What happens when you start chemotherapy?
Answer: Jeni Jones, Support Manager, Pancreatic Cancer
UK
The first thing to remember before commencing chemotherapy
treatment is that you need to sign a consent from, which is your
agreement to undergo the treatment. At this point, you can
ask any unanswered questions and discuss any concerns with your
oncology team.
If you have been offered chemotherapy for a diagnosis of pancreatic
cancer, then it is likely that you will have been offered
Gemcitabine. This is the most commonly used drug for pancreatic
cancer in the UK. It can also be used to treat other cancer types
ie: breast, bladder or lung cancers, but this is usually in
combination with other drugs.
Chemotherapy is given in CYCLES. These cycles are at an equal
interval apart, which allows for the specific action of the drug to
take place. Most of the time, each cycle will only contain one dose
of drug treatment. However, in the case of pancreatic cancer, each
cycle contains 3 separate doses of the drug. The cycle is a 4
weekly regime - 3 weeks where you will have one dose of the drug
per week, and 1 week which is your "week off". This is known
as 'Day 1, Day 8 and Day 15' and you will often hear the staff
involved in your care talking about these specific days. Each
chemotherapy prescription is prescribed and ordered on an
individual basis. The dose is based on each patient's height,
weight and body surface area.
The gemcitabine is given as an infusion, over 30 minutes. You will
have a small plastic tube (cannula) inserted into one of your
veins, and will be attached to a drip. The drip will more than
likely be fed through a pump, which is programmed to deliver the
chemotherapy at the correct time, and correct rate. After this is
finished, the nurses will attach a small bag of fluid to "flush"
through the line, thus making sure the entire drug has left the
line, and making it safe to remove the cannula.
It is very important that if you feel any burning, pain or tingling
at the vein site during the infusion, that you alert the nursing
staff immediately. Very occasionally, gemcitabine can cause pain
along the vein as it is being infused. Although this is uncommon,
it is something which should be attended to straight away. It may
be that the cannula has become dislodged, and the drug is infusing
into the tissue, and not into the vein. The staff will stop the
infusion while they check the vein site and make sure it is still
in the correct place and working properly. If there is a
problem with pain during the infusion, then it may be that the
infusion time has to be extended in order to complete it
successfully. If this happens, then usually all subsequent
infusions will be given over a longer time.
Generally speaking, you will need to be seen by the oncologist at
the start of each cycle. During this appointment, you will have
blood tests taken to ensure that it is safe to continue on with the
next cycle. These will include a full blood count (FBC for short),
kidney function tests, liver function tests and usually, tumour
markers. The tumour marker used for pancreatic cancer is called CA
19.9. You may hear this being spoken about. On its own, this is not
an indicator for what is happening with the cancer, but helps build
a picture alongside other tests such as CT scans. The doctor will
also take into account the clinical picture of the patient in front
of them, for example, the person may be feeling a lot better having
had chemotherapy, even though sometimes the scans do not show a
change in the tumour. You will also be weighed, and your weight
will be monitored throughout your treatment.
During this appointment, the doctor will ask you about any
side-effects you experienced from the previous cycle of
chemotherapy. It is a good idea, if you are able, to keep a brief
diary of what these are. The specific questions the team might ask
are the lengths of time which the side effects lasted for e.g. if
you had had diarrhoea, when did it start and how long did it last.
This may be important for influencing a decision on whether to
reduce the dose of the drugs or not. Most side effects are graded
from 0-4; 0 being no side effect and 4 being severe side effects.
The oncologist will go through a specific list and ask you how you
tolerated the chemotherapy. At this stage, if necessary, any
medication changes or dose alterations can be done e.g. changing an
anti-sickness drug to a stronger type, or reducing the dose of the
chemotherapy. You may also have a physical examination of your
heart and lungs, especially if you are on a clinical trial. If you
have nothing to report, this may be omitted.
Once your blood results are back, the doctor or nurse will be able
to tell you if you blood count levels are adequate for you to go
ahead with the next cycle of chemotherapy. Some hospitals do not
have the facility for all the blood results to be done quickly, so
you may have to wait a day or two before having your treatment. You
will be given an appointment to see the doctor again prior to your
next cycle. If you do not have this before you leave the hospital,
you should ask at the appointment desk.