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Breast Cancer
Breast Cancer
Breast Cancer
Background
Worldwide, breast cancer is the most frequently diagnosed life-threatening cancer in women and the leading cause of cancer death among women. Many early breast carcinomas may be asymptomatic; pain or discomfort is not usually a symptom of breast cancer. Breast cancer is often first detected as an abnormality on a mammogram before it is felt by the patient or healthcare provider. The general approach to evaluation of breast cancer has become formalized as triple assessment: clinical examination, imaging (usually mammography and/or ultrasonography), and needle biopsy. (See Workup.) Increased public awareness and improved screening have led to earlier diagnosis, at stages amenable to complete surgical resection and curative therapies. Consequently, survival rates for breast cancer have improved significantly, particularly in younger women. Surgery is considered primary treatment for breast cancer. Many patients with early-stage breast cancer are cured with surgery alone. (See Treatment and Management.) Adjuvant treatment of breast cancer is designed to treat micrometastatic disease, or breast cancer cells that have escaped the breast and regional lymph nodes but which have not yet had an established identifiable metastasis. Depending on the model of risk reduction, adjuvant therapy has been estimated to be responsible for 35-72% of the reduction in mortality rate. Over the last 2 decades, breast cancer research has led to extraordinary progress in our understanding of the disease, resulting in more efficient and less toxic treatments. (See Treatment and Management.)
Anatomy
The breasts of an adult woman are milk-producing glands situated on the front of the chest wall. They rest on the pectoralis major muscle and are supported by and attached to the front of the chest wall on either side of the sternum by ligaments. Each breast contains 15-20 lobes arranged in a circular fashion. The fat that covers the lobes gives the breast its size and shape. Each lobe comprises many lobules, at the end of which are glands where milk is produced in response to hormones (see the image below).
Pathophysiology
The current understanding of breast tumorigenesis is that invasive cancers arise through a series of molecular alterations at the cellular level, resulting in the outgrowth and spread of breast epithelial cells with immortal features and uncontrolled growth. Genomic profiling has demonstrated the presence of discrete breast tumor subtypes with distinct clinical behavior (eg, 4 subclasses: luminal A, luminal B, basal, and human epidermal growth factor receptor 2 [HER2]-positive). The exact number of disease subtypes and molecular alterations from which these subtypes derive remains to be fully elucidated, but they generally align closely with the presence or absence of hormone receptor and mammary epithelial cell type (luminal or basal).
The figure below summarizes the current general understanding of breast tumor subtypes, prevalence, and the major associated molecular alterations. This view of breast cancer--not as a set of stochastic molecular events, but as a limited set of separable diseases of distinct molecular and cellular origins--has altered thinking about breast cancer etiology, type-specific risk factors, prevention, and treatment strategies.
Etiology
Epidemiologic studies have identified many risk factors that increase the chance of a woman developing breast cancer. Go to Breast Cancer Risk Factors for more information on this topic.
Epidemiology
Over the past 25 years, breast cancer incidence rates have risen globally, with the highest rates in Westernized countries. Reasons for this trend include change in reproductive patterns, increased screening, dietary changes, and decreased activity. Although breast cancer incidence is on the rise globally, breast cancer mortality has been decreasing, especially in industrialized countries. The 2002 international female breast cancer incidence rates varied by more than 25-fold, ranging from 3.9 cases per 100,000 in Mozambique to 101.1 cases per 100,000 in the United States. In 2008, the American Cancer Society (ACS) estimated there were nearly 1.4 million new cases of invasive breast cancer worldwide. In the US, approximately 207,090 new cases of female invasive breast cancer were predicted to occur in 2010, along with 1,970 cases in men.[1] In addition to invasive breast cancer, 54,010 new cases of in situ breast cancer were expected to occur among women, of which approximately 85% were expected to be ductal carcinoma in situ (DCIS). After 2 decades of increasing incidence rates, the number of new female breast cancers decreased by 2.2% per year from 1999 to 2005. This decrease is thought to reflect reduced use of HRT following the publication of the WHI findings in 2002, which linked HRT use to an increased risk of heart disease and breast cancer. Rates of DCIS have stabilized since 2000.[2] The current lifetime risk of breast cancer in the US is estimated at 12.7% for all women, 13.3% for non-Hispanic whites, and 9.98% for black women. Overall, the annual incidence rates in black women (119.4/100,000) and Hispanic/Latina women (89.9/100,000) have been stable since the early 1990s, and they are lower than the annual incidence of breast cancer in white women (141.1/100,000). However, black women are more likely than white women to be diagnosed with larger, advancedstage tumors (>5 cm). Although incidence rates among Asian and Pacific Islander women have continued to increase at 1.5% per year (89/100,000), they are still significantly lower than the rates in white women. Japanese and Taiwanese woman have one fifth the risk of US women.[3] The various types of breast cancers are listed below by percentage of cases: Infiltrating ductal carcinoma is the most commonly diagnosed breast tumor and has a tendency to metastasize via lymphatics; this lesion accounts for 75% of breast cancers Approximately 64,000 cases of DCIS are diagnosed annually in the US
Over the last 25 years, lobular carcinoma in situ (LCIS) incidence has doubled and is currently 2.8 per 100,000 women; the peak incidence is in women aged 40-50 years Infiltrating lobular carcinoma comprises less than 15% of invasive breast cancers Medullary carcinoma accounts for about 5% of cases and generally occurs in younger women Mucinous (colloid) carcinoma is seen in fewer than 5% of invasive breast cancer cases. Tubular carcinoma of the breast is comprises 1-2% of all breast cancers Papillary carcinoma is usually seen in women older than 60 years and accounts for approximately 12% of all breast cancers Metaplastic breast cancer accounts for less than 1% of breast cancer cases, tends to occur in older women (average age of onset in the sixth decade), and has a higher incidence in blacks Mammary Paget disease comprises 1-4% of all breast cancers and has a peak incidence in the sixth decade of life (mean age, 57 y)
Prognosis
Death rates from breast cancer in the United States have decreased steadily in women since 1990. The breast cancer mortality rate fell 24% between the years 1990 and 2000 for women aged 30-79 years. The largest decrease in mortality has been seen in women younger than 50 years (3.3% per year) compared with those aged 50 years and older (2.0% per year). The decrease in breast cancer death rates is thought to represent progress in both earlier detection and improved treatment modalities.[1] The 2010 estimates were 40,230 expected breast cancer deaths (39,840 women, 390 men).[1]
Stage 0: 99-100% Stage I: 95-100% Stage II: 86% Stage III: 57% Stage IV: 20% This prognostic information can guide physicians in making therapeutic decisions. Pathologic review of the tumor tissue for histological grade along with the determination of estrogen/progesterone receptor status and HER2 status is necessary for determining prognosis. Evaluation of lymph node involvement by sentinel lymph node biopsy or axillary lymph node dissection is generally[18]necessary as well. (See Staging.)
