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DG-041 Single Dose Results

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Genetic Risk Tests for early detection of Prostate Cancer Jeff Gulcher MD PhD Chief Scientific Officer and co-Founder Decode Genetics Prostate cancer detection 27,000 ... – PowerPoint PPT presentation

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Title: DG-041 Single Dose Results


1
Genetic Risk Tests for early detection of
Prostate Cancer Jeff Gulcher MD PhD Chief
Scientific Officer and co-Founder Decode Genetics
2
Prostate cancer detection
  • 27,000 men died in 2007, African-Americans at
    higher risk for cancer and for death due to
    cancer
  • (15 years ago 40,000 deaths per year before PSA
    used )
  • Best treatment is early detection
  • We have tools for curative treatment if detected
    early
  • More emphasis needs to be made on early detection
    vs late treatment
  • The only major risk factors are ethnicity and
    family history of early prostate cancer (younger
    than 65)
  • Need new ways to focus PSA and diagnostic
    procedures to those who are highest risk

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5
Prostate cancer genetic risk markers discovery
and wide replication
  • Discovery in white populations 2500 patients vs
    20,000 controls using 300,000 markers
  • All 8 markers replicated in 4000 to 12,000 white
    patients and 30,000 white controls
  • 4 of these markers have been replicated in
    smaller numbers African-American patients (small
    collections of 150 to 500)
  • The remaining markers may not adequately tested
    in small numbers of patients may need to
    recruit more participants in these important
    studies
  • In some cases the markers which are more
    important to African-Americans are different but
    near the ones first found in whites
  • In other cases, the strongest markers for whites
    are not important for African-Americans and vice
    versa (example- the 9p21 heart attack markers do
    not impact AA risk)

6
Prostate cancer genetic risk test (deCODE
ProstateCancer)
  • Measures 8 SNP markers over 6 regions originally
    discovered by Decode and confirmed in numerous
    populations covers 70 of the genetic risk
  • The genetic risk profile ranges from 0.4 to over
    6 fold
  • 10 of the white population is at 2 fold risk
    (33 lifetime risk), 1 has 3 fold risk (49
    lifetime risk)
  • This is a risk test not determinative
  • Defines patients more likely to have more
    aggressive cancer
  • The risk profile is independent of risk due to
    family history

7
Case Study in the use of deCODE Prostate Cancer
  • 48 year old white male in good apparent health,
  • father diagnosed with localized prostate cancer
    at age 68
  • ACS guidelines recommend screening with PSA
    beginning at age 50 unless family history of
    early prostate cancer lt 65
  • deCODE Prostate Cancer results
  • Relative risk 1.88 fold compared to general
    population risk for white males.
  • Calculated lifetime risk 1.88 X 16 30
  • Modestly higher risk for aggressive vs.
    non-aggressive disease

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9
Case Study in the use of deCODE Prostate Cancer
  • High risk prompted early PSA test by primary care
  • PSA midrange normal at 2.0ng/ml
  • High risk prompted urologist to perform
    TRUS-guided biopsy
  • Positive in 3 out of 12 core biopsies 15
    volume
  • Gleason score of 6 (3/3) intermediate grade
  • Negative workup for cancer spread
  • Radical prostatectomy with nerve sparing for
    likely cure
  • Final pathology on resected prostate showed
    Gleason 7 (high-grade) in both lobes
  • Followup PSA now 0.0 (presumed cure)

10
Risk Family History
5
15 High Risk account for 30 of prostate cancers
High Risk
Family History Alone
deCODE ProstateCancer

95
Family History
Average Risk
11
Prostate cancer early detection needs for
African-Americans
  • Need larger collections of patients and controls
  • To ensure rapid translation of discoveries made
    in large studies in white to African-Americans,
    who are at even higher overall risk
  • Need to use in African-Americans the
    industrial-scale genetic approaches that have
    worked so well in whites
  • Solutions
  • Collaborate with patient organizations like PHEN
    and NMA to recruit more participants
  • Continue and expand funding for collections of
    patients and controls by medical centers
  • Combine the numerous projects at NIH and funded
    by NIH
  • Do not cut the SCOR grant program which funds
    collections
  • Begin to fund genome-wide association discovery
    projects for African-Americans (does not exist
    because large numbers of patients have not been
    collected Catch-22)
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