31
Genomic Landscape of Breast Cancer in Women of African Ancestry Olufunmilayo I Olopade, MD, FACP, OON Walter L. Palmer Distinguished Service Professor ACS Clinical Research Professor The University of Chicago

Genomic Landscape of Breast Cancer in Women of African ... · Discuss opportunities in Precision Medicine for All 2. Precision Cancer Care in the Genomic Era. ... Achieving distinction

  • Upload
    others

  • View
    1

  • Download
    0

Embed Size (px)

Citation preview

  • Genomic Landscape of Breast Cancer in Women of

    African Ancestry

    Olufunmilayo I Olopade, MD, FACP, OONWalter L. Palmer Distinguished Service Professor

    ACS Clinical Research ProfessorThe University of Chicago

  • Outline1. Introduction2. Define the genomic basis for

    inherited breast cancer3. Describe ongoing research

    integrating germline and somatic genomic research.

    4. Discuss opportunities in Precision Medicine for All

    2

  • Precision Cancer Care in the Genomic Era

    This requires genetic information for the bestrisk assessment and the best therapies

  • Breast cancer rates by race/ethnicityU.S. 2008-2012, age-adjusted

    Incidence rate, per 100,000 Mortality rate, per 100,000

  • Gene Expression Profiles in Hereditary Breast Cancer

    Hedenfalk et al., NEJM, 344:539-548, 2001

  • Medullary and atypical medullary High mitotic rate Aneuploid High proliferation fraction – high KI67 ER negative, PR negative No HER2 gene amplification Frequent Tp53 mutations BRCA1 – associated basal like breast cancers

    have the WORST outcomes African Americans have the worst overall

    breast cancer related outcomesBreast Cancer Linkage ConsortiumCrook T et al., Lancet, 1997Grushko et al. Cancer Research, 2002

    BRCA1 Tumors Have a Distinct Phenotype

  • Subgroups of Breast Cancer• Molecular subtypes

    – Estrogen receptor -- druggable target– Progesterone receptor– HER-2/neu -- druggable target– Gene expression profiling: 4 or more subtypes

    • Luminal A, luminal B, basal-like, her2-enriched

    ER PR HER-2/neu

  • Breast Cancer Subtypes Across Populations(N=482 in Nigeria & Senegal) (N=203, Ilorin, Nigeria)

    0% 20% 40% 60% 80% 100%

    Japanese (median age = 54 y)

    White in Poland (mean age = 56 y)

    White in US (postmenopausal)

    White in US (premenopausal)

    African American (postmenopausal)

    African American (premenopausal)

    Nigeria & Senegal (mean age = 45 y)

    Ilorin, Nigeria (mean age = 48 y)

    Luminal A Luminal B Her2+/ER– Basal-like Unclassified

    Huo et al. J Clin Onc 2009

    Chart1

    Japanese (median age = 54 y)Japanese (median age = 54 y)Japanese (median age = 54 y)Japanese (median age = 54 y)Japanese (median age = 54 y)

    White in Poland (mean age = 56 y)White in Poland (mean age = 56 y)White in Poland (mean age = 56 y)White in Poland (mean age = 56 y)White in Poland (mean age = 56 y)

    White in US (postmenopausal)White in US (postmenopausal)White in US (postmenopausal)White in US (postmenopausal)White in US (postmenopausal)

    White in US (premenopausal)White in US (premenopausal)White in US (premenopausal)White in US (premenopausal)White in US (premenopausal)

    African American (postmenopausal)African American (postmenopausal)African American (postmenopausal)African American (postmenopausal)African American (postmenopausal)

    African American (premenopausal)African American (premenopausal)African American (premenopausal)African American (premenopausal)African American (premenopausal)

    Nigeria & Senegal (mean age = 45 y)Nigeria & Senegal (mean age = 45 y)Nigeria & Senegal (mean age = 45 y)Nigeria & Senegal (mean age = 45 y)Nigeria & Senegal (mean age = 45 y)

    Ilorin, Nigeria (mean age = 48 y)Ilorin, Nigeria (mean age = 48 y)Ilorin, Nigeria (mean age = 48 y)Ilorin, Nigeria (mean age = 48 y)Ilorin, Nigeria (mean age = 48 y)

