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Speaker:
Shubham Kumar Gupta
Student, 3rd Prof. MBBS (Part-II)
BIG PICTURE…
 LYMPHATIC DRAINAGE OF BREAST
 EPIDEMIOLOGY & RISK FACTORS
 SCREENING MODALITIES
 BREAST BIOPSY TECHNIQUES
 TNM STAGING
 EARLY BREAST CANCER
 LOCALLY ADVANCED BREAST CANCER
 HORMONAL STATUS
 AXILLARY LYMPH NODE DISSECTION
 BREAST CA METASTASIS
 CA BREAST DURING PREGNANCY
 PAGET’S DISEASE OF BREAST
 INFLAMMATORY BREAST CA
AXILLARY GROUPS OF LYMPH NODES
LEVEL RELATION TO PECTORALIS MINOR INCLUDES
I LATERAL ANTERIOR,
POSTERIOR,
LATERAL
II SUPERFICIAL / DEEP CENTRAL LNs,
ROTTER’S LN*
III MEDIAL APICAL
* Although AJCC considers them to be axillary LNs, they are not so from an
anatomical point of view.
Lymphatic Drainage of
Breast
Epidemiology
EPIDEMIOLOGY - Worldwide :
• Most common cancer in women
• Leading cause of death from cancer for women aged 20-59 yrs.
• 29% of all newly diagnosed cancers in females
• 14% of the cancer-related deaths in women.
EPIDEMIOLOGY - India (2012) :
• Accounts 27% of all malignant cases.
• Incidence rate 25.8 per lakh population
• For every 2 women newly diagnosed with breast cancer,
one lady is dying of it. [144937 / 70218 = 2.06 = round it off to 2]
RISK FACTORS FOR BREAST CA
• Non-Modifiable:
Geographical factors
Age
Menstrual factors
Genetic predisposition
Family history
History of irradiation
• Modifiable:
Reproductive factors
Obesity
Alcohol
HRT
Decreased physical activity
RISK FACTORS FOR BREAST CA
RISK FACTORS FOR BREAST CA
• Histological risk factors:
 Proliferative Breast disease
 Atypical ductal Hyperplasia
 Atypical lobular hyperplasia
 Lobular Carcinoma-insitu (LCIS)
Risk Assessment Model
(Gail)
• Developed from case-control data in the Breast Cancer
Detection Demonstration Project; aka the Gail model).
• Incorporates age, age at menarche, age at first live birth,
the number of breast biopsy specimens, any history of
atypical hyperplasia, and number of first-degree relatives
with breast cancer.
• Predicts the cumulative risk of breast cancer according to
decade of life.
• Underestimate the risk for a BRCA1 or BRCA2 mutation
carrier.
• Not used in women with a diagnosis of LCIS or DCIS.
CLASSIFICATION OF BREAST CANCER
NON-INVASIVE EPITHELIAL CANCERS
• LCIS
• DCIS/INTRA-DUCTAL CA – Papillary, Cribriform, Solid, Comedo
INVASIVE EPITHELIAL CANCERS (% OF TOTAL)
• Invasive Lobular Ca (10%)
• Invasive Ductal Ca
Tubular Ca (2%)
Mucinous Ca (2%)
Medullary Ca(5%)
Invasive Cribriform Ca (1-2%)
Invasive Papillary Ca (1-2%)
Adenoid Cystic Ca (1%)
Metaplastic Ca (1%)
Invasive ductal Ca, NOS (50-70%)
MIXED TUMORS
• Carcinosarcoma
• Angiosarcoma
• Adenocarcinoma
SCREENING MODALITIES
 Self-examination of breast
 Clinical breast evaluation
 Mammography
 Ultrasonography
 Breast MRI (newest recomd.)
# Lifetime Risk Assessment
Breast Self-Examination
(BSE)
What to look for?