HER2
Before the routine use of trastuzumab (Herceptin, a monoclonal antibody) in adjuvant therapy, HER2 overexpression was associated with a more aggressive tumor phenotype and worse prognosis (higher rate of recurrence and mortality), independent of other clinical features (eg, age, stage, tumor grade), especially in patients who did not receive adjuvant chemotherapy. Additionally, HER2 status has been shown to be predictive for response to certain chemotherapeutic agents (ie, doxorubicin [Adriamycin]; and HER2-targeted therapies trastuzumab and lapatinib [Tykerb, a small-molecule oral tyrosine kinase inhibitor directed specifically to the HER2 receptor]). Retrospectively analyzed results from clinical trials have shown that HER2-positive patients benefit from anthracycline-based regimens secondary to the coamplification of topoisomerase II with HER2. Preliminary data also suggest that HER2 may predict response to and benefit from paclitaxel in the adjuvant setting. Go to Breast Cancer and HER2 for complete information on this topic.
Infiltrating ductal carcinoma is the most commonly diagnosed breast tumor and has a tendency to metastasize via lymphatics.
Medullary carcinoma
Roughly 30% of patients have lymph node metastasis. Typical or classic medullary carcinomas are often associated with a good prognosis despite the unfavorable prognostic features associated with this type of breast cancer. However, an analysis of 609 medullary breast cancer specimens from various stage I and II National Surgical Adjuvant Breast and Bowel Project (NSABP) protocols indicates that overall survival and prognosis are not as good as previously reported.
Mucinous carcinoma
Overall, patients with mucinous carcinoma have an excellent prognosis, with a greater than 80% 10year survival.
Tubular carcinoma
This type of breast cancer has a low incidence of lymph node involvement and a very high overall survival rate. Because of its favorable prognosis, patients are often treated with only breastconserving surgery and local radiation therapy.
Papillary carcinoma
Cystic papillary carcinoma has a low mitotic activity, which results in a more indolent course and good prognosis. However, invasive micropapillary ductal carcinoma has a more aggressive phenotype, even though approximately 70% of cases are ER-positive. A retrospective review of 1,400 cases of invasive carcinoma identified 83 cases (6%) with at least one component of invasive micropapillary ductal carcinoma. Additionally, lymph node metastasis is seen frequently in this subtype (70-90% incidence), and the number of lymph nodes involved appears to correlate with survival.
Patient Education
For patient education information, see eMedicine's Cancer and Tumors Center,Women's Health Center, and Imaging Center, as well as Breast Cancer,Mastectomy, Breast Lumps and Pain, Breast Self-Exam, Mammogram, andOvarian Cancer.
History
Many early breast carcinomas are asymptomatic, particularly if they were discovered during a breastscreening program. Larger tumors may present as a painless mass. Pain or discomfort is not usually a symptom of breast cancer; only 5% of patients with a malignant mass present with breast pain.
Often, the purpose of the history is not diagnosis but risk assessment. A family history of breast cancer in a first-degree relative is the most widely recognized breast cancer risk factor. The lifetime risk is up to 4 times higher if a mother and sister are affected; the risk is approximately 5 times greater in women with 2 or more first-degree relatives with breast cancer; and it is also greater among women with breast cancer in a single first-degree relative, particularly if the relative was diagnosed at an early age (50 y or younger). A family history of ovarian cancer in a first-degree relative, especially if the disease occurred at an early age (< 50 y), has been associated with a doubling of breast cancer risk. The family history characteristics that suggest increased risk of cancer are summarized as follows: Two or more relatives with breast or ovarian cancer Breast cancer occurring in an affected relative younger than 50 years Relatives with both breast cancer and ovarian cancer One or more relatives with 2 cancers (breast and ovarian cancer or 2 independent breast cancers) Male relatives with breast cancer BRCA1 and BRCA2 mutations Ataxia telangiectasia heterozygotes (4-times increased risk) Ashkenazi Jewish descent (2-times greater risk) Neoplastic conditions that increase the risk of breast cancer include the following: Previous breast cancer Ovarian cancer Endometrial cancer Ductal carcinoma in situ (DCIS) Lobular carcinoma in situ (LCIS) Benign breast conditions that increase the risk of breast cancer include the following: Hyperplasia (unless mild) Complex fibroadenoma Radial scar Papillomatosis Sclerosing adenosis Microglandular adenosis Cervical cancer is associated with a decreased risk of breast cancer.
Physical Examination
If the patient has not noticed a lump, then signs and symptoms indicating the possible presence of breast cancer may include the following: Change in breast size or shape Skin dimpling or skin changes (eg, thickening, swelling, redness) Recent nipple inversion or skin change, or nipple abnormalities (eg, ulceration, retraction, spontaneous bloody discharge) Single-duct discharge, particularly if bloodstained Axillary lump To detect subtle changes in breast contour and skin tethering, the examination must include an assessment of the breasts with the patient upright with arms raised. The following findings should raise concern: Lump or contour change Skin tethering Nipple inversion Dilated veins Ulceration Paget disease Edema or peau d'orange
The nature of palpable lumps is often difficult to determine clinically, but the following features should raise concern: Hardness Irregularity Focal nodularity Asymmetry with the other breast Fixation to skin or muscle (assess fixation to muscle by moving the lump in the line of the pectoral muscle fibers with the patient bracing her arms against her hips) A complete examination includes assessment of the axillae and supraclavicular fossae, examination of the chest and sites of skeletal pain, and an abdominal and neurologic examination. The clinician should be alert to symptoms of metastatic spread, such as the following: Breathing difficulties Bone pain Symptoms of hypercalcemia Abdominal distention Jaundice Localizing neurologic signs Altered cognitive function The clinical evaluation should include a thorough assessment of specific risk factors for breast cancer. Go to Breast Cancer Risk Factors for more information on this topic.
