Common questions about targeted therapy

You may have many questions about having targeted therapy as part of your cancer treatment. Below are some answers to common questions people may ask. Your cancer care team can provide more detail about your individual situation.

Learn more about:

• Will targeted therapy work?
• How do I get targeted therapy?
• How much will it cost?
• How is targeted therapy given?
• What side effects will I have?
• How will I know if targeted therapy is working?

Will targeted therapy work?

The cancer must contain the particular target or the targeted therapy drug won’t work. The response to targeted therapy varies widely. In some cancers, four out of five people assessed as suitable for a particular targeted therapy drug will respond, while for other cancers, the rate of success is much lower. This is due to a range of factors, including how many of the cancer cells carry the target.

Cancer cells can eventually stop responding to a targeted therapy drug even if it works at first. If this happens, another targeted therapy drug or another treatment may be offered. Less commonly, a targeted therapy drug may cause serious side effects and the treatment plan will need to be adjusted.

How do I get targeted therapy?

Ask your cancer specialist if there is a suitable targeted therapy for you. This will depend on the type and stage of the cancer. Your specialist will also need to test the cancer to see if one of the currently available drugs is an option.

Many more targeted therapy drugs are being studied in clinical trials. Talk with your specialist about the latest developments and whether there are any trials that might be right for you.

For more on clinical trials, see Clinical trials and research.

How much will it cost?

The Pharmaceutical Benefits Scheme (PBS) covers most of the cost of many prescription medicines, including some targeted therapy drugs. Medicines not on the PBS are usually expensive, but you may be able to have them as part of a clinical trial or at a reduced cost through a compassionate access program.

How is it given?

Targeted therapy is usually prescribed by a medical oncologist or haematologist. It may be given on its own or combined with chemotherapy.

Some targeted therapy drugs are given in repeating cycles, with rest periods. Others are taken every day without any breaks. Most cancers have treatment protocols that set out which drugs to have, how much and how often.

You can find information about protocols for targeted therapy and other cancer drugs at eviq.org.au. Your specialist may need to adjust the protocols to your individual situation.

Targeted therapy may be given in different ways:

• as tablets or capsules that you can swallow
• as an intravenous (IV) infusion into a vein, either through a drip in your arm or into a port (a small device inserted under the skin of the chest or arm)
• as an injection under the skin.

When targeted therapy is given as an infusion, some people react to the infusion process (e.g. skin rashes, nausea, difficulty breathing). Reactions can occur during or several hours after the infusion. You will be monitored and may be given medicine to help prevent this. Reactions are more common with the first infusion, so it may be given more slowly than later treatments.

How long you have targeted therapy depends on the aim of the treatment, how the cancer responds and any side effects you have. In many cases, targeted therapy tablets or capsules need to be taken daily for many months or even years. Your treatment team can give you more details.

You will usually not need to take any special precautions to protect other people in your household while you are having targeted therapy.

What side effects will I have?

Read about common side effects and how they are managed.

How will I know if it’s working?

You will have regular check-ups with your doctor, blood tests and different types of scans to see whether the cancer has responded to treatment.

A good response from targeted therapy will make a cancer that can be seen on a scan shrink or even disappear completely.

In some cases, the cancer remains stable, which means it doesn’t grow in size on scans, but also does not shrink or disappear. People with stable disease can live for many years and have a good quality of life.