 Irregular changes in the size and shape of breast
 Lump in the breast
 Irregularity in nipple discharge or tenderness
 Awkward changes in the skin of the breast
Benefits:
 Early detection remains the primary defense available to patients in
preventing the development of life-threatening breast cancer
 For 50-74 year group  30% reduction in mortality
 For 40-49 year group  17% reduction in mortality
Clinical Breast Evaluation
(CBE)
• A complete bilateral breast examination should be
performed to look for :
– Variation in breast size
– Fungating masses
– Dimpling or retraction of the skin
– Nipple inversion or excoriation (classic finding of
Paget's disease of the breast, which also does not
present as a breast mass).
• Look for axillary lymph node enlargement.
MAMMOGRAPHY
Discussion of when to begin & how often to undergo screening
mammography has now become a more individualized discussion
with patients taking into account their breast cancer risk &
personal risk tolerance.
BI-RADS
BIRADS
Category
Description Likelihood
of
malignancy
Recommendation
0 Need more information 2-10% Further imaging needed
1 Normal 0.05-0.1% Routine screening mammography
2 Benign 0.05-0.1% Routine screening mammography
3 Probably benign 0.3-1.8% Short-term follow-up (6 months)
4 Highly suspicious 10-55% Biopsy
5 Malignant 60-100% Biopsy
6 Known Cancer 100% Treat malignancy
USG
 Assist in suspicious lesion detected on mammography or
physical examination
 Useful in the guidance of biopsies.
 Differentiating cystic from solid breast masses
 Breast cancer screening specifically in women with
dense breast tissue
 Limitations as screening test:
 Failure to detect microcalcifications
 Poor specificity (34%)
MRI
 Highly sensitive to detect malignant changes in the breast.
(independent of breast density )
 American Cancer Society MRI screening criteria :
 BRCA mutation
 First-degree relative with BRCA carrier but untested
 Lifetime risk approximately 20-25% or greater,
 Radiation to chest when aged 10-30 years
 Associated syndromes
 MRI has limited use as a screening tool:
 Cost. 10-fold higher cost than mammography
 Poor specificity (26%)  false-positive results
Risk Management
 Chemoprophylaxis :
 Tamoxifen
 Raloxifene.
 Prophylactic mastectomy :
 Reduce the chance of developing breast cancer by 90%.
 BRCA1 and BRCA2 mutation carriers treated with prophylactic
mastectomy
Breast Biopsy techniques
 FNAC / FNAB
 Core Needle Biopsy (CNB)
 Incisional Biopsy
 Excisional Biopsy
 Stereotactic core biopsy
 Vacuum-assisted biopsy
introduction, classification and prevention of breast cancer byShuvam

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introduction, classification and prevention of breast cancer byShuvam

  • 1. Speaker: Shubham Kumar Gupta Student, 3rd Prof. MBBS (Part-II)
  • 2. BIG PICTURE…  LYMPHATIC DRAINAGE OF BREAST  EPIDEMIOLOGY & RISK FACTORS  SCREENING MODALITIES  BREAST BIOPSY TECHNIQUES  TNM STAGING  EARLY BREAST CANCER  LOCALLY ADVANCED BREAST CANCER  HORMONAL STATUS  AXILLARY LYMPH NODE DISSECTION  BREAST CA METASTASIS  CA BREAST DURING PREGNANCY  PAGET’S DISEASE OF BREAST  INFLAMMATORY BREAST CA
  • 3. AXILLARY GROUPS OF LYMPH NODES
  • 4. LEVEL RELATION TO PECTORALIS MINOR INCLUDES I LATERAL ANTERIOR, POSTERIOR, LATERAL II SUPERFICIAL / DEEP CENTRAL LNs, ROTTER’S LN* III MEDIAL APICAL * Although AJCC considers them to be axillary LNs, they are not so from an anatomical point of view.
