One will often hear the words "HER-2 status" when a breast cancer lesion is being diagnosed and staged for treatment. The HER-2 (Her2/neu, c-erb-2 or erb-2) is a gene which produces a protein that acts as a receptor on the surface of cells. These receptors are very sensitive to hormonal/chemical 'growth' signals in the body, and are therefore 'growth factors'. If a cancer tumor has cells which seem to have more of these HER2 proteins than normal, that means those cells are receiving more 'messages' to grow and divide than normal cells. More specifically, HER-2/ neu, also known as c- erb B-2 (HER-2), is a a proto-oncogene located on chromosome 17. This gene is amplified therefore the protein (HER-2) overexpressed, in around 20-25% of invasive breast cancers.
Sometimes the phrase 'hormone receptor status' is used along with terms like 'protein status' and HER-2 status. These are all related terms; the presence of certain proteins is what makes a tumor more receptive to certain hormones. Some hormones effect growth rates, such as the hormones attracted by HER-2 proteins, but other hormones might suppress growth or be associated with healing and blood flow. The 'hormone receptor status' of a tumor is a composite of all the different proteins and associated hormones that might be influencing the behaviour a particular tumor in a particular patient, and the HER-2 status is a small subset of the overall hormonal picture, specifically related to the probable growth rate of the new cancer cells. HER-2 gene amplification in breast cancer has been associated with increased cell motility and cell proliferation, tumor invasiveness, accelerated angiogenesis, reduced apoptosis, and more progressive regional and distant metastases. So, breast cancers presenting with a higher-than-average or 'positive' HER-2 status will almost certainly be be more aggressive.
The most common way to measure the HER-2 status of a suspected breast cancer tumor is through an immunohistochemisty (IHC) test. This will likely be part of an overall histological/pathological evaluation of the tumor. Various tumor 'markers', including the HER-2 status indicators, give the pathogist a characterization of the tumor, which helps to predict its future behavior and probable responses to different types of treatments. The immunohistochesmistry test of the HER-2 status measures the 'over-expression' of a particular protein, and is typically given a 'score' of 0 to +3. (The pathologist will actually 'count' the number of receptors on the surface of the cancer cells, and can 'see' them microscopically because they are receptive to certain protein-based dyes, and change color.) Scores of 0 and +1 are considered indicative of a 'negative' status, while +2 and +3 are HER-2 positive. ( So, the test measures whether the HER2 proteins are overexpressed, or not. There is no 'in between' state.)
The other method of measuring the HER-2 status of a breast tumor is by fluorescent in situ hybridization (FISH), which measures the amplification of the HER-2 gene (the number of copies of the HER-2 gene present in a cancer cell). Like the immunohistochestry test, results of the FISH test are reported as either positive or negative.
The hormone-receptor status of a tumor is really considered to be more of a predictive factor rather than a 'prognostic' factor. It helps determine what you are up against, and how best to treat it. The outlook for a particular breast cancer is more likely to be influenced by the histological type and grade of the breast cancer tumor at the time it is discovered, and whether or not there is lymphatic involvement, and not the hormone receptor status. It is true, however, that breast cancer tumors with a positive hormone receptor status have a more 'indolent' course than do hormone receptor-negative tumors. Indolent is kind of a strange term to use, but it means that a tumor is less responsive or 'lazy' in terms of normal treatments than in tumors which the hormone receptor status is negative. Some kind of extra intervention or 'boost' is often required to really get a positive healing response from the cancer. But certain kinds of hormone-receptor positive tumors are actually more responsive to endocrine therapy, so there is a positive aspect to this as well. In fact there is often a kind of 'inverse' relationship between the HER-2 hormone receptor status, and the ER (estrogen receptor) and PR ( progesterone receptor) status of a tumor. Higher ER and PR hormone receptor levels in a tumor usually have a negative HER-2 status, and a good outlook, while breast cancers with a high or positive HER-2 expression will tend to have a low expression of ER and PR, and also a poorer prognosis.
