Herceptin® is a monoclonal antibody that blocks the effects
of the growth factor protein HER2 which transmits growth signals to breast
cancer cells. Some breast cancers have too much of this protein (HER2
positive cancers), which can cause the cancer to grow and spread more
quickly. Herceptin® can help stop this growth.
Herceptin®, also known as Trastuzumab, is only used to treat HER2 positive breast cancer. It is a white to pale yellow powder which is dissolved into a clear, colourless liquid and is administered intravenously either once a week or once every three weeks. It can be used either as a stand alone treatment or in conjunction with other chemotherapy.
For
several years, Herceptin has been an established part of treatment for
patients with advanced HER2 positive cancer that has spread throughout
the body. Adding Herceptin to chemotherapy increases the length of time
until the cancer progresses again and increases the duration of life.
Recent studies have shown that Herceptin is also beneficial in patients
with early stage HER2 positive cancer, where the cancer is limited to
the breast and underarm lymph nodes. Treatment of patients with early
breast cancer aims not only to extend life, as in advanced cancer, but
to cure the disease. International trials involving over 12,000 women
with early-stage HER2-positive breast cancer show that Herceptin given
with or after post-operative chemotherapy reduced the risk of the cancer
recurring by up to half, compared with chemotherapy alone. After 2-3 years,
around one third more patients who had received 1 year of Herceptin treatment
were alive and were free of disease among those than those who had not.
Human Epidermal growth factor Receptor 2 (HER2) is a member of a family of growth
factor receptors that are important for controlling cell growth. HER2 is present
in small amounts in normal breast cells and breast cancer. However, if a breast
cancer has either too many HER2 genes, (HER2 gene amplification) or produces large
amounts of HER2 protein (HER2 protein over expression) then it is called HER2
positive. About 25% of all breast cancers are HER2 positive and
these cancers tend to occur in younger patients, grow quickly, spread rapidly, and
have a higher rate of recurrence. Following surgery and standard chemotherapy, on average
across all types of breast cancer, 80% of women will be alive 10 years after
diagnosis. In comparison, only 50% of women with HER2-positive breast cancer
will be alive 10 years after diagnosis. The chance of survival for an individual
patient depends on the stage of the disease at diagnosis and the treatments
provided.
Yes. Knowing whether you do have HER2 positive breast cancer will impact on the
treatment options available to you. It is important that your doctor discusses
these options with you to ensure that you make the best informed decision
regarding your breast cancer treatment. A HER2 test should now be performed
routinely on all newly diagnosed breast cancer or a new breast cancer recurrence.
Don’t be afraid to ask for your HER2 result and request the test if
it has not been done.
Breast
cancer tissue removed from the body during a biopsy or surgery is sliced
and stained using the immunohistochemistry (IHC) test which measures the
HER2 protein levels using a scale from 0 through 1+, 2+ to 3+. If a breast
cancer is scored as 0 or 1+, it is considered negative and people in that
category do not benefit from Herceptin®. Women whose
breast cancer is scored as 3+ are the most likely to benefit from Herceptin®.
Women whose cancer is scored as 2+ may or may not benefit from Herceptin®.
The best way to find out is to further test the tumour sample with the
FISH test. So if your cancer is 2+, your doctor will ask for the FISH
test to be done.
The Fluorescence In Situ Hybridization (FISH) test illuminates the HER2 genes
in the tumour sample to see how many there are. If a FISH test detects more than
2 copies of the HER2 gene, this means that the cell is abnormal and the breast cancer
is called “FISH positive” which also means the cancer is now
called “HER2 positive”. These women are also more likely to
benefit from Herceptin®. If “FISH negative”,
then the women will not benefit from Herceptin®.
In three different ways:
First, it binds to the HER2 proteins on the surface of the
tumour cell and blocks signals for cell growth. This
may result in cancer cell death.
Second, when Herceptin® binds to the HER2 proteins
on the surface of the tumour cell, immune system cells
within the body recognise it as a foreign object and
attack, helping to more effectively kill the cancer cells.
Third, Herceptin® and chemotherapies can form a very
effective team. Herceptin® can enhance the effectiveness
of chemotherapy which attacks and damages the DNA in the nuclei of tumour
cells and causes cancer cell death.
Compared with chemotherapy drugs, the side effects of Herceptin®
are relatively mild. They may include fever and chills, weakness, nausea,
vomiting, cough, diarrhoea, and headache. These side effects are usually
associated with the first dose and not seen again. Some women being treated
with Herceptin®, however, have experienced heart
damage leading to a problem called congestive heart failure. For most
women, this effect on the heart has been temporary and has improved when
the drug is stopped. The risk of heart problems is about 3 times higher
when Herceptin® is given with anthracyclines,
a class of chemotherapy drugs that includes doxorubicin (Adriamycin) and
epirubicin (Ellence) and may not be reversible. Major symptoms are shortness
of breath and severe fatigue. Women experiencing these symptoms should
call their doctor right away.
Recent study results have indicated that administration of Herceptin® following standard chemotherapy significantly reduces the risk of recurrence for women with early-stage HER2 positive breast cancer by 36-46% with a 34% overall survival benefit after an average of 23 months follow-up. Increased spending on cancer drugs may actually save money in other areas of health by treating patients more effectively and earlier, thereforepreventing recurrence and advancement of cancer. This not only eliminates unnecessary worry and suffering by patients but also makes economic sense because people can return to being productive members of their families, their workplace and our society.
Trials
involving women with advanced breast cancer also confirmed the benefits
of Herceptin®. A recent study showed that 3 years after
treatment, twice as many women with HER2 positive advanced breast cancer
who received Herceptin® and chemotherapy were alive than
those who were treated with chemotherapy alone.
Herceptin® is not currently government funded for women
with early-stage HER2 positive breast cancer but PHARMAC is currently
reviewing this. In the meantime, it costs approximately $60,000 to $100,000
per patient. For women with advanced breast cancer which is HER2 3+ or
FISH+, Herceptin® is already government funded in New
Zealand.
This
depends on a person’s response to treatment and/or the state of
the breast cancer. Standard Herceptin treatment duration for HER2
positive early breast cancer is 12 months.
Source: Breast
Cancer Aotearoa Coalition (BCAC) and the Infotorial by ADIS, entitled:
"Fact Sheet: Herceptin in the Treatment of Early Aggressive Breast
Cancer" (dated 5 February 2007).
Other Herceptin® information:
Herceptin® in Early Stage Breast Cancer - a Story in Progress
Breast Cancer
Network submission to Pharmac June 2008
BCAC
submission to Pharmac June 2008
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Committee
members and supporters at one of the many
Women's Challenge runs

Nic Russell and Claire Ryan

Group
who attended the
1st World Breast Cancer Conference in Canada