  • 6. Epidemiology EPIDEMIOLOGY - Worldwide : • Most common cancer in women • Leading cause of death from cancer for women aged 20-59 yrs. • 29% of all newly diagnosed cancers in females • 14% of the cancer-related deaths in women. EPIDEMIOLOGY - India (2012) : • Accounts 27% of all malignant cases. • Incidence rate 25.8 per lakh population • For every 2 women newly diagnosed with breast cancer, one lady is dying of it. [144937 / 70218 = 2.06 = round it off to 2]
  • 7. RISK FACTORS FOR BREAST CA • Non-Modifiable: Geographical factors Age Menstrual factors Genetic predisposition Family history History of irradiation
  • 9. RISK FACTORS FOR BREAST CA • Histological risk factors:  Proliferative Breast disease  Atypical ductal Hyperplasia  Atypical lobular hyperplasia  Lobular Carcinoma-insitu (LCIS)
  • 10. Risk Assessment Model (Gail) • Developed from case-control data in the Breast Cancer Detection Demonstration Project; aka the Gail model). • Incorporates age, age at menarche, age at first live birth, the number of breast biopsy specimens, any history of atypical hyperplasia, and number of first-degree relatives with breast cancer. • Predicts the cumulative risk of breast cancer according to decade of life. • Underestimate the risk for a BRCA1 or BRCA2 mutation carrier. • Not used in women with a diagnosis of LCIS or DCIS.
  • 11. CLASSIFICATION OF BREAST CANCER NON-INVASIVE EPITHELIAL CANCERS • LCIS • DCIS/INTRA-DUCTAL CA – Papillary, Cribriform, Solid, Comedo INVASIVE EPITHELIAL CANCERS (% OF TOTAL) • Invasive Lobular Ca (10%) • Invasive Ductal Ca Tubular Ca (2%) Mucinous Ca (2%) Medullary Ca(5%) Invasive Cribriform Ca (1-2%) Invasive Papillary Ca (1-2%) Adenoid Cystic Ca (1%) Metaplastic Ca (1%) Invasive ductal Ca, NOS (50-70%) MIXED TUMORS • Carcinosarcoma • Angiosarcoma • Adenocarcinoma
  • 12. SCREENING MODALITIES  Self-examination of breast  Clinical breast evaluation  Mammography  Ultrasonography  Breast MRI (newest recomd.) # Lifetime Risk Assessment
  • 13. Breast Self-Examination (BSE) What to look for?  Irregular changes in the size and shape of breast  Lump in the breast  Irregularity in nipple discharge or tenderness  Awkward changes in the skin of the breast Benefits:  Early detection remains the primary defense available to patients in preventing the development of life-threatening breast cancer  For 50-74 year group  30% reduction in mortality  For 40-49 year group  17% reduction in mortality
  • 14. Clinical Breast Evaluation (CBE) • A complete bilateral breast examination should be performed to look for : – Variation in breast size – Fungating masses – Dimpling or retraction of the skin – Nipple inversion or excoriation (classic finding of Paget's disease of the breast, which also does not present as a breast mass). • Look for axillary lymph node enlargement.
  • 15. MAMMOGRAPHY Discussion of when to begin & how often to undergo screening mammography has now become a more individualized discussion with patients taking into account their breast cancer risk & personal risk tolerance.
  • 16. BI-RADS BIRADS Category Description Likelihood of malignancy Recommendation 0 Need more information 2-10% Further imaging needed 1 Normal 0.05-0.1% Routine screening mammography 2 Benign 0.05-0.1% Routine screening mammography 3 Probably benign 0.3-1.8% Short-term follow-up (6 months) 4 Highly suspicious 10-55% Biopsy 5 Malignant 60-100% Biopsy 6 Known Cancer 100% Treat malignancy
  • 17. USG  Assist in suspicious lesion detected on mammography or physical examination  Useful in the guidance of biopsies.  Differentiating cystic from solid breast masses  Breast cancer screening specifically in women with dense breast tissue  Limitations as screening test:  Failure to detect microcalcifications  Poor specificity (34%)
  • 18. MRI  Highly sensitive to detect malignant changes in the breast. (independent of breast density )  American Cancer Society MRI screening criteria :  BRCA mutation  First-degree relative with BRCA carrier but untested  Lifetime risk approximately 20-25% or greater,  Radiation to chest when aged 10-30 years  Associated syndromes  MRI has limited use as a screening tool:  Cost. 10-fold higher cost than mammography  Poor specificity (26%)  false-positive results
  • 19. Risk Management  Chemoprophylaxis :  Tamoxifen  Raloxifene.  Prophylactic mastectomy :  Reduce the chance of developing breast cancer by 90%.  BRCA1 and BRCA2 mutation carriers treated with prophylactic mastectomy
  • 20. Breast Biopsy techniques  FNAC / FNAB  Core Needle Biopsy (CNB)  Incisional Biopsy  Excisional Biopsy  Stereotactic core biopsy  Vacuum-assisted biopsy

Editor's Notes

  1. Breast cancer is the most common site-specific cancer in women and is the leading cause of death from cancer for women aged 20 to 59 years. It accounts for 29% of all newly diagnosed cancers in females and is responsible for 14% of the cancer-related deaths in women.
