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Dr.K.Senthil Kumar
Oncology resident
 INTRODUCTION
 RISK FACTORS
 RISK ASSESMENT MODELS
 RISK REDUCTION INTERVENTIONS
 CARRY HOME
 lifetime risk of breast cancer in mutation
carriers
 47%–66% -BRCA1
 40%–57% BRCA2
 Family history 1.5 to 3 fold
 Personal history 0.5% to 1 % per year of
follow up
 Familial/genetic factors
 Demographic factors
 Reproductive history
 Lifestyle factor
 Irradiadition <30 yrs of age( 55 fold)
 breast density
 Factors number of breast biopsies
1. FEA
2. AH,LCIS
 BRCAPRO & BOADICEA
 GAIL MODEL
 CLAUSS MODEL
 TYRER-CUZICK MODEL
 screening with mammogram
 screening breast magnetic resonance
imaging
 clinical breast exams
 NON INVASIVE
1. LIFE STYLE
MODIFICATIONS
2. SURVEIILANCE
3. CHEMO
PREVENTION
 INVASIVE
1. RRM
2. RRSO
WHOM ? HOW?
 who do not want to
pursue RRS
 want to delay RRS,
 annual MRI in addition
to, and not instead
of, an annual
mammogram,
 30 YRS
SERM
AROMATASE INHIBITORS
BIGUANIDES
TAMOXIFEN (20 mg/d)
 pre- and postmenopausal patients ≥35 years
of age
 LE ≥10 years
 ≥1.7% 5-year risk for breast cancer as
determined by the modified Gail model
 LCIS (category 1)
 RALOXIFENE- 60 mg/Day
 STAR TRIAL ( NCCN)-tamoxifen -for most
postmenopausal patients desiring non-
surgical risk-reduction therapy - decrease
invasive cancer risk
 raloxifene 38% and tamoxifen 50%
 ASCO RECOMMENDATIONS
1. tamoxifen (in premenopausal women)
2. tamoxifen, raloxifene, or exemestane (in
postmenopausal women)
SERM
 Tamoxifen 20
mg/day
 Raloxifene 60
mg/day
AI’S
 25 mg/d of
exemestane
 1 mg/d of
anastrozole.
 [Not FDA
approved]
 50% Reduction incidence of cancer among
patients using METFORMIN for more than 4
years
 MECHANISM- directly and indirectly regulate
(through the insulin) the proliferation rate of
tumor progenitor cells in premalignant
lesions, preventing or delaying tumor
formation
 Endometrial cancer
 Cataract & Retinopathy
 BMD-Osteoporosis
 Thromboembolic Disease and Strokes
 EXERSISE & BMI
 ALCOHOL CONSUMPTION {<1 drink per day }
1 ounce of liquor,
6 ounces of wine
8 ounces of beer.
 Have a strong family history of breast cancer
 Have a personal history of breast cancer or
at present have breast cancer in one breast
 Have tested positive for BRCA1 or BRCA2
gene mutations
 Have been diagnosed with lobular carcinoma
in situ (LCIS)
 Have had radiation therapy to the chest
before age 30
 Have widely spread breast
microcalcifications or have dense breasts
 contralateral mastectomy synchronous with
the treatment of the primary tumor
 as a bilateral procedure in women at high
risk of developing this disease.
Bartlett in 1917
 Contralateral prophylactic mastectomy
 Bilsteral prophylactic mastectomy
 Prophylactic bilateral salphingo
oophorectomy
 SUBCUTANEOS MASTECTOMY
 SIMPLE MASTECTOMY
 SKIN SPARING MASTECTOMY –mc performed
mastectomy
 NIPPLE SPARING MASTECTOMY
 PROPHYLACTIC BILATERAL SALPHINGO
OOPHORECTOMY
 Rice and Strickler in 1951
 a rim of normal breast tissue was left
underneath the nipple-areolar complex (NAC)
 OBSOLETE – increased risk of recurrences
 Toth and Lambert -1991
 initial major concern was –residual breast
tissue remaining on the longer skin flaps,infra
mammary fold,axillary tail
 Barton et al disproved it – well planned incision-
to allow immeadiate reconstruction
 native skin allows for better appearance,
position, and shape of both prosthetic implants
&autologous reconstruction
 Strutures removed
1. Entire breast gland
2. NAC
3. Biopsy scar
4. Skin overlying the tumour
 Structures Preserved
1. Remaining skin
2. Infra mammary fold
 Type 1-only NAC removed
 Type 2-NAC +SKIN overlying the
tumour+BIOPSY site if any
 Type 3- similar to type 2 but resected
seperately leaving intact tissue in between
 Type 4 –NAC is removed along with certain
amount of skin
 Reduced post mastectomy deformity and
improved breast shape
 Scars are better and reduced
 Need for extensive tissue expansion and for
myo cutaneous flap is minimal
 Immaediate reconstruction has a beneficial
impact on patient’s psychology
 Freeman in 1962
 structures removed-Entire breast tissue
including the ductal tissue located in the
NAC
 Structures preserved -the entire skin( dermis
&epidermis) of the breast
 Bleeding
 Seroma
 Infectiom
 Flap necrosis
 Capsular contracture
 BRCA1/2 carriers- 53% reduction in risk of
breast cancer
Autologous flaps
 pedicled flap
 TRAM
 LD
Free flap
 DIEP flap
 SIEA flap
Prosthetics
 Silicon prosthesis
 Tissue expanders
 Several risk-reducing strategies exist
 identify high-risk patients
 High-risk surveillance with MRI as an adjunct
to mammography
 Chemoprevention
 Surgical prophylaxis remains the most
effective means to prevent breast cancer.