Diagnostic Considerations
The differential diagnosis includes the following: Circumscribed breast lesions: benign breast disease (eg, fibroadenomas, cysts), breast cancer, breast lymphoma, and metastasis to the breast from other primary sites Skin thickening: inflammatory carcinoma and mastitis Stellate lesions: breast cancer, traumatic fat necrosis, a radial scar, and a hyalinized fibroadenoma Dilated ducts with or without nipple discharge: papilloma, ductal carcinoma, duct ectasia, and fibrocystic disease
Differential Diagnoses
Breast Abscess and Masses Breast, Fibroadenoma
Approach Considerations
Breast cancer evaluation should be approached with an ordered inquiry beginning with symptoms and general clinical history, followed by clinical examination and, finally, investigation, which may include imaging and biopsy. This approach naturally lends itself to a gradually increasing degree of invasiveness, so that a diagnosis can be obtained with the minimum amount of invasion and, consequently, minimum discomfort to the patient. Because the more invasive investigations also tend to be the most expensive, this approach is usually the most economical. The aims of evaluation of a breast lesion are to judge whether surgery is required and, if so, to plan the most appropriate surgery. The ultimate goal of surgery is to achieve the most appropriate degree of breast conservation while minimizing the need for reoperation. The general approach to evaluation of breast cancer has become formalized as triple assessment: clinical examination, imaging (usually mammography and/or ultrasonography), and needle biopsy. However, this should always be performed as part of a more general assessment beginning with clinical history. Breast cancer is often first detected as an abnormality on a mammogram before it is felt by the patient or healthcare provider. Mammographic features suggestive of malignancy include asymmetry, microcalcifications, a mass, or architectural distortion. If any of these features are identified, a diagnostic mammogram along with a breast ultrasound should be performed before obtaining a biopsy. In certain cases, breast magnetic resonance imaging (MRI) may be warranted.
Mammography
Mammography is a special type of low-dose x-ray imaging used to create detailed images of the breast. Mammography can demonstrate microcalcifications smaller than 100 m; it often reveals a lesion before it is palpable by CBE and, on average, 1-2 years before noted by BSE. There are 2 types of mammography examinations: screening and diagnostic. Screening mammography is done in asymptomatic women. Diagnostic mammography is performed in symptomatic women (eg, when a breast lump or nipple discharge is found during self-examination or an abnormality is found during screening mammography). This examination is more involved, time-consuming, and expensive than screening mammography and is used to determine the exact size and location of breast abnormalities and to image the surrounding tissue and lymph nodes. Women with breast implants or a personal history of breast cancer will usually require the additional views used in diagnostic mammography.
Ultrasonography
Ultrasonography has become a widely available and useful adjunct to mammography in the clinical setting. Ultrasound is generally used to assist the clinical examination of a suspicious lesion detected on mammography or physical examination. As a screening device, ultrasound is limited by a number of factors, most notably by the failure to detect microcalcifications and by poor specificity (34%). Originally, ultrasonography was used primarily as a relatively inexpensive and effective method of differentiating cystic breast masses, which did not require sampling, from solid breast masses that were usually examined with biopsy; in many cases, the results of these biopsies were benign. However, it is now well established that ultrasonography also provides valuable information about the nature and extent of solid masses and other breast lesions. This imaging technique is also useful in the guidance of biopsies and therapeutic procedures; research is currently under way to evaluate its role in cancer screening.
Detection of occult breast carcinoma in a patient with carcinoma in an axillary lymph node Evaluation of suspected multifocal or bilateral tumor Evaluation of invasive lobular carcinoma, which has a high incidence of multifocality Evaluation of suspected, extensive, high-grade intraductal carcinoma Detection of occult primary breast carcinoma in the presence of metastatic adenocarcinoma of unknown origin Monitoring of the response to neoadjuvant chemotherapy Detection of recurrent breast cancer
Contraindications to MRI
Conversely, in a number of situations, MRI is essentially contraindicated, usually because of physical constraints that prevent adequate patient positioning. These constraints include the following: Contraindication to gadolinium-based contrast media (eg, allergy, pregnancy) Patient's inability to lie prone Marked kyphosis or kyphoscoliosis Marked obesity Extremely large breasts Severe claustrophobia Relative contraindications also exist. These are essentially based on the high sensitivity but limited specificity of the technique. MRI may not be useful for the following: Cancer-phobic patients Assessment of mammographically detected microcalcifications
Nuclear Imaging
Three radiotracers are commonly used for breast imaging or scintimammography in either clinical practice or research: technetium-99m (99m Tc)-sestamibi and99mTc-tetrofosmin (both used for myocardial perfusion imaging), as well as99m Tc-methylene diphosphonate (MDP) (used for bone scintigraphy).99m Tc-sestamibi was the first radiopharmaceutical agent to be approved by the FDA for use in scintimammography.[4] Although not indicated as a screening procedure for the detection of breast cancer, scintimammography may play a useful and significant role in various specific clinical indications, as in cases of nondiagnostic or difficult mammography and in the evaluation of high-risk patients, tumor response to chemotherapy, and metastatic involvement of axillary lymph nodes. In several prospective studies, overall sensitivity of 99m Tc-sestamibi scintimammography in the detection of breast cancer was 85%, specificity was 89%, and positive and negative predictive values were 89% and 84%, respectively. Similar numbers have been demonstrated for 99m Tc-tetrofosmin and99m Tc-MDP scintimammography.[4]
Modality
Sensitivity
Specificity
Indications
Mammography
63-95%
14-90%
Initial investigation for symptomatic breast in women older than 35 years and for screening; investigation of choice for microcalcification
(>95% palpable,
(90% palpable)
(94% palpable)
50% impalpable,
Ultrasonography
68-97% (palpable)
74-94% (palpable)
92% (palpable)
MRI
86-100%
21-97%
52%
Scarred breast, implants, multifocal lesions, and borderline lesions for breast conservation; may be useful in screening high-risk women
Scintigraphy
76-95% (palpable)
62-94%
70-83%
Lesions larger than 1 cm and axilla assessment; may help predict drug resistance
52-91% (impalpable)
(94% impalpable)
(83% palpable,
79% impalpable)
PET scanning
96%
100%
Breast Biopsy
Percutaneous vacuum-assisted large-gauge core biopsy (VACNB) with image guidance is the recommended diagnostic approach for newly diagnosed breast cancers. Core biopsies spare the need for operative intervention (and subsequent scarring), often providing pathologic results more quickly than surgical excisions. Additionally, excisional biopsy, as the initial operative approach, has been shown to increase the rate of positive margins. Thus, core biopsies for diagnosing breast cancer can eliminate the need for additional surgeries for definitive margin control and assessment of nodal status. The ultimate diagnostic biopsy is open excisional biopsy of a lesion, normally performed under general anesthesia. Open excisional biopsy should be reserved for lesions where the diagnosis remains equivocal despite imaging and less invasive assessment, or the procedure should be used for benign lesions that the patient chooses to have removed. A wide clearance of the lesion is usually not the goal in diagnostic biopsies, thus avoiding unnecessary distortion of the breast. Ongoing audit is essential to help reduce an excessive benign-to-malignant biopsy ratio.