    Luminal A

    Luminal B

    Her2+/ER–

    Basal-like

    Unclassified

    0.6330390921

    0.1954602774

    0.0693568726

    0.0844892812

    0.0176544767

    0.6865671642

    0.0597014925

    0.0758706468

    0.118159204

    0.0597014925

    0.665

    0.107

    0.06

    0.093

    0.075

    0.574

    0.124

    0.056

    0.145

    0.101

    0.563

    0.087

    0.077

    0.16

    0.113

    0.414

    0.073

    0.084

    0.272

    0.157

    0.2821576763

    0.0248962656

    0.1493775934

    0.2634854772

    0.2800829876

    0.2047

    0.1111

    0.193

    0.2515

    0.2398

    Sheet1

    AsianEuropeanAfricanWhiteBlackNC update

    JapanWhite in PolishWhite in NCAA in NCAA in DCWest AfricaNigerianCaliforniaCaliforniaWhiteAA

    ER+ or PR+, HER2-50255216293206136118509287

    ER+ or PR+, HER2+155485225441249245

    ER-, PR-, HER2-8114369627927124174201

    ER-, PR-, HER2+55611716437266848

    793804300196372491152843581

    ER+ or PR+, HER2-63%69%54%47%55%28%78%60%49%

    ER+ or PR+, HER2+20%6%17%13%12%2%3%11%8%

    ER-, PR-, HER2-10%18%23%32%21%55%16%10.80%24.60%21%35%

    ER-, PR-, HER2+7%8%6%8%12%15%4%8%8%

    Sampling adjusted

    10841.441.5%

    7027.226.9%

    228.48.5%

    197.37.3%

    4115.715.8%

    260

    17956.355.8%

    521616.2%

    267.78.1%

    268.78.1%

    3811.311.8%

    321

    21657.457.1%

    5414.514.3%

    245.66.3%

    4612.412.2%

    3810.110.1%

    378

    29366.563.0%

    499.310.5%

    4469.5%

    4610.79.9%

    337.57.1%

    465

    Sheet1

    ER+ or PR+, HER2-

    ER+ or PR+, HER2+

    ER-, PR-, HER2-

    ER-, PR-, HER2+

    Sheet2

    Japanese (median age = 54 y)White in Poland (mean age = 56 y)White in US (postmenopausal)White in US (premenopausal)African American (postmenopausal)African American (premenopausal)Nigeria & Senegal (mean age = 45 y)Ilorin, Nigeria (mean age = 48 y)

    Luminal A63.3%68.7%66.5%57.4%56.3%41.4%28.2%20.5%

    Luminal B19.5%6.0%10.7%12.4%8.7%7.3%2.5%11.1%26%14%17%18%16%16%17%

    Her2+/ER–6.9%7.6%6.0%5.6%7.7%8.4%14.9%19.3%

    Basal-like8.4%11.8%9.3%14.5%16.0%27.2%26.3%25.2%

    Unclassified1.8%6.0%7.5%10.1%11.3%15.7%28.0%24.0%

    Luminal A502552136subtype | Freq. Percent Cum.

    Luminal B1554812-------------+-----------------------------------

    Her2+/ER–556172Luminal A | 35 20.47 20.47

    Basal-like6795127Luminal B | 19 11.11 31.58

    Unclassified1448135Basal-like | 43 25.15 56.73

    Total793804465378321260482HER2+/ER- | 33 19.30 76.02

    Unclassified | 41 23.98 100.00

    -------------+-----------------------------------

    Total | 171 100.00

    Sheet2

    Luminal A

    Luminal B

    Her2+/ER–

    Basal-like

    Unclassified

    Sheet3

    Luminal A

    Luminal B

    Her2+/ER–

    Basal-like

    Unclassified

  • Estrogen Receptor Status by RegionsRegion No. of studies ER+ (95% CI)North-eastern (Egypt, Sudan, and Libya)

    30 0.63 (0.60-0.66)

    North-western (Morocco, Algeria, and Tunisia)

    24 0.54 (0.50-0.59)

    Western (Ghana, Mali, Nigeria, and Senegal)

    13 0.35 (0.23-0.46)

    Eastern (Kenya, Uganda, Tanzania, and Madagascar)

    7 0.41 (0.33-0.50)

    Southern (South Africa) 6 0.60 (0.56-0.64)US SEER, African Americans 0.64US SEER, Caucasians 0.80

    Eng et al. Plos Med 2014

    Heterogeneity across studies can also be explained by age at diagnosis, study design (prospective, retrospective)

  • 64 yr old white woman with interval TNBC

    03/06/03 03/08/05Died 10/06

    Aggressive ER Negative Breast Cancer

  • US Supreme Court --Opening the Pandora’s Box…or closing it?

