Bevacizumab (pronounced bev-ah-siz-oo-mab) is under much debate for use in the treatment of brain tumours. Although effective in treating other forms of cancer, the evidence for its effectiveness in brain tumours is not clear. For this reason, it is not licenced for use in the UK to treat brain tumours.
It is, however, being used in some clinical trials e.g. for high grade gliomas in both adults and children, particularly in combination with chemotherapy and/or radiotherapy.
Its brand name is Avastin®.
Bevacizumab is a type of 'monoclonal antibody'.
Antibodies are naturally occurring proteins within our bodies that our immune system makes when it detects harmful substances. The antibodies work to remove or kill the harmful substances.
Researchers have learned how to make antibodies that detect specific substances, known as 'markers', on the surface of some tumour cells. When many exact copies of that antibody are made, they are called Monoclonal Antibodies (MABs).
Bevacizumab works by attaching itself to markers on the tumour cells' surface and blocking signals that help the cells to grow or divide.
Some studies initially produced promising results in shrinking recurrent glioblastomas. These are glioblastomas (GBMs) that have returned after initial treatment.
This led to accelerated approval of the drug in the USA. However, in Europe it was felt that this shrinking could be due to bevacizumab's effect of reducing swelling in and around the tumour rather than shrinking the tumour itself. As a result, Europe (including the UK) have not authorised it for treatment of brain tumours.
"Currently, no data have shown whether or not Avastin improves disease-related symptoms or survival in people previously treated for GBM."
New research is looking at following treatment with bevacizumab with a drug called dasatinib (Sprycel®). This is only available within clinical trials.
Results from trials on newly diagnosed glioblastoma - some have shown no worsening of symptoms (known as 'progression-free survival'), but others have shown little or no effect.
There has been no effect on overall survival.
The evidence currently suggests it may not be suitable as first line use in newly diagnosed patients.
Research into whether bevacizumab is helpful in treating other brain tumours is ongoing within clinical trials. These include recurrent grade 2 and 3 gliomas, and grade 3 and 4 non-brainstem gliomas in children.
As it is not licensed in the UK, it is very unlikely that you will be able to have bevacizumab.
If your medical team believes it would benefit you, they may be able to help you to access to the drug via the following routes:
If your medical team does not think bevacizumab would benefit you, you are entitled to request a second opinion from another health professional. Your GP or your neuro-oncologist can help to arrange this.
Bevacizumab is taken 'intravenously' i.e. directly into your vein, usually over a series of sessions every two to three weeks.
It is sometimes taken in combination with chemotherapy or radiotherapy.
The most common side-effects of bevacizumab include:
The most common serious side-effects of bevacizumab include:
These side-effects can sometimes be life-threatening. Contact your health care team if you have any signs of side-effects, or any of the following:
Bevacizumab can also affect vaccinations, pregnancy, breast feeding and use of other medicines. Speak to your health team.
If you have further questions, need to clarify any of the information on this page, or want to find out more about research and clinical trials, please contact our team:
0808 800 0004 (free from landlines and mobiles)
01252 749 999
Phone lines open Mon-Fri, 09:00-17:00
You can also join our active online community on Facebook - find out more about our groups.