Histology
Breast cancers usually are epithelial tumors of ductal or lobular origin (see the images below). The following features are all important in deciding on a course of treatment for any breast tumor: Size Status of surgical margin Presence or absence of estrogen receptors and progesterone receptors Nuclear and histologic grade DNA content S-phase fraction Vascular invasion Tumor necrosis Quantity of intraductal component
Histologic grade
Histologic grade is the best predictor of disease prognosis in carcinoma in situ, but it is dependent on the grading system used, such as the Van Nuys classification (high-grade, low-grade comedo, lowgrade noncomedo). The grading of invasive carcinoma is also important as a prognostic indicator, with higher grades indicating a worse prognosis. Grade I tumors are associated with a 10-year survival rate of 85%, whereas the survival rate falls to 45% for grade III tumors. Microscopic criteria for grading are shown in Table 3, below. Table 3. Grading System in Invasive Breast Cancer (Modified Bloom and Richardson) (Open Table in a new window)
Score 1 A. Tubule formation B. Mitotic count per high-power field >75% <7 2 10-75% 7-12 3 < 10% >12
Near normal
Slightly enlarged
Markedly enlarged
Little variation
Moderate variation
Marked variation
Grade I cancer if the total score (A + B + C) is 3-5 Grade II cancer if the total score (A + B + C) is 6 or 7
Breast cancer. Intraductal carcinoma, comedo type. Distended duct with intact
basement membrane and central tumor necrosis. Breast cancer. Intraductal carcinoma, noncomedo type. Distended duct with intact basement membrane, micropapillary, and early cribriform growth pattern.
Table 4. Ductal Carcinoma in Situ Subtypes (Open Table in a new window) DCIS Characteristic Comedo Nuclear grade Estrogen receptor High Negative Noncomedo Low Positive Absent
with monotonous population of neoplastic cells. Breast cancer. Lobular carcinoma in situ. Enlargement and expansion of lobule with monotonous population of neoplastic cells.
Breast cancer. Infiltrating ductal carcinoma. Low-grade carcinoma with welldeveloped glands invading the fibrous stroma.
Medullary carcinoma
Medullary carcinoma is relatively uncommon (5%) and generally occurs in younger women. Most patients present with a bulky palpable mass with axillary lymphadenopathy. Diagnosis of this type of breast cancer depends on the following histologic triad: 1. Sheets of anaplastic tumor cells with scant stroma 2. Moderate or marked stromal lymphoid infiltrate 3. Histologic circumscription or a pushing border DCIS may be observed in the surrounding normal tissues. ER, PR, and HER2 are typically negative, and TP53 is commonly mutated.
Mucinous carcinoma
Mucinous (colloid) carcinoma is another rare histologic type seen in fewer than 5% of invasive breast cancer cases. It usually presents during the seventh decade of life as a palpable mass or appears mammographically as a poorly defined tumor with rare calcifications.
Mucin production is the histologic hallmark with 2 main forms, type A and B, with AB lesions possessing features of both. Type A mucinous carcinoma represents the classic variety with larger quantities of extracellular mucin (see the following image), whereas type B is a distinct variant with endocrine differentiation. DCIS is not a frequent occurrence, although it may be found. Most cases are ER- and PR-positive, but HER2 overexpression is rare. Additionally, these carcinomas predominantly express glycoproteins MUC2 and MUC6. Overall, patients with mucinous carcinoma have an excellent prognosis (>80% 10year survival).
Breast cancer. Colloid (mucinous) carcinoma. Nests of tumor cells in pool of extracellular mucin.
Tubular carcinoma
Tubular carcinoma of the breast is an uncommon histologic type involving 1-2% of all breast cancers. Characteristic features of this type include a single layer of epithelial cells with low-grade nuclei and apical cytoplasmic snoutings arranged in well-formed tubules and glands. Tubular components comprise more than 90% of pure tubular carcinomas and at least 75% of mixed tubular carcinomas. This type of breast cancer has a low incidence of lymph node involvement and a very high overall survival rate. Because of its favorable prognosis, patients are often treated with only breast-conserving surgery and local radiation therapy.
Papillary carcinoma
Papillary carcinoma of the breast encompasses a spectrum of histologic subtypes (see the image below). There are 2 common types: cystic (noninvasive form) and micropapillary ductal carcinoma (invasive form). This form of breast cancer is usually seen in women older than 60 years and accounts for approximately 1-2% of all breast cancers. Papillary carcinomas are centrally located in the breast and can present as bloody nipple discharge. They are strongly ER- and PR-positive. Cystic papillary carcinoma has a low mitotic activity, which results in a more indolent course and good prognosis. However, invasive micropapillary ductal carcinoma has a more aggressive phenotype, even though approximately 70% of cases are ER-positive. A retrospective review of 1,400 cases of invasive carcinoma identified 83 cases (6%) with at least one component of invasive micropapillary ductal carcinoma. Additionally, lymph node metastasis is seen frequently in this subtype (70-90% incidence), and the number of lymph nodes involved appears to correlate with survival.
Breast cancer. Papillary carcinoma. Solid papillary growth pattern with early cribriform and well-developed thin papillary fronds.
A wide variety of histologic patterns includes the following: Spindle-cell carcinoma Carcinosarcoma Squamous cell carcinoma of ductal origin Adenosquamous carcinoma Carcinoma with pseudosarcomatous metaplasia Matrix-producing carcinoma This diverse group of malignancies is identified as a single entity based on a similarity in clinical behavior. When compared with infiltrating ductal carcinoma, MBC tumors are larger; more rapidly growing; commonly node-negative; and typically ER-, PR-, and HER2-negative.