  • 45 year old diagnosed with TNBC after self palpating a mass 6 months after normal MMG

  • Why not sequence everyone’s genome?

    Adapted from Ian Foster, Computational Institute

  • Phenotypic Effect Size and Frequency of Occurrence of Cancer Susceptibility Genes

    Stadler Z et al. J Clin Oncol 2010;28:4255-4267

  • BROCA: African Americans in Chicago

    • 289 African American patients with primary invasive breast cancer and with personal or family cancer history or tumor characteristics associated with high genetic risk.

    • Sixty-eight damaging germline mutations were identified in 65 subjects (22%, 95% CI 18–28%).

    Breast Cancer Res Treat. 2015 Jan;149(1):31-9.

  • Fine-mapping of known susceptibility lociCases Controls P value

    Age, mean ± SD 48.0 ± 12.0 47.2 ± 17.2 0.08

    Age < 50 yrs, n (%) 878 (58.4%) 799 (57.9%) 0.76

    % of African ancestry

    Nigerian 0.980 ± 0.012 0.981 ± 0.010 0.08

    Barbadian 0.856 ± 0.104 0.857 ± 0.098 0.93

    African American 0.776 ± 0.135 0.787 ± 0.120 0.10

    Baltimore 0.807 ± 0.133 0.795 ± 0.122

    Pennsylvania 0.780 ± 0.134 0.793 ± 0.112

    Chicago 0.773 ± 0.141 0.796 ± 0.115

    Northern California 0.758 ± 0.125 0.763 ± 0.131

  • P = 0.42 P = 5.0E-15

    .7

    1

    1.5

    2

    2.5

    12-19 20-21 22-23 24-31 1-4 5 6 7-12

    22 Index Markers 8 Best Markers in African Ancestry

    Odd

    s R

    atio

    , 95%

    CI

    Risk Allele Count

    Zheng, et al. Carcinogenesis 2013

  • GWAS consortia of breast cancer in women of African Ancestry

    Study consortium Cases Controls

    AABC (discovery phase) 2120 1917

    ROOT (discovery phase) 1657 2028

    AMBER (validation phase) 2754 3698

    Total 6522 7643

    ER+ 2933

    ER- 1876

  • Somatic Signatures in whole exome data

    | Presentation Title | Presenter Name | Date | Subject | Business Use Only21

  • Significantly mutated genes in breast cancer

    WABCS Update | OTR Lab Meeting | July 16, 2015

    TCGA consortium, Nature 2012

    22

  • Hereditary Breast Cancers (High risk)

    Breast Imaging

    Gierach GL et al. Relationships between computer-extracted mammographic texture pattern features and BRCA1/2 mutation status: a cross-sectional study. Breast Cancer Res. 2014;16(424):1-16.

    All Breast Cancers (Average risk)

    BRCA1/2

    Routine Mammography

    Genetic risk assessment,

    advanced screening modalities

    Radiogenomics classifier

  • Angelina Jolie•Not all women need risk reducing mastectomies

    •BRCA1+ women need risk reducing oophorectomies

    •BRCA-associated cancers benefit from Parp Inhibitors

    • Positive trials in ovarian cancer, prostate cancer and breast cancer etc

  • $700mm Center for Care and Discovery

    “Devoted to complex specialty care, with a focus on cancer and advanced surgical programs”

    “Major advances will be driven by discoveries in genomics and personalized medicine”

  • • More effectively using genomics for:

    • Preventative care

    • Treatment

    The “Forefront” of Oncology

    27

    • Multidisciplinary Collaboration

    • Improved BiospecimenCollection and Repository System

    • Clinical Trial Awareness

    • Efficient Patient Recruitment

    • Clinical Trial Participation

    Cutting Edge Research

    1.

    Achieving distinction in cancer genomics and personalized care requires:

    Personalized Care3.

    Innovative Clinical Trials

    2.

