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Kara J. Milliron, MS, CGC
Certified Genetic Counselor
Breast and Ovarian Cancer Risk Evaluation Program
University of Michigan Comprehensive Cancer Center
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These slides are the property of the presenter. Do not duplicate without express written consent.
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I am a contract genetic counselor with Informed Medical
Decisions, Inc.
These slides are the property of the presenter. Do not duplicate without express written consent.
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Introduction to breast cancer pathology
Triple negative breast cancer (TNBC)
TNBC and BRCA1/2
BRCA1/2 genetic testing and the NCCN guidelines
Cases
Other genetic causes of TNBC
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Breast profile:
A Ducts
B Lobules
C Dilated section of duct
to hold milk
Invasive lobular 10%
D Nipple
Invasive ductal 80%
E Fat
F Pectoralis major muscle
G Chest wall/rib cage
Enlargement
A Normal duct cells
B Basement membrane
C Lumen (center of duct)
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 Modified
Bloom
Richardson Grade
 Scored
 Based
 Grade
on three
characteristics
o Degree of tubule
formation
o Nuclear pleomorphism
o Mitotic activity
on a scale 1-3
I
 Grade II
 Grade III
These slides are the property of the presenter. Do not duplicate without express written consent.
These slides are the property of the presenter. Do not duplicate without express written consent.
1985: Her2neu
discovered by 2
independent labs
 1987: Her2neu
amplification shown to
be a poor prognostic
factor in breast cancer
 1998: Addition of
trastuzumab proven
beneficial in Her2neu +
metastatic patients
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 ER
negative
 15%
of all invasive
breast cancers
 Risk Factors
o dx <50 years
 PR
negative
o A. American ancestry
o High BMI
o Young age menarche
o High parity
 Her2Neu
negative
o Young age of FLB
o Lack of breast feeding
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Ductal NOS
o Poorly differentiated
o High nuclear grade
o Highly proliferative
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Rare histological subtypes
Medullary
Good Prognosis
Adenoid cystic
Metaplastic
Poor Prognosis
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Estimated New Female Breast Cancer Cases by Age, US, 2011*
Age
In Situ Cases
Invasive Cases Est. TNBC (total) cases
(~15%)
< 40
1,780
11,330
1700
< 50
14,240
50,430
7564
50-64
23,360
81,970
12,296
65+
20,050
98,080
14,712
All ages
57,650
230,480
36,272
*Rounded to the nearest 10.
Source: Total estimated cases are based on 1995-2007 incidence rates from 46 states as reported by the
North American Association for Central Cancer Registries. Total estimated deaths are based on data from
US Mortality Data, 1969-2007, National Center for Health Statistics, Centers for Disease Control and
Prevention. American Cancer Society, Surveillance Research, 2011
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ACT dose dense fashion most common
TC every 3 weeks can be utilized in some patients
Platinum agents have recently emerged as drugs of interest
o One trial that treated 28 women with stage II or stage III TNBC with four
o
o
o
o
cycles of neoadjuvant cisplatin resulted in a 22% pCR rate
CALGB-40603 (NCT00861705), evaluated the benefit of carboplatin
added to paclitaxel and adriamycin plus cyclophosphamide
chemotherapy in the neoadjuvant setting.
Triple Negative Trial (NCT00532727), is evaluating carboplatin against
docetaxel in the metastatic setting.
These trials will help to define the role of platinum agents for the
treatment of TNBC.
Currently, there is no established role for adding platinum agents to the
treatment of early-stage TNBC outside of a clinical trial.
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African American
Non-African American
Pre-menopausal
39%
16%
Post-menopausal
14%
16%
Carolina Breast Cancer Study JAMA 2006
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Bassett
Coates
Gordon
Ansell
Neale
Eley
Perkins
Simon (>49 yo)
Simon (<50 yo)
Franzini
Howard
Wojcik
Yood
El Tamer
Roetzheim
Albain Premen
Albain Postmen
Polednak
Bradley
Jatoi 1995-99
Crowe
Combined
.1
.5
1
mortality hazard
5
AA Mortality Risk: 1.28 (95% CI 1.18-1.38)
(22% excess risk of death)
Newman et al, JCO 2006
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10
Higher Mortality
 Advanced Stage
Distribution
 Lower lifetime
incidence
 Younger age
distribution
 Increased risk of
adverse tumor factors
 Higher incidence of
male breast cancer
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Socioeconomic
disparities
 Delivery of Care
 Tumor biology
 Genetics
 Lifestyle &
Reproductive
Experiences
 Environmental
exposures
 Diet/Nutrition
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 60%
of breast
cancers in Ghanian
women are TNBC
 Location of many of
the slave colonies
several hundred
years ago
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 Parallels
between hereditary breast cancer
(BRCA1/2) and breast cancer in individuals with
African ancestry
o younger age distribution
o increased prevalence of ER-neg, aneuploid tumors
o higher risk of male breast cancer
 Is
African ancestry associated with a heritable
marker for high-risk breast cancer subtypes?
