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November 19, 2008 |
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Name = Breast cancer | ICD10 = C50 | ICD9 = 174-175 | Breast cancer is cancer of breast tissue. Worldwide,it is the most common form of cancer in females, affecting approximately 10% of all woman|women at some stage of their life in the Western world. Although significant efforts are made to achieve early detection and effective treatment, about 20% of all women with breast cancer will die from the disease, and it is the second most common cause of cancer deaths in women. The risk of getting breast cancer increases with age. For a woman who lives to the age of 90 the odds of getting breast cancer her entire lifetime is about 12.5% or 1 in 8. Men can also develop breast cancer, but their risk is less than 1 in 1000 (see sex and illness). This risk is modified by many different factors. In a very small (~ 5%) proportion of breast cancer cases, there is a strong inherited familial risk. http://zmagsite.zmag.org/oct2002/commentary/albright1002.htm Some racial groups have a higher risk of developing breast cancer - notably, women of European and African descent have been noted to have a higher rate of breast cancer than women of Asian origin. (http://www.breastcancer.org/cmn_who_indrisk.html figures from breastcancer.org) However, these apparent racial differences diminish when geography is altered, as Asian women migrating to the western world, gradually acquire risk approaching that of western women. Other established risk factors include not having children, delaying first childbirth, not breastfeeding, early menarche (the first menstrual period), late menopause, obesity and taking hormone replacement therapy. The probability of breast cancer rises with age but breast cancer tends to be more aggressive when it occurs in younger women. One type of breast cancer that is especially aggressive and disproportionately occurs in younger women is inflammation|inflammatory breast cancer. It is initially staged as Stage IIIb or Stage IV. It also is unique because it often does not present with a lump so that it often is not detected by mammography or medical ultrasonography|ultrasound. It presents with the signs and symptoms of a breast infection like mastitis. Two genes, BRCA1 and BRCA2, have been linked to the rare familial form of breast cancer. Women in families expressing mutations in these genes have a much higher risk of developing breast cancer than women who do not. Together with Li-Fraumeni syndrome (p53 mutations), these genetic aberrations determine around 5% of all breast cancer cases, suggesting that the remainder is sporadic. Genetic counseling and genetic testing should be considered for families who may carry a hereditary form of cancer. Alcohol is another risk factor for the development of breast cancer. Women who drink half a glass of wine every day have 6% increased risk of developing breast cancer where as women who drink two drinks or more daily may have 37% increased chance of developing breast cancer. http://medicineworld.org/cancer/lead/8-2005/even-half-a-glass-of-wine-a-day-can-increase-the-risk-of-breast-cancer.html 1 The International Agency for Research on Cancer (IARC) in Lyon, France invited 21 scientist from 8 countries in June 2005, to evaluate the risk of cancer for humans of combined estrogen-progestogen contraceptives and combined estrogen-progestogen menopausal therapy. The Working Group found that there is a small increase in the relative risk of breast cancer in current and recent users of combined oral contraceptives. The risk decreases to that of never users ten years after cessation of use. The scientists described combined oral estrogen-progestogen contraceptives as ???carcinogenic to humans.??? They also found an increased risk of breast cancer in women under treatment with combined menopausal therapy, which is confined mostly to current or recent users, increases with duration of use and exceeds that in women taking estrogen-only therapy. The Working Group found that combined estrogen-progestogen menopausal therapy are "carcinogenic to humans." http://home.mdconsult.com/das/journal/view/49395500-2/N/15657385?ja=477482&PAGE=1.html&sid=391668990&source= Breast cancer, like other forms of cancer, is considered to be a result of damage to DNA. How this mechanism may occur comes from several known or hypothesized factors (such as exposure to ionizing radiation). Some factors lead to an increased rate of mutation (exposure to estrogens) and decreased repair (the BRCA1, BRCA2 and p53 genes). Although many epidemiological risk factors, and biological co-factors and promotors have been identified, the majority of breast cancer incidence remains unattributable, and the primary cause is unknown. Dietary influences have been proposed and examined, but these are small effects, and do not distinguish differences in risk within populations, as well as they do between populations. A significant environmental effect was revealed by the large difference in breast cancer incidence between countries and continents, and a migration effect which slowly increases the risk of breast cancer even across generations after migration from a country of lower incidence to a country of higher incidence, such as moving from China or Japan to the United States. Humans are not the only mammal prone to breast cancer. Some strains of mice, namely the house mouse (Mus