  2. The boundaries for lymph drainage of the axilla are not well demarcated, and there is considerable variation in the position of the axillary lymph nodes. The 5 axillary lymph node groups are: The lateral grp lie medial or posterior to the axillary vein. The external mammary group (anterior or pectoral group) - lie along the lower border of the pectoralis min or muscle contiguous with the lateral thoracic vessels and receive most of the lymph drainage from the lateral aspect of the breast. The scapular group (posterior or subscapular) - lie along the posterior wall of the axilla at the lateral border of the scapula contiguous with the subscapular vessels. The central group - embedded in the fat of the axilla lying immediately posterior to the pectoralis minor muscle and receive lymph drainage both from the axillary vein, external mammary, and scapular groups of lymph nodes and directly from the breast; The subclavicular group (apical) - lie posterior and superior to the upper border of the pectoralis minor muscle and receive lymph drainage from all of the other groups of axillary lymph nodes. And The interpectoral group (Rotter's) are interposed between the pectoralis major and pectoralis minor muscles and receive lymph drainage directly from the breast. The lymph fluid that passes through the interpectoral group of lymph nodes passes directly into the central and subclavicular groups.
  3. Axillary lymph nodes Axillary lymph nodes are classified according to their anatomic location relative to the pectoralis minor muscle. Level I nodes. Lateral to the pectoralis minor muscle Level II nodes. Posterior to the pectoralis minor muscle Level III nodes. Medial to the pectoralis minor muscle and most accessible with division of the muscle Rotter's nodes. Between the pectoralis major and the minor muscles
  4. The lymphatics draining the breast are divided into two groups: (a) superficial and (b) deep. Superficial lymphatics drain - skin of the breast except that of nipple and areola. Deep lymphatics drain - parenchyma of the breast, and skin of the nipple and areola. A plexus of lymph vessels deep to the areola is called subareolar plexus of Sappey (Fig. 3.20). The subareolar plexus and most of the lymph from the breast drain into the anterior group of axillary lymph nodes. The superficial lymphatics of the breast of one side communicate with those of the opposite side. Consequently the unilateral malignancy may become bilateral. The lymphatic drainage from the breast occurs as follows (Fig. 3.21): 1. Lateral quadrants - anterior axillary or pectoral group. 2. Medial quadrants - internal mammary lymph nodes situated along the internal mammary artery. Some lymphatics may go to the internal mammary lymph nodes of the opposite side. 3. Few - lower lateral quadrant - posterior intercostal nodes [Follow the posterior intercostal arteries] 4. Few - lower medial quadrant - pierce the anterior abdominal wall and communicate with subdiaphragmatic and subperitoneal lymph plexuses. 5. The lymph vessels from the deep surface of the breast pierce pectoralis major and clavipectoral fascia to drain into the apical group of axillary lymph nodes (Fig. 3.22). N.B. About 75% of the lymph from the breast is drained into axillary nodes, 20% into internal mammary lymph nodes, and 5% into the posterior intercostal lymph nodes. Among the axillary lymph nodes, most of the lymph drains into the anterior axillary nodes and the remaining into posterior and apical groups. The lymph from anterior and posterior groups first goes to the central and lateral groups, and then through them into the supraclavicular lymph nodes.
  5. Breast cancer is the most common site-specific cancer in women and is the leading cause of death from cancer for women aged 20 to 59 years. It accounts for 29% of all newly diagnosed cancers in females and is responsible for 14% of the cancer-related deaths in women.