RISK REDUCTION STRATEGIES IN CA BREAST.pptx

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RISK REDUCTION STRATEGIES IN CA BREAST.pptx

  • 2.  INTRODUCTION  RISK FACTORS  RISK ASSESMENT MODELS  RISK REDUCTION INTERVENTIONS  CARRY HOME
  • 3.  lifetime risk of breast cancer in mutation carriers  47%–66% -BRCA1  40%–57% BRCA2  Family history 1.5 to 3 fold  Personal history 0.5% to 1 % per year of follow up
  • 4.  Familial/genetic factors  Demographic factors  Reproductive history  Lifestyle factor  Irradiadition <30 yrs of age( 55 fold)  breast density  Factors number of breast biopsies 1. FEA 2. AH,LCIS
  • 5.
  • 6.  BRCAPRO & BOADICEA  GAIL MODEL  CLAUSS MODEL  TYRER-CUZICK MODEL
  • 7.  screening with mammogram  screening breast magnetic resonance imaging  clinical breast exams
  • 8.  NON INVASIVE 1. LIFE STYLE MODIFICATIONS 2. SURVEIILANCE 3. CHEMO PREVENTION  INVASIVE 1. RRM 2. RRSO
  • 9. WHOM ? HOW?  who do not want to pursue RRS  want to delay RRS,  annual MRI in addition to, and not instead of, an annual mammogram,  30 YRS
  • 11. TAMOXIFEN (20 mg/d)  pre- and postmenopausal patients ≥35 years of age  LE ≥10 years  ≥1.7% 5-year risk for breast cancer as determined by the modified Gail model  LCIS (category 1)  RALOXIFENE- 60 mg/Day
  • 12.  STAR TRIAL ( NCCN)-tamoxifen -for most postmenopausal patients desiring non- surgical risk-reduction therapy - decrease invasive cancer risk  raloxifene 38% and tamoxifen 50%  ASCO RECOMMENDATIONS 1. tamoxifen (in premenopausal women) 2. tamoxifen, raloxifene, or exemestane (in postmenopausal women)
  • 13. SERM  Tamoxifen 20 mg/day  Raloxifene 60 mg/day AI’S  25 mg/d of exemestane  1 mg/d of anastrozole.  [Not FDA approved]
  • 14.
  • 15.  50% Reduction incidence of cancer among patients using METFORMIN for more than 4 years  MECHANISM- directly and indirectly regulate (through the insulin) the proliferation rate of tumor progenitor cells in premalignant lesions, preventing or delaying tumor formation
  • 16.  Endometrial cancer  Cataract & Retinopathy  BMD-Osteoporosis  Thromboembolic Disease and Strokes
  • 17.  EXERSISE & BMI  ALCOHOL CONSUMPTION {<1 drink per day } 1 ounce of liquor, 6 ounces of wine 8 ounces of beer.
  • 18.  Have a strong family history of breast cancer  Have a personal history of breast cancer or at present have breast cancer in one breast  Have tested positive for BRCA1 or BRCA2 gene mutations  Have been diagnosed with lobular carcinoma in situ (LCIS)  Have had radiation therapy to the chest before age 30  Have widely spread breast microcalcifications or have dense breasts
  • 19.
  • 20.  contralateral mastectomy synchronous with the treatment of the primary tumor  as a bilateral procedure in women at high risk of developing this disease.
  • 21. Bartlett in 1917  Contralateral prophylactic mastectomy  Bilsteral prophylactic mastectomy  Prophylactic bilateral salphingo oophorectomy
  • 22.  SUBCUTANEOS MASTECTOMY  SIMPLE MASTECTOMY  SKIN SPARING MASTECTOMY –mc performed mastectomy  NIPPLE SPARING MASTECTOMY  PROPHYLACTIC BILATERAL SALPHINGO OOPHORECTOMY
  • 23.  Rice and Strickler in 1951  a rim of normal breast tissue was left underneath the nipple-areolar complex (NAC)  OBSOLETE – increased risk of recurrences
  • 24.  Toth and Lambert -1991  initial major concern was –residual breast tissue remaining on the longer skin flaps,infra mammary fold,axillary tail  Barton et al disproved it – well planned incision- to allow immeadiate reconstruction  native skin allows for better appearance, position, and shape of both prosthetic implants &autologous reconstruction
  • 25.  Strutures removed 1. Entire breast gland 2. NAC 3. Biopsy scar 4. Skin overlying the tumour  Structures Preserved 1. Remaining skin 2. Infra mammary fold
  • 26.  Type 1-only NAC removed  Type 2-NAC +SKIN overlying the tumour+BIOPSY site if any  Type 3- similar to type 2 but resected seperately leaving intact tissue in between  Type 4 –NAC is removed along with certain amount of skin
  • 27.
  • 28.  Reduced post mastectomy deformity and improved breast shape  Scars are better and reduced  Need for extensive tissue expansion and for myo cutaneous flap is minimal  Immaediate reconstruction has a beneficial impact on patient’s psychology
  • 29.  Freeman in 1962  structures removed-Entire breast tissue including the ductal tissue located in the NAC  Structures preserved -the entire skin( dermis &epidermis) of the breast
  • 30.
  • 31.  Bleeding  Seroma  Infectiom  Flap necrosis  Capsular contracture
  • 32.  BRCA1/2 carriers- 53% reduction in risk of breast cancer
  • 33. Autologous flaps  pedicled flap  TRAM  LD Free flap  DIEP flap  SIEA flap Prosthetics  Silicon prosthesis  Tissue expanders
  • 34.  Several risk-reducing strategies exist  identify high-risk patients  High-risk surveillance with MRI as an adjunct to mammography  Chemoprevention  Surgical prophylaxis remains the most effective means to prevent breast cancer.