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Dr Sriram
Dr Dinesh
Dr Pareekshith
Department of GENERAL SURGERY
MMCH AND RESEARCH
CENTER,CALICUT
MENTOR: Dr. C. M. Lakshminarayanan
Professor & HOD
 Incidence
 Risk factors
 Etiopathogenesis
 Clinical features
 Management
 Recent advancements
 Breast cancer is SECOND most common cancers
affecting females.
 It is the 2nd most common cause of death due to
cancer in women after Lung cancer.
 one in 100 Indian females is likely to develop breast
cancer during her lifetime.
Age
Gender
Race
Country of birth
Family History
Genetic Risks
Personal History
Certain types of
benign breast
disesase
Menstrual History
Reproductive History
Oral Contraceptives
Hormone Replacement
Alcohol
Diet
Obesity
Ionising radiation
Nonmodifiable Risks Modifiable Risks
 Age
Increases with age.
Mostly common in middle age group
Gender
average risk for women in life time-12.2%
More common in women than men (150:1)

Country of birth
More common in West
Sporadic breast cancer 65-75%
Familial breast cancer 20-30%
Hereditary breast cancer 5-10%
Family History
 1st degree relatives of patient-> risk increased by
2 or 3 fold
Risk is much higher if
-B/L carcinoma
-Early onset 50% risk
-Multiple members
Family history of ovarian cancer
BRCA 1 BRCA 2
Long arm of chromosome 17 Long arm of chromosome 13
40% of familial breast CA 20-30% familial breast CA
45% of lifetime risk for ovarian CA. 30% of ovarian CA
High grade Low grade
Hormone receptor negative Positive
Unfavourable prognosis. Favourable prognosis.
Genetic factors
 SYNDROMES ASSOCIATED WITH
BREAST CANCER:
SYNDROME GENE MUTATION
- Li-Fraumeni syndrome P53
- Cowden’s syndrome PTEN
- Muir syndrome MSH2 / MLH1
- Ataxia telengiectasia ATM
-Putz-jeghrs syndrome STK11/LKB1
Personal History of Previous Cancer
 3- to 4-fold increased risk
 Contralateral breast
 Ovary
 Endometrium
 Certain Types of Benign breast diseases
Type Relative risk
Non proliferative disease 1
Proliferative without atypia 1.3-1.9
Proliferative with atypia 3.7-4.2
Ductal involvement by cells of atypical ductal
hyperplasia
>7
 Menarche < age 12 increases risk
 Menopause > age 55 increases risk
 1st child after age 30 or nulliparous
 Prolonged combined estrogen & progesterone
replacement therapy
 OCP’S- ???
 BILATERAL OOPHORECTOMY BEFORE THE AGE OF 40
YEARS IS PROTECTIVE AGAINST BREAST CANCER.
 Diet
 Alcohol
 High fat diet
 Irradiation
 Risk factors for young women
 Hodgkin lymphoma and fluoroscopic tests
 Obesity
 Androstenodione Estrone
 Radial scar
Adipose tissue
 BREAST FEEDING IS PROTECTIVE
 SMOKING AND OCP ARE NOT PROVED TO BE
RISK FACTOR FOR CARCINOMA BREAST
GAIL MODEL
Computer model available that can calculate an
individual woman’s 5-yr risk of breast cancer
Developed by the National Cancer Institute
Utilizes a series of questions to calculate risk based on
nonmodifiable & modifiable factors
Administered by a health care professional
 Histopathology
Cancer cells are
divided
Invading
through
basement
membrane
Invasive
carcinoma
No
Carcinoma in
situ
Classification of
breast cancer
In situ
(15-30%)
Ductal
carcinima
insitu (80%)
Lobular
carcinoma
insitu
(20%)
Invasive
(70-85%)
Invasive ductal
carcinoma
with
productive
fibrosis (80%)
Invasive
lobular
carcinoma
(10%)
Mucinous
(colloid)
(2.4%)
Tubular
(1.5%) Medullary
(1.2%)
Papillary
(1%)
Subtype ER Her- 2 -Neu Ki67
Luminal A +ve -ve Low
Luminal B +ve +ve High
Her-2-Neu over
expression group
-ve +ve High
Basal cell like ER and PR -ve -ve High
Claudin-Low -ve -ve High
 HISTORY AND PHYSICAL EXAMINATION
 RADIOLOGICAL ASSESSMENT
 PATHOLOGICAL ASSESSMENT
 MAMMOGRAPHY
 ULTRASONOGRAPHY
 MAGNETIC RESONANCE IMAGING
 To distinguish scar from recurrence in women
who have had previous breast conservation
therapy for cancer
 To assess multifocality and multicentricity in
lobular cancer and to assess the extent of
high-grade ductal carcinoma in situ (DCIS). It
is less useful in low-grade DCIS;
 It is the best imaging modality for the
breasts of women with implants;
 As A screening tool in high-risk women
(because of family history
 FINE NEEDLE ASPIRATION BIOPSY
 CORE NEEDLE BIOPSY
 EXCISIONAL BIOPSY
 LFT
 USG abdomen and pelvis.