  6. Age : increasing (see your notes); Gender : Female Menstrual: Increased exposure to estrogen is associated with an increased risk for developing breast cancer, whereas reducing exposure is thought to be protective.42-48 Correspondingly, factors that increase the number of menstrual cycles, such as early menarche, nulliparity, and late menopause, are associated with increased risk. Early age @ menarche (<12yrs); Older age @ menopause (>55yrs); Genetic predisposition & Family history : see your notes H/o Irradiation : See your notes BRCA 1 – CHROMOSOME 17; GERMLINE MUTATION, AUTOSOMAL DOMINANT, BAD PROGNOSIS. BRCA 2 – CHROMOSOME 13; MORE CHANCE OF OVARIAN CANCER. MALE BREAST CANCER. In general, BRCA1-associated breast cancers are invasive ductal carcinomas, are poorly differentiated, are in the majority hormone receptor negative and have a triple receptor negative (immunohistochemical profile: ER-negative, PR-negative and HER-2-negative) or basal phenotype (based on gene expression profiling).
  7. Reproductive factors : Older age at first live birth, nulliparity, Lack of breast feeding. [The terminal differentiation of breast epithelium associated with a full-term pregnancy is also protective, so older age at first live birth is associated with an increased risk of breast cancer.] Obesity  increased breast cancer risk. Because the major source of estrogen in postmenopausal women is the conversion of androstenedione to estrone by adipose tissue, obesity is associated with a long-term increase in estrogen exposure. Alcohol consumption  increase serum levels of estradiol. Long-term consumption of foods with a high fat content contributes to an increased risk of breast cancer by increasing serum estrogen levels. Hormonal influence: Post-menopausal women on HRT with Estrogen + progestin combinations  High risk of developing Breast Ca. OCP: Do not increase the risk, not even in individuals at family history of Breast CA.
  8. To calculate breast cancer risk using the Gail model, a woman’s risk factors are translated into an overall risk score by multiplying her relative risks from several categories. This risk score is then compared with an adjusted population risk of breast cancer to determine the woman’s individual risk. This model is not appropriate for use in women with a known BRCA1 or BRCA2 mutation or women with lobular or ductal carcinoma in situ. Claus – more accurate if + family history; incorporates FH ovarian cancer. Unlike Gail does not include other risk factors; The Claus model provides individual estimates of breast cancer risk according to decade of life based on presence of first- and second-degree relatives with breast cancer and their age at diagnosis. Tyrer-Cusik (IBIS) – Risk of carrying BRCA 1/2 mutation and individual breast cancer risk – FH, other risk factors BRCAPRO – probability of having a BRCA 1/2 mutation with suggestive FH BrevaGEN – combines Gail + SNPs
  9. In high-risk women: say for those with known BRCA mutations, annual mammograms and semiannual physical examinations should begin at age 25 to 30 years. In patients with a strong family history of breast cancer but undocumented genetic mutation, annual mammograms and semiannual physical examinations should begin 10 years earlier than the age of the youngest affected relative and no later than age 40 years.