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How Much Breast and Ovarian
Cancer is Hereditary?
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Causes of Hereditary Breast and Ovarian
Cancer Syndrome
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BRCA1
BRCA2
Year cloned
1994
1995
Chromosome
location
17q21
13q12
5.6 kb/22 exons
10.2 kb/26 exons
# of amino acids
1, 863
3, 418
# of mutations reported
>1, 230
>1,380
Genomic DNA/coding
exons
Inheritance pattern
Autosomal
Dominant
Autosomal
Dominant
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 Breast
cancer to age 80
 Ovarian
 Male
BRCA2
50-85%
50-85%
cancer to age 80 20-60%
breast cancer
 Prostate
BRCA1
cancer
 Pancreatic
 Melanoma
cancer
up to 27%
~1%
~6%
Slight ↑
Slight ↑
Slight ↑
1.5-5%
Slight ↑
Slight ↑
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Breast cancers in BRCA1 carriers80% Triple negative
Breast cancer in BRCA2 carriers20% Triple negative
o Mutation Carrier frequency in general population 1/300-1/800
o Mutation Carrier frequency in A. Jewish population 1/40
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Gonzalez-Angula CCR 2011
o 77 unselected TNBC
o 15% incidence of BRCA1 mutation (one somatic) (12)
o 3.9% incidence of BRCA2 mutation (3)
o 9/14 had no first degree family history of cancer
o However, 22/77 or (30%), DID have a family history of breast
and ovarian cancer
o In addition 12/77 (16%) HAD a first degree relative with
breast cancer
o 6/14 found to be BRCA carriers had not been referred to genetic
counseling
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Diagnosed age < 60 y with a TNBC
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Estimated New Female Breast Cancer Cases by Age, US, 2011*
Age
In Situ Cases
Invasive Cases Est. TNBC (total) cases
(~15%)
< 40
1,780
11,330
1700
< 50
14,240
50,430
7564
50-64
23,360
81,970
12,296
65+
20,050
98,080
All ages
57,650
230,480
*Rounded to the nearest 10.
21,560
potential patients
tested for BRCA1/2
from these cases
alone
Healthcare cost
14,712 for testing
$4000 X 21,560
36,272 = $86,240, 000.00
~$107,800 to find
1 BRCA1/2
positive individual
Source: Total estimated cases are based on 1995-2007 incidence rates from 46 states as reported by the
North American Association for Central Cancer Registries. Total estimated deaths are based on data from US
Mortality Data, 1969-2007, National Center for Health Statistics, Centers for Disease Control and Prevention.
American Cancer Society, Surveillance Research, 2011
These slides are the property of the presenter. Do not duplicate without express written consent.
These slides are the property of the presenter. Do not duplicate without express written consent.
These slides are the property of the presenter. Do not duplicate without express written consent.
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46 year old G1P1 Filipino female
s/p L lumpectomy
o 1.8 cm invasive ductal carcinoma
o Triple negative
o 0/3 SLN
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Menarche: 11
FLB: 23
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s/p 4 cycles AC
s/p 2 cycles T
Carries BRCA2 mutation R3052W
Recorded 8 times in the BIC located in exon 24 of
BRCA2
Bilateral mastectomy with reconstruction is scheduled for
the near future
Plans on BSO, scheduled with Dr. Pearlman to further
discuss options
Scheduled with Dr. El Munzer to discuss risks, benefits,
and limitations of pancreatic cancer screening
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These slides are the property of the presenter. Do not duplicate without express written consent.
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51 year old G4P3SAB1 Caucasian female
s/p R lumpectomy
o 2 foci 0.3 cm and 0.7 cm invasive ductal carcinoma
o Triple negative
o 0/1 SLN
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s/p 3 cycles AC
s/p 1 cycle of Taxol, developed toxicity
s/p 15 weeks of weekly Taxotere
s/p radiotherapy
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Patient is adopted with some knowledge about family
history
BRCA1/2 genetic testing-no mutation detected
Based on negative test results, not felt to be at increased
risk for ovarian cancer
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These slides are the property of the presenter. Do not duplicate without express written consent.