 Biopsy of metastatic lesion – very important (
biomarkers may differ in primary and
secondary deposits)
 Pleural fluid analysis, Ascitic fluid analysis.
 CT CHEST & ABDOMEN.
 MRI/ PET CT
 Whole body scan.
 CHEST XRAY
 „ECG
 „Blood for hemoglobin, total leukocyte count
(TLC), differential leukocyte count (DLC)
and
 Erythrocyte sedimentation rate (ESR)
 „Blood for sugar, urea and creatinine.
 Blood grouping and typing
 1. BCS + SLN biopsy +RT
 2. MRM
WITH ADJUVANT
SYSTEMIC
THERAPY
• NEAOADJUVANT CHEMOTHERAPY
• BCS/MRM
• RADIOTHERAPY
Primary goal of therapy
 Improvement and maintenance of Quality of life
 Prolongation of survival
 Main stay of treatment is AGGRESSIVE
CHEMOTHERAPY
 More useful in hormone negative tumours.
 Hormone positive tumours not responding to
ET
 Patients with symptomatic visceral
metastasis.
 BONE METASTASIS
 Rx – Bisphosphonates IV (Zolendronic acid-
4mg,Pamidronate-90mg) RT
 Internal fixation, spinal decompression,
laminectomy.
 ORAL Calcium and Vitamin D3
supplements
 Brain mets
Localised Surgery
Steroid followed by RT
 Spine
Steroid with decompression and
stabilization
 Malignant Ascites
Symptomatic > diuretics,
Paracentesis
Peritoneo venous shunts
 Limited role
 Radiotherapy
BIOMARKERS
RECEPTORS
PATHOLOGY
IMAGING MODALITIES
CLASSIFICATIONS
SURGICAL APPROACH
CHEMOTHERAPY
 BC1, BC2, BC3
 BC3 posses highest individual diagnostic
power
 CA15-3, CA27-79, KK-LC-1,
 KK-LC-1[kita-Kyushu lung antigen-1]
expressed in triple negative breast
cancer
 IGF-1, E-Cadherin , PTEN
 Loss of E Cadherin is hallmark of invasive
lobular carcinoma
 LIQUID BIOPSY
 RADIOACTIVE SEED LOCALIZATION- I125
 STEREOTACTIC MAMMOGRAPHIC CORE
NEEDLE BIOPSY
 NEEDLE LOCALIZED BIOPSY UNDER
MAMMOGRAPHY
 VACUUM ASSISTED BIOPSY
 MRI GUIDED CORE NEEDLE BIOPSY
 Xero mammography- dense breasts
 PET/CT
 PET/MRI
 Breast ductal endoscopy
 Diffusion Weighted Imaging with ADC
 Thermography
 MRI is superior to mammography in
detecting cancer in patients receiving HRT
and young females
 One view breast tomosynthesis- least
radiation dose
 Based on genomic hybridization
 Cluster A- poor prognosis
 Cluster B- good prognosis
 ILC BASED ON RECEPTOR STATUS
 Skin sparing mastectomy/ key hole
mastectomy
 Nipple sparing mastectomy
 Oncoplasty
 NEWLY APPROVED DRUGS
 Ixabepilone - Anthracycline and taxane
resistant cases
 Lapatinib - Second line HER2new therapy
 Sunitinib - Refractory metastatic breast
cancers
 Bevacizumab – monoclonal antibody against
VEGF
 Nelipepimut-S :- Investigating as vaccine
to prevent clinical recurrence in high risk
patients
 Pembrolizumab- monoclonal IgG4
antibody
 Fulvestrant – ER degrader
Breast carcinoma overview and recent advances in management
Breast carcinoma overview and recent advances in management

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Breast carcinoma overview and recent advances in management

  • 1.