Staging
The American Joint Committee on Cancer (AJCC) staging system groups patients into 4 stages based on tumor size (T), lymph node status (N), and distant metastasis (M). See Table 5, below.
N2: Metastasis in ipsilateral axillary lymph node(s) fixed or matted, or in clinically apparent ipsilateral internal mammary nodes in the absence of clinically evident axillary lymph node metastasis N2a: Metastasis in ipsilateral axillary lymph nodes fixed to one another or to other structures N2b: Metastasis only in clinically apparent ipsilateral internal mammary nodes and in the absence of clinically evident axillary lymph nodes N3: Metastasis in ipsilateral infraclavicular or supraclavicular lymph node(s) with or without axillary lymph node involvement, or clinically apparent ipsilateral internal mammary lymph node(s) and in the presence of axillary lymph node N3a: Metastasis in ipsilateral infraclavicular lymph node(s) N3b: Metastasis in ipsilateral internal mammary lymph node(s) and axillary lymph node(s) N3c: Metastasis in ipsilateral supraclavicular lymph node(s)
Distant metastasis
Metastases are defined as follows: Mx: Distant metastasis cannot be assessed M0: No distant metastasis M1: Distant metastasis Table 5. TNM Staging System for Breast Cancer (Open Table in a new window) Stage Stage 0 Stage I Stage IIA Tumor Node Tis T1 T0 N0 N0 N1 Metastases M0 M0 M0
T1
N1
M0
T2
N0
M0
Stage IIB
T2
N1
M0
T3
N0
M0
Stage IIIA T0
N2
M0
T1
N2
M0
T2
N2
M0
T3
N1-2
M0
Stage IIIB T4
N0
M0
T4
N1
M0
T4
N2
M0
N3
M0
Any N M1
Five-year survival rates are highly correlated with tumor stage, as follows: Stage 0: 99-100% Stage I: 95-100% Stage II: 86% Stage III: 57% Stage IV: 20% This prognostic information can guide physicians in making therapeutic decisions. Pathologic review of the tumor tissue for histological grade along with the determination of estrogen/progesterone receptor status and HER2 status is necessary for determining prognosis. Evaluation of lymph node involvement by sentinel lymph node biopsy or axillary lymph node dissection has also been considered necessary for staging and prognosis, as recommended in the 2009 edition of the National Comprehensive Cancer Network (NCCN) breast cancer guidelines, but the 2011 update modifies this recommendation. The 2011 NCCN breast cancer guidelines state that lymph node evaluation is optional in the following cases: Strongly favorable tumors When no result would affect the choice of adjuvant systemic therapy Elderly patients Patients with comorbid conditions The 2011 NCCN guidelines state that for staging, sentinel lymph node biopsy is preferred over axillary lymph node dissection.[6, 18] .
Additional Testing
The 2011 NCCN guidelines, like the 2009 version, recommends the following laboratory studies for all asymptomatic women with early-stage breast cancer (stages I and II): Complete blood cell (CBC) count with differential Liver function tests (LFTs) Renal function tests Serum calcium In addition, women with stage III (locally advanced or inflammatory breast cancer) or symptomatic disease should have a chest x-ray or CT scan of the chest, CT scan of the abdomen and pelvis, and bone scan for evaluation of distant metastasis. Tumor markers (carcinoembryonic antigen [CEA] and CA15.3 or CA27.29) may also be obtained in these patients.[6, 18]
Genetic testing for BRCA1 and BRCA2 can be performed in selected high-risk patients with a strong family history of breast or ovarian carcinoma. However, genetic counseling and discussion of subsequent management and treatment options should be performed before testing.
HER2 testing
Although several methods for HER2 testing have been developed, approximately 20% of current HER2 testing may be inaccurate; therefore, the American Society of Clinical Oncology (ASCO) and CAP have recommended guidelines in HER2 testing to ensure accuracy. Breast cancer specimens should initially undergo HER2 testing by a validated immunohistochemistry (IHC) assay (ie, HercepTest, Dako, Glostrup, Denmark) for HER2 protein expression.[7] The scoring method for HER2 expression is based on the cell membrane staining pattern and is as follows: 3+: Positive HER2 expression - Uniform intense membrane staining of more than 30% of invasive tumor cells 2+: Equivocal for HER2 protein expression - Complete membrane staining that is either nonuniform or weak in intensity but has circumferential distribution in at least 10% of cells 0 or 1+: Negative for HER2 protein expression Breast cancer specimens with equivocal IHC should undergo validation using aHER2 gene amplification method, such as fluorescence in situ hybridization (FISH). More centers are relying on FISH alone for determining HER2 status. In general, FISH testing is thought to be more reliable than IHC, but it is more expensive. Equivocal IHC results can be seen in 15% of invasive breast cancers, whereas equivocal HER2 FISH results are seen in less than 3% of invasive breast cancer specimens and those that had previously been considered HER2 positive. Discordant results (IHC 3+/FISH negative or IHC less than 3+/FISH positive) have been observed in approximately 4% of specimens. Currently, no data support excluding this group from treatment with trastuzumab. Newer methodologies for establishing HER2 status, including reverse transcriptasepolymerase chain reaction (RT-PCR) and chromogenic in situ hybridization (CISH), have not yet been validated. The interpretation for HER2 FISH testing (HER2/CEP17 ratio and gene copy number) is given below: Positive HER2 amplification: FISH ratio is greater than 2.2 or HER2 gene copy is greater than 6.0 Equivocal HER2 amplification: FISH ratio of 1.8-2.2 or HER2 gene copy of 4.0-6.0 Negative HER2 amplification: FISH ratio is less than 1.8 or HER2 gene copy of less than 4.0 Go to Breast Cancer and HER2 for complete information on this topic.