  • Final Thoughts• Physician Scientists can accelerate

    discovery and translation of research that benefit patients 21st Century Medicine is interdisciplinary, patient

    centered, community based and networked Diverse team of investigators --- basic science,

    clinical trials, behavioral science, population science, policy, implementation science and health economics etc.

    Address global burden of disease – cancer predicted to be leading cause of death globally

    Education mission is robust - prepare a diverse workforce to serve diverse populations

    Leverage public private partnerships to accelerate progress

  • Univ. ChicagoOlopade LabDezheng HuoNkem ChinemeDominique SighokoYonglan ZhengGalina KhramtsovaLise Sveen

    IGSB/White LabKevin WhiteJason GrundstadJason PittJigyasa Tuteja

    Dept. Health StudiesDezheng Huo

    Acknowledgement

    Univ. IbadanDept. Ob/GynOladosu OjengbedeOmobolanle OyedeleStella OdedinaImaria Anetor

    Dept. PathologyAbideen OluwasolaMustapha Ajani

    Dept. SurgeryTemidayo OgundiranAdeyinka AdemolaKelechi WilliamsChibuzor Afolabi

    IAMRATChinedum BabalolaAbayomi OdetundeIfeanyi NwosuJide OkedireOdunayo Akinyele

    LASUTHJohn ObafunwaAbiodum PopoolaOlorunde IfeoluwaVictor AderojuAnne AyodeleMobolaji OludaraNasiru IbrahimAyodele SanniFelix SanniEsther Obasi

    NovartisDimitris PapoutsakisJordi BarretinaScott Mahan

    University of WashingtoonSeattleMC KingTom Walsh

  • GWAS Acknowledgement

    Dezheng HuoYonglan ZhengStephen HaddadSong YaoYoo-Jeong HanFrank QianTemidayo O. OgundiranClement AdebamowoOladosu OjengbedeAdeyinka G. FalusiWilliam BlotWei ZhengQiuyin CaiLisa SignorelloKatherine L. NathansonSusan M. DomchekTimothy R. Rebbeck

    Julie R. PalmerEdward N. RuizLara SuchestonJeannette BensenMichael S. SimonAnselm HennisBarbara NemesureSuh-Yuh WuM. Cristina LeskeStefan AmbsEric GamazonLin ChenKathyrn L. LunettaNancy J. CoxAndrew F. OlshanChristine B. AmbrosoneYe Feng

    Christopher A. HaimanEsther M. JohnLeslie BernsteinJennifer J. HuRegina G. ZieglerSarah NyanteElisa V. BanderaSue A. InglesMichael F. PressSandra L. DemingJorge L. Rodriguez-GilStephen J. ChanockLaurence N. Kolonel

  • Acknowledgement

    TCGA breast cancer analytical working group•Dezheng Huo, U of Chicago•Jason Pitt, U of Chicago•Shengfeng Wang, U of Chicago•Chuck Perou, U of North Carolina•Katherine A. Hoadley, U of North Carolina•Hai Hu, Windber Research Institute•Jianfang Liu, Windber Research Institute•Suhn Kyong Rhie, U of South California•Peter Laird, Van Andel Institute•Andrew D. Cherniack, Broad Institute

    Hem/Onc Seminar 2016

    Genomic Landscape of Breast Cancer in Women of �African AncestrySlide Number 2Slide Number 3Breast cancer rates by race/ethnicity�U.S. 2008-2012, age-adjustedSlide Number 5Slide Number 6Slide Number 7Slide Number 8Subgroups of Breast CancerBreast Cancer Subtypes Across Populations�(N=482 in Nigeria & Senegal) (N=203, Ilorin, Nigeria)Estrogen Receptor Status by RegionsSlide Number 12US Supreme Court --Opening the Pandora’s Box�…or closing it?Slide Number 14Slide Number 15Phenotypic Effect Size and Frequency of Occurrence of Cancer Susceptibility GenesSlide Number 17Fine-mapping of known susceptibility lociSlide Number 19GWAS consortia of breast cancer in women of African AncestrySomatic Signatures in whole exome dataSignificantly mutated genes in breast cancerBreast ImagingSlide Number 24A Modified Definition of Precision MedicineSlide Number 26The “Forefront” of OncologyFinal Thoughts�Slide Number 29GWAS AcknowledgementAcknowledgement