  • 2. Dr Sriram Dr Dinesh Dr Pareekshith Department of GENERAL SURGERY MMCH AND RESEARCH CENTER,CALICUT MENTOR: Dr. C. M. Lakshminarayanan Professor & HOD
  • 3.  Incidence  Risk factors  Etiopathogenesis  Clinical features  Management  Recent advancements
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.  Breast cancer is SECOND most common cancers affecting females.  It is the 2nd most common cause of death due to cancer in women after Lung cancer.  one in 100 Indian females is likely to develop breast cancer during her lifetime.
  • 9.
  • 10. Age Gender Race Country of birth Family History Genetic Risks Personal History Certain types of benign breast disesase Menstrual History Reproductive History Oral Contraceptives Hormone Replacement Alcohol Diet Obesity Ionising radiation Nonmodifiable Risks Modifiable Risks
  • 11.  Age Increases with age. Mostly common in middle age group Gender average risk for women in life time-12.2% More common in women than men (150:1) 
  • 12. Country of birth More common in West Sporadic breast cancer 65-75% Familial breast cancer 20-30% Hereditary breast cancer 5-10%
  • 13. Family History  1st degree relatives of patient-> risk increased by 2 or 3 fold Risk is much higher if -B/L carcinoma -Early onset 50% risk -Multiple members Family history of ovarian cancer
  • 14. BRCA 1 BRCA 2 Long arm of chromosome 17 Long arm of chromosome 13 40% of familial breast CA 20-30% familial breast CA 45% of lifetime risk for ovarian CA. 30% of ovarian CA High grade Low grade Hormone receptor negative Positive Unfavourable prognosis. Favourable prognosis. Genetic factors
  • 15.  SYNDROMES ASSOCIATED WITH BREAST CANCER: SYNDROME GENE MUTATION - Li-Fraumeni syndrome P53 - Cowden’s syndrome PTEN - Muir syndrome MSH2 / MLH1 - Ataxia telengiectasia ATM -Putz-jeghrs syndrome STK11/LKB1
  • 16. Personal History of Previous Cancer  3- to 4-fold increased risk  Contralateral breast  Ovary  Endometrium  Certain Types of Benign breast diseases Type Relative risk Non proliferative disease 1 Proliferative without atypia 1.3-1.9 Proliferative with atypia 3.7-4.2 Ductal involvement by cells of atypical ductal hyperplasia >7
  • 17.  Menarche < age 12 increases risk  Menopause > age 55 increases risk  1st child after age 30 or nulliparous  Prolonged combined estrogen & progesterone replacement therapy  OCP’S- ???  BILATERAL OOPHORECTOMY BEFORE THE AGE OF 40 YEARS IS PROTECTIVE AGAINST BREAST CANCER.
  • 18.
  • 19.  Diet  Alcohol  High fat diet  Irradiation  Risk factors for young women  Hodgkin lymphoma and fluoroscopic tests  Obesity  Androstenodione Estrone  Radial scar Adipose tissue
  • 20.  BREAST FEEDING IS PROTECTIVE  SMOKING AND OCP ARE NOT PROVED TO BE RISK FACTOR FOR CARCINOMA BREAST
  • 21. GAIL MODEL Computer model available that can calculate an individual woman’s 5-yr risk of breast cancer Developed by the National Cancer Institute Utilizes a series of questions to calculate risk based on nonmodifiable & modifiable factors Administered by a health care professional
  • 22.
  • 23.
  • 24.  Histopathology Cancer cells are divided Invading through basement membrane Invasive carcinoma No Carcinoma in situ
  • 25. Classification of breast cancer In situ (15-30%) Ductal carcinima insitu (80%) Lobular carcinoma insitu (20%) Invasive (70-85%) Invasive ductal carcinoma with productive fibrosis (80%) Invasive lobular carcinoma (10%) Mucinous (colloid) (2.4%) Tubular (1.5%) Medullary (1.2%) Papillary (1%)
  • 26.
  • 27. Subtype ER Her- 2 -Neu Ki67 Luminal A +ve -ve Low Luminal B +ve +ve High Her-2-Neu over expression group -ve +ve High Basal cell like ER and PR -ve -ve High Claudin-Low -ve -ve High
  • 28.
  • 29.
  • 30.