Oncotype Dx assay
The Onco type Dx assay (Genomic Health, Inc, Redwood City, Calif) has been validated in and approved by the FDA for women with early-stage, ER-positive, node-negative breast cancer treated with tamoxifen, where the recurrence score (RS) correlated with both relapse-free interval and overall survival. This assay is an RT-PCR-based assay of 21 genes (16 cancer genes and 5 reference genes) performed on paraffin-embedded breast tumor tissue. Using a formula based on the expression of these genes, a recurrence score can be calculated that correlates with the likelihood of distant recurrence at 10 years. Breast tumors with a recurrence score of less than 18 are considered low risk; a score of 18-30 is considered intermediate risk; and a score greater than 30 is considered high risk. Furthermore, the Onco type Dx assay has been shown retrospectively in the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-14 and B-20 studies to predict benefit from chemotherapy and hormonal therapy in hormone-sensitive, node-negative tumors. Women with a low recurrence score showed a significantly greater improvement in disease-free survival (DFS) with the addition of tamoxifen versus chemotherapy, whereas women with a high recurrence score had a significant improvement in disease-free survival with the addition of chemotherapy. Among women with 1-3 node-positive, hormone receptor-positive disease, the Onco type Dx recurrence score was a significant predictor of recurrence, with a 21% decrease in recurrence risk for each 10-point drop in the recurrence score.
In general, results from these studies would indicate that a select group of node-positive, hormone receptor-positive patients with a low recurrence score would not benefit from an anthracycline-based regimen. The benefit of adding chemotherapy to hormonal therapy in tumors with an intermediate score is still controversial; The Trial Assigning Individualized Options for Treatment [TAILORx] Trial, a large, prospective, randomized phase III study sponsored by the National Cancer Institute (NCI), is addressing this important question.
pproach Considerations
Surgery is considered primary treatment for breast cancer, as many patients with early-stage disease are cured with surgery alone. The goals of breast cancer surgery include complete resection of the primary tumor with negative margins to reduce the risk of local recurrences, and pathologic staging of the tumor and axillary lymph nodes for providing necessary prognostic information. Several different types of operations are available for the treatment of breast cancer. Adjuvant treatment for breast cancer involves radiation therapy and a variety of chemotherapeutic and biologic agents.
breast. Mirror biopsy of the contralateral breast, once advocated in the treatment of LCIS, is mainly of historic interest.
LABC encompasses both relatively indolent neglected tumors and those that have grown rapidly as a result of their inherent biology. It is as heterogeneous as invasive breast cancer in general, and, in most case series, LABC has a better long-term outcome than IBC, even when only inoperable cases are considered.
P2) showed that tamoxifen reduced the risk of DCIS and invasive breast cancer by 30-50%. In the NSABP P2 prevention trial, raloxifene was as effective as tamoxifen in reducing the risk of invasive breast cancer but was 30% less effective than tamoxifen in reducing the risk of DCIS. ACOG has updated its practice guidelines regarding pharmacologic intervention (eg, tamoxifen, raloxifene, aromatase inhibition) for breast cancer risk reduction. [10] Some of the highlights of the expert panel's literature review are as follows: Tamoxifen use for 5 years reduces risk of breast cancer for at least 10 years in premenopausal women, particularly ER-positive invasive tumors. Women 50 years or younger have few adverse effects with tamoxifen, and vascular/vasomotor adverse effects do not persist post treatment. Tamoxifen and raloxifene are equally effective in reducing risk of ER-positive breast cancer in postmenopausal women. Raloxifene is associated with lower rates of thromboembolic disease, benign uterine conditions, and cataracts than tamoxifen. Evidence does not exist on whether either agent decreases mortality from breast cancer. Recommendations include the following: For women with increased risk for breast cancer, offer tamoxifen (20 mg/d for 5 y) to reduce the risk of invasive ER-positive breast cancer In postmenopausal women, raloxifene (60 mg/d for 5 y) may also be considered Aromatase inhibitors (eg, anastrozole, exemestane, letrozole), fenretinide, or other SERMs are not recommended for use outside of a clinical trial
Long-term Monitoring
Follow-up guidelines
There is no consensus among oncologists as to the appropriate and optimal follow-up for long-term breast cancer survivors. The majority of relapses, both local and distant, occur within the first 3 years, especially in higher risk and ER-negative patients. The 2007 ASCO guidelines do not support the use of tumor biomarkers, including CEA, CA15.3, and CA27.29, for monitoring patients for recurrence after primary breast cancer therapy. Table 6, below, lists the NCCNs recommendations for breast cancer patients in the adjuvant setting. Table 6. Follow-up Recommendations for Breast Cancer Survivors per NCCN Guidelines (Open Table in a new window)
Intervention* History and physical examination Year 1 q3-4 mo Year 2 q4 mo Year 3-5 q6 mo Year 6+ Annually
Mammography
Annually
Annually
Annually
post-BCS irradiation)
NR
NR
NR
NR
Annually q1-2 y
Annually
Annually
Annually
Bone scan, blood counts, LFTs, and tumor markers are not routinely recommended
Postsurgical imaging
Women who have had surgery for breast cancer may still require breast cancer screening with mammography. If a woman had a total mastectomy, then the other breast requires yearly follow-up, because she is still at higher risk of developing cancer in the remaining breast. If she had subcutaneous mastectomy, partial mastectomy, or lumpectomy, then that breast itself requires followup mammography. The first mammogram is best performed 6 months postoperatively to provide a baseline for the new postoperative and radiation changes. Thereafter, mammography may be performed every 6-12 months for screening and follow-up. Go to Postsurgical Breast Imaging for more information on this topic. Monitoring of metastatic disease Recommendations for monitoring disease response in the metastatic setting vary. In general, monthly evaluations consisting of a history and physical examination to evaluate progression of disease and toxicities are reasonable. Tumor markers, such as CEA, CA15.3, and CA27.29, can be used in conjunction with diagnostic imaging, history, and physical examination for monitoring while on active therapy. CA15.3 and CA27.29 levels correlate with the course of disease in 60-70% of patients, whereas CEA levels correlate in 40% of patients. However, data are insufficient to recommend the use of CEA, CA15.3, or CA27.29 alone for monitoring response to treatment. Caution should be used when interpreting rising CEA, CA15.3, or CA27.29 levels during the first 4-6 weeks of a new therapy, as spurious early rises may occur. Standardized guidelines for imaging are not yet established and should be tailored to each patient. In general, CT scanning (chest, abdomen, and pelvis), MRI, bone scanning, or PET/CT scanning are performed when symptoms change or tumor markers rise. Circulating tumor cells are cells present in the blood that possess antigenic or genetic characteristics similar to a primary tumor type. The FDA has recently approved the CellSearch System (Veridex, Raritan, NJ) for the detection of circulating tumor cells in patients with metastatic breast cancer. This system captures circulating tumor cells using an immunomagnetic process with an epithelial cell adhesion molecule coated with magnetic beads and cytokeratin antibodies. A circulating tumor cell is identified when it is cytokeratin- and DAPI-positive but CD45-negative. Studies done by Cristofanilli using the CellSearch System have shown a prognostic utility and predictive use for circulating tumor cells in metastatic breast cancer patients. [11] Circulating tumor cell positive patients (>5 CTCs/7.5 mL blood) were shown to have a worse progression-free survival (17%) and overall survival than the circulating tumor cellnegative patients (36%). The presence of more than 5 circulating tumor cells before hormonal or chemotherapy treatment and following the first cycle of treatment also predict a worse outcome. However, studies to date have used small sample sizes, and no data have shown that use of circulating tumor cell testing affects overall survival or improves on quality of life. Per ASCO guidelines, the use of circulating tumor cell testing in breast cancer is not recommended for the diagnosis of breast cancer, nor should test results influence treatment decisions. The Southwest Oncology Group (SWOG) is conducting a large, prospective trial to address the clinical use of circulating tumor cells in breast cancer.