domesticus) are prone to breast cancer which is caused by infection with the mouse mammary tumour virus (MMTV or "Bittner virus" for its discoverer Hans Bittner), by random insertional mutagenesis. Suspicion of MMTV or other viruses in human breast cancer is controversial, and the idea is not generally accepted for lack of direct and definitive evidence. There is much more research in diagnosis and treatment of breast cancer than in its cause. Due to the high incidence of breast cancer among older women, screening is now recommended in many countries. Screening methods suggested include breast self-examination and mammography. Only mammography has been proven to reduce mortality from breast cancer. In some countries routine (annual) mammography of older women is encouraged as a screening method to diagnose early breast cancer. Mammography is still the modality of choice for screening of early breast cancer. Magnetic resonance imaging (MRI) has been shown to detect cancers that are not visible on mammograms, but it has several disadvantages. For example, although it is more sensitive, it is less specific than mammography. It is also a relatively expensive procedure, and one which requires the injection of a chemical agent to be effective. It may be valuable for younger women, whose breasts contain less fat and more connective tissue, making it harder to spot cancers on mammograms. Medical ultrasonography|Ultrasound alone is not adequate as a screening tool but it is a useful additional investigation, especially for the characterisation of benign tumours. The U.S. National Cancer Institute recommends screening mammography with a baseline mammogram at age 35, mammograms every two years beginning at age 40, and then annual mammograms beginning at age 50. In the UK women are invited to attend for screening once every three years beginning at age 50. Women with a family history of breast cancer should start screening mammography at an earlier age, and it is usually suggested to start screening at an age that is 10 years less than the age at which a relative was diagnosed with breast cancer. Breast cancers detected by mammography are usually smaller than those detected clinically, and women who undergo mammography are more likely to be eligible for breast-conserving therapy. Many breast cancers are diagnosed now by mammography before they are large enough to be palpated, but despite screening efforts, many women are diagnosed with breast cancer after they notice a lump or when experiencing symptoms due to metastatic disease. Breast cancer can be suspected after a cautious clinical history, physical examination and imaging (either mammography or ultrasound). The diagnosis can only be established when a suspicious lump is biopsy|biopsied for histological confirmation of whether it is malignant or not. The biopsy is usually performed either with a fine needle guided by ultrasound or with a larger "core" needle. Some cases require an open biopsy after wire localization under x-ray. A pathology report will usually contain a description of histology|cell type and grade. Other useful information derived from the pathology laboratory include estrogen receptor and progesterone receptors status and HER2/neu status; these can help to guide treatment. The most common invasive breast cancer cell type is infiltrating ductal carcinoma. Other types include ductal carcinoma in situ (DCIS), lobular carcinoma in situ (LCIS), infiltrating lobular carcinoma, medullary carcinoma. After diagnosis, the next phase is tumour staging - this aims to assess the extent of the tumour and whether it has metastasis|metastasized (spread to distant sites). Staging For suspicious, high risk cases, other investigations which include CT scans, nuclear medicine studies (e.g. bone scans or PET imaging), magnetic resonance imaging (MRI), chest X-rays, and blood tests may be done to look for any metastasis or secondary cancer that has spread a long way from the site of the primary tumour. The standard way of categorising tumour is by Cancer staging|staging it using the TNM (Tumour, Nodes and Metastasis) system, which in turn determines treatment recommendations. The TNM system is specific for each type of cancer. Some biological features of the cancer such as estrogen receptor and HER2/neu oncogene expression are also determined as they also affect treatment recommendations. TNM classification The TNM classification of breast cancer:
Stage grouping
The cancer is staged depending on factors which include the size of the tumour, whether there is lymph node involvement or not and whether there is distant spread of cancer cells. Stages are a composite of the TNM. Stage I is small tumor (T1) without any spread, while stage IV is metastatic disease. Stages correlate with long-term prognosis, and treatment decisions are often made on the basis of the stage. The mainstay of breast cancer treatment is surgery when the tumor is localized, with possible adjuvant hormonal therapy (with tamoxifen or an aromatase inhibitor), chemotherapy, and/or radiotherapy. Surgery Depending on the staging and type of the tumour, just a lumpectomy (removal of the lump only) may be all that is necessary or removal of larger amounts of breast tissue may be necessary. Surgical removal of the entire breast is called mastectomy. Standard practice requires that the surgeon must establish that the tissue removed in the operation has margins clear of cancer, indicating that the