  • 31.  HISTORY AND PHYSICAL EXAMINATION  RADIOLOGICAL ASSESSMENT  PATHOLOGICAL ASSESSMENT
  • 32.  MAMMOGRAPHY  ULTRASONOGRAPHY  MAGNETIC RESONANCE IMAGING
  • 33.
  • 34.  To distinguish scar from recurrence in women who have had previous breast conservation therapy for cancer  To assess multifocality and multicentricity in lobular cancer and to assess the extent of high-grade ductal carcinoma in situ (DCIS). It is less useful in low-grade DCIS;  It is the best imaging modality for the breasts of women with implants;  As A screening tool in high-risk women (because of family history
  • 35.  FINE NEEDLE ASPIRATION BIOPSY  CORE NEEDLE BIOPSY  EXCISIONAL BIOPSY
  • 36.  LFT  USG abdomen and pelvis.  Biopsy of metastatic lesion – very important ( biomarkers may differ in primary and secondary deposits)  Pleural fluid analysis, Ascitic fluid analysis.  CT CHEST & ABDOMEN.  MRI/ PET CT  Whole body scan.
  • 37.
  • 38.
  • 39.
  • 40.  CHEST XRAY  „ECG  „Blood for hemoglobin, total leukocyte count (TLC), differential leukocyte count (DLC) and  Erythrocyte sedimentation rate (ESR)  „Blood for sugar, urea and creatinine.  Blood grouping and typing
  • 41.
  • 42.
  • 43.  1. BCS + SLN biopsy +RT  2. MRM WITH ADJUVANT SYSTEMIC THERAPY
  • 44. • NEAOADJUVANT CHEMOTHERAPY • BCS/MRM • RADIOTHERAPY
  • 45. Primary goal of therapy  Improvement and maintenance of Quality of life  Prolongation of survival
  • 46.  Main stay of treatment is AGGRESSIVE CHEMOTHERAPY  More useful in hormone negative tumours.  Hormone positive tumours not responding to ET  Patients with symptomatic visceral metastasis.
  • 47.  BONE METASTASIS  Rx – Bisphosphonates IV (Zolendronic acid- 4mg,Pamidronate-90mg) RT  Internal fixation, spinal decompression, laminectomy.  ORAL Calcium and Vitamin D3 supplements
  • 48.  Brain mets Localised Surgery Steroid followed by RT  Spine Steroid with decompression and stabilization  Malignant Ascites Symptomatic > diuretics, Paracentesis Peritoneo venous shunts
  • 49.  Limited role  Radiotherapy
  • 50.
  • 51.
  • 53.  BC1, BC2, BC3  BC3 posses highest individual diagnostic power  CA15-3, CA27-79, KK-LC-1,  KK-LC-1[kita-Kyushu lung antigen-1] expressed in triple negative breast cancer
  • 54.  IGF-1, E-Cadherin , PTEN  Loss of E Cadherin is hallmark of invasive lobular carcinoma
  • 55.  LIQUID BIOPSY  RADIOACTIVE SEED LOCALIZATION- I125  STEREOTACTIC MAMMOGRAPHIC CORE NEEDLE BIOPSY  NEEDLE LOCALIZED BIOPSY UNDER MAMMOGRAPHY  VACUUM ASSISTED BIOPSY  MRI GUIDED CORE NEEDLE BIOPSY
  • 56.  Xero mammography- dense breasts  PET/CT  PET/MRI  Breast ductal endoscopy  Diffusion Weighted Imaging with ADC  Thermography
  • 57.  MRI is superior to mammography in detecting cancer in patients receiving HRT and young females  One view breast tomosynthesis- least radiation dose
  • 58.  Based on genomic hybridization  Cluster A- poor prognosis  Cluster B- good prognosis
  • 59.  ILC BASED ON RECEPTOR STATUS
  • 60.
  • 61.  Skin sparing mastectomy/ key hole mastectomy  Nipple sparing mastectomy  Oncoplasty
  • 62.
  • 63.  NEWLY APPROVED DRUGS  Ixabepilone - Anthracycline and taxane resistant cases  Lapatinib - Second line HER2new therapy  Sunitinib - Refractory metastatic breast cancers  Bevacizumab – monoclonal antibody against VEGF
  • 64.  Nelipepimut-S :- Investigating as vaccine to prevent clinical recurrence in high risk patients  Pembrolizumab- monoclonal IgG4 antibody  Fulvestrant – ER degrader