  10. 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. The American Cancer Society and the American College of Radiology still recommend annual screening starting at age 40, although we know that mammography is less sensitive in younger women due to breast density. It is also unclear if mammograms need to be performed every year. The discussion of when to begin and how often to undergo screening mammography has now become a more individualized discussion with patients taking into account their breast cancer risk, personal risk tolerance, and overall values. Currently it is the best available population-based method to detect breast cancer at an early stage, when treatment is most effective Breast compression to flatten the breast maximum amount of tissue can be imaged and examined. allows for a lower X-ray dose immobilization of the breast to reduce motion blur. reduces X-ray scatter, which may degrade the image. may cause some discomfort,
  11. Regarding the interpretation of mammography. The American College of Radiology (ACR) has established the Breast Imaging Reporting and Data System (BI-RADS) to guide the breast cancer diagnostic routine. For referring physicians, the BI-RADS categories indicate the patient’s risk of malignancy and recommend a specific course of action. Of all of the screening mammograms performed annually, approximately 90% show no evidence of cancer. On necessary further diagnostic testing, approximately 2% of all screening mammograms are shown to be abnormal and require biopsy. Among cases referred for biopsy, approximately 80% of the abnormalities are shown to be benign, and 20% are shown to be cancerous. The current recommendation from the National Cancer Institute and American College of Surgeons is annual screening mammography for women aged 40 years and older. Breast lesions on mammograms are classified according to the American College of Radiology by BI-RADS (Breast Imaging Reporting and Database System) scores:
  12. Ultrasonography can effectively distinguish solid masses from cysts, which account for approximately 25 percent of breast lesions. It is more sensitive than mammography in detecting lesions in women with dense breast tissue. It is useful in discriminating between benign and malignant solid masses. malignancy USG will show: Internal echoes Solid mass Irregular border
  13. MRI imaging of the breast revealing multifocal tumors not detected with standard breast imaging
  14. Several important medical decisions may be affected by a woman’s underlying risk of developing breast cancer. These decisions include when to use postmenopausal hormone replacement therapy, at what age to begin mammography screening or incorporate magnetic resonance imaging (MRI) screening, when to use tamoxifen to prevent breast cancer, and when to perform prophylactic mastectomy to prevent breast cancer Tamoxifen is an estrogen antagonist with proven benefit for the treatment of estrogen receptor (ER)–positive breast cancer. Raloxifene is a selective ER modulator(SERM). For women with an estimated lifetime risk of 40%, prophylactic mastectomy added almost 3 years of life, whereas for women with an estimated lifetime risk of 85%, prophylactic mastectomy added >5 years of life. Tamoxifen therapy currently is recommended only for women who have a Gail relative risk of 1.66% or higher, who are aged 35 to 59, women over the age of 60 or women with a diagnosis of LCIS or atypical ductal or lobular hyperplasia. S/E : deep vein thrombosis occurs 1.6 times as often, pulmonary emboli 3.0 times as often, and endometrial cancer 2.5 times as often in women taking tamoxifen. Cataract surgery is required almost twice as often among women taking tamoxifen.
  15. See printed notes Fine needle aspiration Biopsy (FNAB): Simplicity, readily available, relatively atraumatic for the patient. Limitation of the FNAB is availability of a experienced cytopathologist for interpretation of the results. Major limitation of FNAB is the inability of the cytology to distinguish invasive cancer from in situ disease. Core Needle Biopsy (CNB): automated gun attached to 14 / 18 gauge cutting needle. Tissue cores can be processed for complete pathologic assessment HP & Immuno-histochemistry. Sensitivity rate for CNB are almost 100% for diagnosing the breast lesions. FNAC / core biopsy:  In a clinically and mammographically suspicious mass, sensitivity and specificity of FNAC approaches 100%.  FNAC requires an experienced cytopathologist for accurate interpretation Histopathologic type and grade of malignancy, ER / PR receptor status, HER2/neu status can also be reported on cytopathology by an experienced cytopathologist using a cell block.  False negative rate for core needle biopsy is very low. However, a tissue specimen that does not show breast cancer cannot conclusively rule out malignancy as sampling error can occur.  Histologic type and grade of malignancy, receptor status and HER2/neu status can be easily made out on core needle biopsy.  Any patient scheduled for neoadjuvant chemotherapy should have the tumour pathology type and grade, receptor and HER2/neu status documented either on FNAC or core needle biopsy before starting chemotherapy, for in patients with complete response to chemotherapy, there will be no tumour tissue in the surgical specimen. Incisional Biopsy: done in a fungating breast mass. The edge biopsy with some normal skin margin is taken in fungating breast mass.  Some cases of inflammatory breast cancer may also be suitable for incisional biopsy if core biopsy is not diagnostic. Excisional biopsy: Any suspicious breast lesion in which histologic diagnosis was not possible by one of the needle biopsy techniques because of either technical considerations, then an excisional biopsy is indicated. Grossly, an attempt should be made to excise an approx. 1 cm thickness of normal appearing tissue surrounding the index lesion.