cancer has been completely excised. If the tissue removed does not have clear margins, then further operations to remove more tissue may be necessary. This may sometimes require removal of part of the pectoralis major muscle which is the main muscle of the anterior chest wall. During the operation, the lymph nodes in the axilla are also considered for removal. In the past, large axillary operations took out 10-40 nodes to establish whether cancer had spread - this had the unfortunate side effect of frequently causing lymphedema of the arm on the same side as the removal of this many lymph nodes affected lymphatic drainage. More recently the technique of sentinel lymph node dissection has become popular as it requires the removal of far fewer lymph nodes, resulting in fewer side effects. Adjuvant therapy At present, the treatment recommendations after surgery (adjuvant therapy) follow a pattern. This pattern may be adapted as every two years a worldwide conference takes place in St. Gallen, Switzerland to discuss the actual results of worldwide multi-center studies. Depending on clinical criteria (age, type of cancer, size, metastasis) patients are roughly divided to high risk and low risk cases which follow different rules for therapy. The following list is a compilation of possibilities: #After a breast conserving therapy (lumpectomy, quadrant-resection), the high local recurrence risk (~40%) is reduced by radiation therapy to the breast #If the lymph nodes are positive, the high mortality risk (30-80%) is reduced by systemic treatment (either anti-hormones or chemotherapy). #In younger patients, the most useful systemic therapy is chemotherapy (usually older regimens such as CMF (therapy)|CMF, FAC, AC chemotherapy|AC and/or Taxol) and now the FDA approved regimen TAC (Taxotere, Adriamycin, Cytoxan) or FEC for 3 cycles followed by Taxotere for 3 cycles. Another standard regimen includes dose dense AC (Adriamycin and cyclophosphamide) followed by Taxol. This is given on a two week cycle with growth factor support, e.g. pegfilgrastim. #In older patients with estrogen receptor positive tumors, the most useful systemic therapy is anti-hormone therapy (tamoxifen, aromatase inhibitors, GnRH-analogues) #Chemotherapy has increasing side effects as the patient's age passes 65 #In patients with estrogen receptor negative tumours, the most useful systemic therapy is chemotherapy #In patients with estrogen receptor positive tumours, the most effective systemic therapy is hormone therapy with medications such as tamoxifen or an aromatase inhibitor (in postmenopausal women) #Two large clinical trials published in the summer of 2005 demonstrated that patients with positive nodes and HER2/neu positive breast cancer should be treated with trastuzumab (brand name Herceptin) in addition to traditional adjuvant chemotherapy An online resource for helping to quantify the relative risks and benefits of chemotherapy v. hormonal therapy is Adjuvant! Online (see below). Radiation therapy is recommended in all patients who had lumpectomy, however radiation therapy after mastectomy is recommended only if four or more lymph nodes are involved with cancer. Radiation therapy is usually not indicated in patients with advanced (stage IV disease) except for palliation of symptoms like bone pain. The emotional impact of cancer diagnosis, symptoms, treatment, and related issues can be severe. Most larger hospitals are associated with cancer support groups which can help patients cope with the many issues that come up in a supportive environment with other people with experience with similar issues. Online cancer support groups are also very beneficial to cancer patients, especially in dealing with uncertainty and body-image problems inherent in cancer treatment. There are several prognostic factors associated with breast cancer. Stage is the single most important prognostic factor in breast cancer, as it will take into consideration local involvement, lymphnode status and whether metastatic disease is present or not. The higher the stage at the time of diagnosis, the worse the prognosis of breast cancer is. Node negative breast cancer patients have a much better prognosis compared to node positive patients. Presence of estrogen and progesterone receptors in the cancer cell is another important prognostic factor, and may guide treatment. Hormone receptor positive breast cancer is usually associated with much better prognosis compared to hormone negative breast cancer. HER2/neu status has also been described as a prognostic factor. Patients whose cancer cells are positive for HER2/neu have more aggressive disease and may be treated with trastuzumab, a monoclonal antibody that targets this protein. Image:Pink ribbon.png|40px|right|Pink ribbon In the month of October, breast cancer is recognized by survivors, family and friends of survivors and/or victims of the disease. A pink awareness ribbon|ribbon is worn to recognize the struggle that men and women face when battling the cancer.
Category:Oncology Category:Gynecology Category:Types of cancer Category:Ribbon symbolism bg:?????? ???? ?????????????? de:Brustkrebs es:C??ncer de mama fr:Cancer du sein id:Kanker payudara it:Carcinoma mammario he:???????? ?????? ms:Penyakit barah payu dara nl:Borstkanker no:Brystkreft ja:?????? tr:Meme Kanseri vi:Ung th?? v?? This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Breast cancer".
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