Medication Summary
Adjuvant treatment for breast cancer involves radiation therapy and a variety of chemotherapeutic and biologic agents. Adjuvant treatment of breast cancer is designed to treat micrometastatic disease, or breast cancer cells that have escaped the breast and regional lymph nodes but which have not yet had an established identifiable metastasis. Treatment is aimed at reducing the risk of future recurrence, thereby reducing breast cancer-related morbidity and mortality. The 2011 NCCN guidelines include recommendations for the use of two new drugs, denosumab and eribulin, both of which received FDA approval in 2010. The 2011 guidelines support the use of biologic denosumab for the prevention of skeletal events. When compared with zoledronic acid, denosumab, which is administered subcutaneously, delayed the onset of skeletal events by 8% and the time to multiple skeletal events by 23%. In addition, toxicities, such as hypercalcemia and renal failure, were less frequent. The guidelines recommend eribulin, an antimicrotubular drug, as the "preferred single agent" in chemotherapy treatment for women with advanced disease. Trials have shown significant improvement in survival when compared with patients receiving "treatment by physician's choice."[18] In June 2011, an FDA panel recommended that bevacizumab (Avastin) no longer be used to treat breast cancer, and in November officially rescinded its approval.
Antineoplastic Agents
Class Summary
Various chemotherapy regimens are recommended for the treatment of breast cancer. Common regimens include docetaxel, cyclophosphamide, doxorubicin, carboplatin, methotrexate, and trastuzumab, among others.
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Docetaxel (Taxotere)
Docetaxel is indicated for use in combination with doxorubicin and cyclophosphamide for adjuvant treatment of operable node-positive breast cancer. It is also indicated for locally advanced or metastatic breast cancer after failure of prior chemotherapy. It is a semisynthetic taxane, a class of drugs that inhibits cancer cell growth by promoting assembly and blocking the disassembly of microtubules, thereby preventing cancer cell division, leading to cell death.
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Carboplatin
Carboplatin is an analog of cisplatin. This is a heavy metal coordination complex that exerts its cytotoxic effect by platination of DNA, a mechanism analogous to alkylation, leading to interstrand and intrastrand DNA cross-links and inhibition of DNA replication. It binds to protein and other compounds containing the SH group. Cytotoxicity can occur at any stage of the cell cycle, but the cell is most vulnerable to the action of these drugs in the G1 and S phases. It has the same efficacy as cisplatin, but with a better toxicity profile. The main advantages over cisplatin include less nephrotoxicity and ototoxicity, not requiring extensive prehydration, and less likelihood of inducing nausea and vomiting; however, it is more likely to induce myelotoxicity.
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Doxorubicin (Liposomal)
Doxorubicin is a cytotoxic anthracycline that inhibits topoisomerase II and produces free radicals, which may cause destruction of DNA. It blocks DNA and RNA synthesis by inserting between adjacent base pairs and binding to the sugar-phosphate backbone of DNA, which causes DNA polymerase inhibition. It binds to nucleic acids, presumably by specific intercalation of the anthracycline nucleus with the DNA double helix. It is also a powerful iron chelator. The irondoxorubicin complex induces production of free radicals that can destroy DNA and cancer cells. Maximum toxicity occurs during the S phase of the cell cycle.
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Capecitabine (Xeloda)
Capecitabine is a pyrimidine analog, which, in combination with docetaxel, is indicated for metastatic breast cancer after the failure of prior anthracycline-containing chemotherapy. Monotherapy with capecitabine is indicated for the treatment of patients with metastatic breast cancer resistant to both paclitaxel and an anthracyclinecontaining chemotherapy regimen or resistant to paclitaxel and for whom further anthracycline therapy is not indicated.[12]
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Paclitaxel
Paclitaxel is indicated for adjuvant treatment of node-positive breast cancer (ie, administered sequentially to doxorubicin-containing combination chemotherapy). Dose-dense regimens (ie, more frequent administration) are currently being studied and resulting disease-free interval examined. Mechanisms of action are tubulin polymerization and microtubule stabilization, which, in turn, inhibit mitosis and may result in the breakage of chromosomes.
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Gemcitabine (Gemzar)
Gemcitabine is a pyrimidine analog that is metabolized intracellularly to an active nucleotide. It inhibits ribonucleotide reductase and competes with deoxycytidine triphosphate for incorporation into DNA. It is cell-cycle specific for the S phase. Gemcitabine, in combination with paclitaxel, is indicated as a first-line treatment for metastatic breast cancer after the failure of prior anthracycline-containing adjuvant chemotherapy (unless anthracyclines were clinically contraindicated).
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Cyclophosphamide
Cyclophosphamide is chemically related to nitrogen mustards. It is indicated for use in patients with carcinoma of the breast. It is activated in the liver to its active metabolite, 4hydroxycyclophosphamide, which alkylates the target sites in susceptible cells in an all-or-none type of reaction. As an alkylating agent, the mechanism of action of the active metabolites may involve cross-linking of DNA, which may interfere with the growth of normal and neoplastic cells.
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Methotrexate (Trexall)
Methotrexate is an antimetabolite that inhibits dihydrofolate reductase, thereby hindering DNA synthesis and cell reproduction in malignant cells. Methotrexate is indicated alone or in combination with other anticancer agents for the treatment of breast cancer.