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59 year old G0 Chinese female
s/p Left breast biopsy
Discrepancy in size of tumor via imaging—u/s 1.5 cm vs
MRI 3 cm
No definitive cancer surgery
Lymph nodes not sampled
Triple negative
Due to NCCN guidelines, requested BRCA1/2 genetic
testing
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BRCA1/2 genetic testing revealed a variant of uncertain
significance (VUS) BRCA1 G1157R
1st reported observation of this VUS
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dx 60's
Colon
c a nc e r
d. Alzheimer' s
~ 75
dx 50's
d. Colon
c ance r
60
d. 65
CO PD
? Lung
c a nc e r
Use d
toba cc o
69
s/p
TAH/
BSO
d. 50's
MI
73
d. 53
MI
d. 75
? Ane ury sm/
CVA/MI
d. 70
Lung
c a nc e r
Use d
toba cc o
3
41
dx 41
4
49
44
50's
50's
50's
dx 41
DC IS
d. 40's
Choke d
MR
6
20
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30
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41 year old G2P2 Caucasian female
s/p 4 cycles AC, and 3 cycles T (neo-adjuvant)
R breast cancer 2.1 X 2.4 X 2.6 cm via U/S
Triple negative
0/8 SLN
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 Patient
was found to have BRCA2 VUS N1910S
 1st observation
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Genetic counseling-what do they mean to the patient?
Does everyone agree on the interpretation?
Inconsistency between DNA diagnostic laboratories and
between countries on interpretation and reporting of
variants
In US-Myriad Genetic Laboratories alone reports and
interprets
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BRCA1/2
o ~ 7% of overall test
results
o ~ 15% of test results if of
African American
descent
o Most seen < 3 times
Few are likely to be
associated with a high
risk of disease
 BUT knowing which
ones is difficult to
ascertain
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Unfortunately, since these were the first observation of
these VUS, and there is no family history of cancer,
additional investigation at this time is not helpful.
Due to rarity of VUS, follow HBOC guidelines
BSO to be considered by both patients in the near future
once they have completed breast cancer treatment
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Another Cause of TNBC
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Autosomal recessive (i.e.
2 PALB2 mutations)
Characterized by:
o Thumb deformity
o Kidney malformation
o Small stature
o Developmental delay
o Microcephaly
o Bone marrow failure
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These slides are the property of the presenter. Do not duplicate without express written consent.
PALB2
is a low penetrence breast
cancer susceptibility gene
Encodes a BRCA2 interacting protein
Rahman et al. 2007
o Found monoallelic truncating
mutations in 10/923 (1%) familial
breast cancer families and 0/1084
(0%)controls
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These slides are the property of the presenter. Do not duplicate without express written consent.
These slides are the property of the presenter. Do not duplicate without express written consent.
 Carriers
are at a 2-3 fold increased risk of
developing breast cancer
 May confer a higher RR for male breast
cancer vs. female breast cancer
 Ovarian cancer risk not studied
 Clinical management for unaffected individuals
is based on family history
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Heikkinen et al CCR 2009
2% (19/947) of familial breast cancer patients in S.
Finland had mutations
Tumors of the PALB2 mutation carriers were more often
o triple negative
o basal-like subtype
o higher expression of Ki67
o lower expression of cyclin D1
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Increased risk for pancreatic cancer
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Is becoming more complex
o age is only a number 
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We are testing based on cancer pathology (i.e. TNBC)
We may need to test for multiple genes
This will impact
o Integration of genetic testing into diagnostic and treatment flow
o Multiple genes tested (will insurers pay?)
o ? increase the uptake of bilateral mastectomy (patients not
wanting to wait for all information before making a surgical
decision)
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Cancer risk management for those with inherited
susceptibility is a challenging and dynamic process
Consistent protocols for counseling/help manage/recontact these high risk patients
How to Contact us
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Clinic coordinator: Kara J. Milliron, MS, CGC
734.764.0107 or 734.936.6266 pager number 8881
These slides are the property of the presenter. Do not duplicate without express written consent.
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Sofia D.Merajver, MD, PhD
Celina Kleer, MD
Mark D. Pearlman, MD
Kathleen Diehl, MD
Breast Care Center
Hematology/Oncology
Surgical Oncology
Radiation Oncology
Gynecology Oncology Clinic
Radiology
Obstetrics and Gynecology
Primary Care Clinics
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Genes: The Link to Our Past—The Bridge to Our Future:
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