehicle Licensing Agency (DVLA).
- If you live in Northern Ireland, contact the Driver and Vehicle Agency (DVA).
You can be fined if you do not tell the DVLA or DVA about a medical condition that affects your driving. If you continue to drive when you have been advised not to, you:
- will not be covered by your insurance
- could be prosecuted if you have an accident.
Getting support
Being diagnosed with a spinal tumour may cause a range of different emotions. There is no right or wrong way to feel. It may help to get support from family, friends or a support organisation.
Macmillan is also here to support you. If you would like to talk, you can:
- Call the Macmillan Support Line for free on 0808 808 00 00.
- Chat to our specialists online.
- Visit our brain cancer forum to talk with people who have been affected by brain tumours, share your experience, and ask an expert your questions.
You may also want to get support from a brain tumour charity, such as:
About our information
This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.
-
References
Below is a sample of the sources used in our information about spinal cord tumours. If you would like more information about the sources we use, please contact us at informationproductionteam@macmillan.org.uk
Kumar N, Tan WLB, Wei W, Vellayappan BA. An overview of the tumors affecting the spine-inside to out. Neurooncol Pract. 2020 Nov 18, 7. Available from: www.ncbi.nlm.nih.gov/pmc/articles/PMC7705529/ [accessed August 2024].
NICE Guideline NG99. Brain tumours (primary) and brain metastases in over 16s. 2018 (updated 2021). Available from: www.nice.org.uk/guidance/ng99 [accessed June 2024].
Date reviewed
Our cancer information meets the PIF TICK quality mark.
This means it is easy to use, up-to-date and based on the latest evidence. Learn more about how we produce our information.
The language we use
We want everyone affected by cancer to feel our information is written for them.
We want our information to be as clear as possible. To do this, we try to:
- use plain English
- explain medical words
- use short sentences
- use illustrations to explain text
- structure the information clearly
- make sure important points are clear.
We use gender-inclusive language and talk to our readers as ‘you’ so that everyone feels included. Where clinically necessary we use the terms ‘men’ and ‘women’ or ‘male’ and ‘female’. For example, we do so when talking about parts of the body or mentioning statistics or research about who is affected.
You can read more about how we produce our information here.
How we can help