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Epirubicin (Ellence)
Epirubicin is indicated as a part of adjuvant therapy in patients with evidence of axillary-node tumor involvement following resection of primary breast cancer.[13] It is a cell cycle phase inhibitor nonspecific anthracycline derivative of doxorubicin with maximum cytotoxic effects on the S and G2 phases of the cell cycle.
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Vinorelbine (Navelbine)
Vinorelbine is a semisynthetic vinca alkaloid that inhibits tubulin polymerization during the G2 phase of cell division, thereby inhibiting mitosis.
The indication for metastatic breast cancer (HER2-negative) was revoked by the FDA in November 2011 due to failure to delay tumor growth or provide survival benefit. The NCCN 2011 guidelines still recommend bevacizumab for targeted therapy[18] despite concerns expressed by the FDA.[19, 20]
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Trastuzumab (Herceptin)
Trastuzumab is a monoclonal antibody that binds to the extracellular human epidermal growth receptor 2 (HER2). It mediates antibody-dependent cellular cytotoxicity against cells that overproduce HER2. It is indicated for adjuvant treatment of HER2-overexpressing, node-positive or node-negative (ER/PR negative or with one high-risk feature) breast cancer, as part of a treatment regimen consisting of doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel; with docetaxel and carboplatin; or as a single agent following multimodality anthracycline-based therapy. It is also used in combination with paclitaxel for first-line treatment of HER2-overexpressing metastatic breast cancer and as a single agent for treatment of HER2-overexpressing breast cancer in patients who have received one or more chemotherapy regimens for metastatic disease.[14]
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Pertuzumab (Perjeta)
Pertuzumab is an HER2/neu receptor antagonist that elicits action at a different ligand binding site from trastuzumab to prevent HER2 dimerization. It is indicated in combination with trastuzumab and docetaxel for treatment of HER2-positive metastatic breast cancer in patients who have not previously received anti-HER2 therapy or chemotherapy.
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Denosumab (Xgeva)
Monoclonal antibody that specifically targets RANK ligand, an essential regulator of osteoclasts. Indicated to prevent SREs (ie, bone fractures and pain) in patients with bone metastases from solid tumors.
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Bevacizumab (Avastin)
The indication for metastatic breast cancer (HER2-negative) was revoked by the FDA in November 2011 due to failure to delay tumor growth or provide survival benefit. bevacizumab is a murine derived monoclonal antibody that inhibits angiogenesis by targeting and inhibiting vascular endothelial growth factor (VEGF). Inhibiting new blood vessel formation denies blood, oxygen, and other nutrients needed for tumor growth. This agent is used in combination with standard chemotherapy.
Lapatinib (Tykerb)
Lapatinib is a 4-anilinoquinazoline kinase that inhibits intracellular tyrosine kinase domains of epidermal growth factor receptors (EGFR [ErbB1]) and HER2 (ErbB2). It is indicated in combination with capecitabine for advanced or metastatic breast cancer with tumors that over-express HER2 for which previous therapy (ie, anthracycline, taxane, and trastuzumab) was not effective. It is also used in combination with letrozole for the treatment of postmenopausal women with hormone receptor positive metastatic breast cancer tumors that over expresses the HER2 receptor for whom hormonal therapy is indicated.[15]
Aromatase Inhibitors
Class Summary
Aromatase inhibitors play a role in adjuvant therapy in breast cancer. These agents work by inhibiting aromatase, the enzyme responsible for converting other steroid hormones into estrogen.
Anastrozole (Arimidex)
Anastrozole significantly lowers serum estradiol concentrations by inhibiting the conversion of adrenally generated androstenedione to estrone. It is used as first-line treatment of breast cancer in postmenopausal women with hormone receptorpositive or hormone receptorunknown locally advanced or metastatic disease. It is also used to treat advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy.
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Letrozole (Femara)
Letrozole is a nonsteroidal competitive inhibitor of the aromatase enzyme system. It inhibits the conversion of androgens to estrogens. Letrozole is indicated for the adjuvant treatment of postmenopausal women with hormone receptorpositive early breast cancer. It is also used for firstline treatment of postmenopausal women with hormone receptorpositive or hormone receptor unknown locally advanced or metastatic breast cancer. It is also indicated for the treatment of advanced breast cancer in postmenopausal women with disease progression following antiestrogen therapy and for the extended adjuvant treatment of early breast cancer in postmenopausal women who have received 5 years of adjuvant tamoxifen therapy.[16]
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Exemestane (Aromasin)
Exemestane elicits irreversible steroidal aromatase inactivation by acting as a false substrate for the aromatase enzyme. It binds irreversibly to the aromatase enzyme active site, causing inactivation (ie, suicide inhibition). It significantly lowers circulating estrogen concentrations in postmenopausal women. It differs from tamoxifen in that it inhibits estrogen production, whereas tamoxifen inhibits estrogen at the receptor site. It is indicated for advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy.
Bisphosphonate Agents
Class Summary
Bisphosphonates are complementary to chemotherapy and hormone therapy because they may lessen the damage to bone from metastatic disease. Bisphosphonates inhibit osteoclast function and reduce the resorption of bone.
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Tamoxifen
SERMs stimulate or inhibit the estrogen receptors of various target tissues. Examples of SERMs include tamoxifen, raloxifene, and toremifene.
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Raloxifene (Evista)
Raloxifene is a selective nonsteroidal benzothiophene, estrogen receptor modulator. It is indicated for risk reduction for invasive breast cancer in postmenopausal women with osteoporosis. In addition, it is indicated for risk reduction in invasive breast cancer in postmenopausal women at high risk of invasive breast cancer.
Toremifene (Fareston)
Toremifene is a nonsteroidal triphenylethylene derivative that binds to estrogen receptors. It may exert estrogenic activities, antiestrogenic activities, or both activities. It is indicated for metastatic breast cancer in postmenopausal women with estrogen-receptorpositive or unknown tumors.[17]
Antimicrotubular agent
Class Summary
May consider use in patients who have received at least 2 chemotherapeutic regimens for metastatic disease.
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Eribulin (Halaven)
Microtubule inhibitor. Inhibits growth phase of microtubules, leading to G2/M cell-cycle block, disruption of mitotic spindles, and, ultimately, apoptotic cell death. Indicated for metastatic breast cancer in patients who have previously received at least 2 chemotherapeutic regimens for the treatment of metastatic disease. Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting.