Chemotherapy treatment uses anti-cancer medicines (drugs) to treat cancer by stopping cells from growing, or by destroying cells.
Your child may have several types of chemotherapy because each type of chemotherapy medicine stops cell growth or destroys cells in a different way.
When chemotherapy destroys cancer cells, it can also damage healthy cells. This damage can cause side effects. Often, the side effects get better or go away once the chemotherapy treatment ends. Different drugs have different side effects. Each child can react differently to the same chemotherapy drug.
Your child may receive chemotherapy treatment:
Your child will have chemotherapy in one or more of these ways. How your child receives chemotherapy will depend on the type of cancer they have and the chemotherapy medicines that work best for that type of cancer.
Soon after your child's cancer diagnosis, your child's healthcare team will give you a treatment plan, often called a treatment protocol.
This will have details of the treatment and the names of the medicines the doctors will use. It will also explain how and when the medical team will give the medicines.
Your child's healthcare team will also give you information sheets about the medicines that your child will have and the possible side effects. The information sheets will also tell you if you need to protect you and your family from contact with these medicines. This is because some medicines stay in wee (urine), poo (faeces) and blood up to 48 hours after chemotherapy treatment ends.
In most cases, chemotherapy happens in cycles. A cycle is a period of chemotherapy treatment followed by a rest period. The rest period allows time for your child's body to build healthy new cells before the next treatment. For example, your child may have chemotherapy for 1 week and then have 2 weeks of rest. These 3 weeks make up 1 cycle.
Your child's healthcare team will give you information about your child's chemotherapy schedule. They will also list all the chemotherapy medicines that your child will have.
See patient information sheets for a range of chemotherapy drugs [1]
After your child has chemotherapy, their body sometimes gets rid of small amounts of the drugs in body fluids including blood, wee, poo or vomit. The amount will vary depending on the kind of drug they have.
Read more about childhood cancer treatments [2]
Many chemotherapy medicines cannot tell the difference between normal cells and cancer cells. These medicines affect all cells that divide rapidly. The damage to normal cells may lead to side effects. Different chemotherapy medicines cause different side effects.
Since children respond to chemotherapy differently, some children will experience more side effects than others. Your child's healthcare team will manage the side effects, as they develop, to keep your child as comfortable as possible. Because normal cells can repair themselves, the side effects are nearly always temporary.
Chemotherapy medicines most often affect the normal cells in the:
Tell your child's doctor or nurse if you think the medicine is causing other side effects.
It can help to keep all the following in one place:
Oral chemotherapy is just like taking any other medicine by mouth. It does not hurt but if your child does not like medicines, the nurse or hospital play specialist will give you some hints to help make it easier for them.
You may be able to give chemotherapy to your child by mouth at home. If this is an option, the nursing staff or pharmacist will teach you about this.
A doctor or nurse may inject the medicine into your child's muscle (intramuscular injection). This may sting.
A doctor or nurse may give an injection under your child's skin (subcutaneous injection). If this happens, your child's nurse will first put a numbing (anaesthetic) cream on your child's skin. This will make the area feel numb. Either a nurse will put the cream on your child's skin, or show you how to do it yourself.
If your child needs an injection into the fluid around the spinal cord (intrathecal injection), this will happen under general anaesthetic so your child will be asleep and will not feel anything.
If your child has an external catheter, a nurse will put the medicine into the tubing so there is no skin prick.
If your child has an internal catheter, you or a nurse can put an anaesthetic cream on your child's skin over the port. This will numb your child's skin before the nurse puts the needle in.
Not always.
Your child can have chemotherapy tablets or liquid (suspension) at home.
Your child may receive some kinds of chemotherapy at an outpatient clinic or day-stay unit of the hospital. Your child may receive the medication:
Some chemotherapy is complex. If your child needs this kind of chemotherapy, they will need to go to hospital. Your healthcare team will discuss this with you and it will be in the treatment plan (treatment protocol).
All the pages in the childhood cancer section of this website [3] have been written by health professionals who work in the field of paediatric oncology. They have been reviewed by the members of the National Child Cancer Network (NZ). Medical information is authorised by the clinical leader of the National Child Cancer Network.
This page last reviewed 13 May 2021.
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Links
[1] https://kidshealth.org.nz/chemotherapy-drugs-information-patients-families
[2] https://kidshealth.org.nz/tags/childhood-cancer-treatments
[3] https://kidshealth.org.nz/tags/childhood-cancer
[4] https://kidshealth.org.nz/contact?from=http%3A%2F%2Fkidshealth.org.nz%2Fprint%2F455%3Flanguage%3Dmi