Breast cancer tumors with a positive HER-2 status are usually fast growing and aggressive. There tends to be a higher level of HER-2 expression in higher grade tumors and in lower grade tumors. HER-2 receptors and also epidermal growth factor receptors are stimulants to cancer cell growth. Other hormonal factors of a tumor can also make the cancer more aggressive. Some breast cancer tumors will have decreased levels of tumor-suppressor genes ,such as p53, which make invasion beyond the breast ducts more likely. Decreased levels of metastasis-suppressor genes such as nm23 also make spread to the lymph nodes and other areas of the body more likely. HER-2 positive breast cancers do appear to be more likely to spread early in the cancer course to major visceral sites such as the axillary lymph nodes, lungs, bone marrow, liver, ovaries, and the adrenal glands.
There is also some evidence that HER-2 protein levels are significantly higher at the DCIS stage than in invasive-status breast cancers. The incidence of DCIS with HER-2 positivity ranges from about 24% to 38% in various studies, and that does appear to be a slightly higher rate than for invasive breast carcinoma. This suggests that HER-2 signalling might be an important factor in the early stages of breast tumorigenesis. Of interest, the rate of HER-2 overexpression in colloid (mucinous) breast cancer is actually extremely low, and also tends to be very low in tubular and medullary breast carcinoma.
Women with HER-2 positive breast cancer are usually offered treatment with trastuzumab (Herceptin Herceptin®), which is the only FDA-approved therapy for women with breast cancer tumors over-expressing HER-2 proteins. It is often the case that women with breast cancer tumors overexpressing HER-2 do not respond to tamoxifen (chemical/hormonal) therapy. But, the use of trastuzumab in combination with chemotherapy has lead to longer survival rates for women with metastatic HER-2 postive breast carcinomas. The addition of herceptin when HER-2 is positive gives an amazing boost to the response and cure rates. Herceptin is not really chemotherapy. Rather, it is a monoclonal antibody, and the use of cloned antibodies to combat breast cancer is sometimes referred to as 'biologic therapy'. Specifically, trastuzumab binds the extracellular portion of the HER-2 transmembrane receptor, and it was initially targeted for patients with advanced, relapsed breast cancer with overexpression of the HER-2 protein.
Sometimes HER-2 positive tumors are also treated with HER-2 targeting agents such as pertuzumab, ertumaxomab, HER-2 vaccines (which improve T-cell immunity in the context of HER-2 overexpression ) and tyrosine kinase inhibitors. Hormonal therapy, the use of anthracylines, and taxanes are also sometimes employed to minimize the growth-effect of HER-2 positive breast cancers. Since the rate of local recurrence is typically quite high with HER-2 postive tumors, radiation therapy is sometimes used in addition to trastuzumab-based neoadjuvant chemotherapy, and generally with good effect.
Many studies have demonstrated the overexpression of HER-2 proteins with a poorer prognosis. It is difficult however to isolate just the HER-2 aspect of the tumor as the specific cause of this poorer outlook, or to find practical indications of just what is meant by 'negative prognosis'. The HER-2 status is part of the picture, but so are tumor size and grade, lymph node status, other hormonal indicators ( for example, reduced levels of the tumor suppressor gene p53 make the prognosis worse), and the type of cancer involved. However it is clear that a positive HER-2 overexpression does correspond to an increased likelihood for lymph node metastasis. HER-2 overexpression can also predict a poorer response to taximophen (hormonal/chemical therapy), though researchers are working on ways to combat this.
What an overexpression of HER-2 really tends to accurately predict is the time to relapse (the disease free interval), and consequently the overall survival time is also predictably decreased. Some studies have shown that the median survival time for patients with HER-2 positive breast cancer is reduced by just over 50%. There are of course many factors that contribute to survival of breast cancer, but nonetheless, some studies have shown that only about 60% of patients with HER-2 positive status invasive breast cancer are disease free after 10 years, and about 65% survive overall (approx. 20 years or more). And, a greater number of HER-2 postive patients succumb to the illness during the first five years than those who are negative for HER-2 overexpression. At the same time, all other factors assumed to be equal, patients with negative HER-2 status tumors tend to be disease free at a rate of 75% over 10 years and have a slightly higher overall survival rate. From this we can informally estimate that women with breast cancer which overexpresses HER-2 are about 10% more likely to have significant difficulties and ultimately succumb to the disease within the first five years, than those who do not.