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![Page 1: Laura J. Van ‘t Veer Helen Diller Family Comprehensive Cancer Center University of California, San Francisco Biology of disease Who is at risk for what.](https://reader034.fdocuments.us/reader034/viewer/2022042821/56649ceb5503460f949b6cbd/html5/thumbnails/1.jpg)
Laura J. Van ‘t VeerHelen Diller Family Comprehensive Cancer Center
University of California, San Francisco
Biology of disease
Who is at risk for what type of breast cancer and how does type affect outcome
BOP breast course Nov 2010
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Kaplan-Meier Survival Curves
Who gets what type of breast cancer?Which breast cancers return?
Breast Cancer - Survival
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Disease Biology
• Genetic make-up of individual
• Biology of screen-detected cancers and of intervalcancers
• Biology informs need for systemic treatment
- who is at risk for what type of disease- does type affect outcome- how can type of detection inform management
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Who is at risk for what type of disease
Opportunities for prevention
Opportunities for management
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rs number Gene Chromo-some
MAF Per allele OR
P (trend test)
rs1045485 CASP8 2q 0.13 0.88 1.1 x 10–7
rs2981582 FGFR2 10q 0.38 1.23 2.0 x 10–76
rs1219648 FGFR2 10q 0.39 1.32 1.1 x 10–10
rs10941679 5p12 0.24 1.19 2.9 x 10–11
rs3803662 TNRC9 16q 0.25 1.20 10–36
0.27 1.28 5 x 10–19
rs13387042 2q34 0.50 1.20 1.3 x 10–13
rs13281615 8q24 0.40 1.08 5 x 10–12
rs889312 MAP3K1 5p 0.28 1.13 7 x 10–20
rs3817198 LSP1 11p 0.30 1.07 3 x 10–9
Familial aggregation of breast cancer
5%(?) CHEK2 1100delC*
Multiple low-penetrance alleles (polygenic model)
25% BRCA1/2
4.7% SNPs
Breast cancer susceptibility loci
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rs number Gene Chromo-some
MAF Per allele OR
P (trend test)
rs1045485 CASP8 2q 0.13 0.88 1.1 x 10–7
rs2981582 FGFR2 10q 0.38 1.23 2.0 x 10–76
rs1219648 FGFR2 10q 0.39 1.32 1.1 x 10–10
rs10941679 5p12 0.24 1.19 2.9 x 10–11
rs3803662 TNRC9 16q 0.25 1.20 10–36
0.27 1.28 5 x 10–19
rs13387042 2q35 0.50 1.20 1.3 x 10–13
rs13281615 8q24 0.40 1.08 5 x 10–12
rs889312 MAP3K1 5p 0.28 1.13 7 x 10–20
rs3817198 LSP1 11p 0.30 1.07 3 x 10–9
Recent breast cancer susceptibility loci - SNPs
Easton et al; Cox et al; Stacey et al; Hunter et al
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Association of 10 susceptibility loci with tumor subtypes
Broeks et al, BCAC, submitted
Triple negative
ER+PR+Her2-
ER+PR+Her2+
negative positive association(prevents) (increases)
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N total = 1370
Breast cancer outcome: Example rs3803662 in TNRC9Second Breast Cancer Risk
Variant allele (homozygous carriers)
in BOSOM breast cancer series
Adjusted HR (95% CI)
2.7 (1.7-4.3)
rs3803662 in TNRC9: increase of contralateral breast cancer risk
Ongoing:
Validation in BCAC series (studies with follow-up data)
Same analyses for other breast cancer risk-related SNPs
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Breast cancer outcome: MDM2 SNP309 *TP53 R72P
MDM2 SNP309 (G = variant allele)
GG
GT
TT
TP53 R72P ‘wildtype’
TP53 R72P ‘variant allele’
SNP-SNP interaction effect on survival:
MDM2 SNP309 and TP53 R72P variants combined: 7% worse survival (p<0.05)
also if adjusted for known prognostic factors
Schmidt et al Cancer Res 2007N total =3739
in BCAC breast cancer series
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Schmidt et al. JCO 2007
Breast cancer outcome: CHEK2 1100delC
Contralateral breast cancer riskHR (95%CI) 2.1 (1.0-4.3)
Recurrence-free survivalHR (95%CI) 1.7 (1.2-2.4)
Breast cancer-specific survivalHR (95%CI) 1.4 (1.0-2.1)
CHEK2 1100del C carrier:
worse breast cancer outcome
Treatment interaction?
Interaction with SNPs?
Tumor characteristics?
Ongoing data collection and analyses in BOSOM and pooled BCAC series
in BOSOM breast cancer series
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Biology informs need of systemic treatment
Opportunities to reduce over- and under-treatment
Effect on morbidity
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Kaplan-Meier Survival Curves
Which breast cancers return?
Breast Cancer - Survival
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Of 100 women with breast cancer (stage 1/2)
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…………~25% will develop a recurrence
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………..75% of all patients is treatedwith chemotherapy
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So, overall 50% of patients receive toxic chemotherapy of which they do not benefit,
but may suffer the toxic side-effects
Can we do better?
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Tumor samples of known clinical outcome
No distant metastasesgroup
Unbiased full genome gene expression
analysis
70 prognosis genes
Tu
mo
r s
amp
les
Distant metastasesgroup
Metasta
ses: wh
ite=
+
Prognosis reporter genes
b
Development of 70 gene
MammaPrint
Nature, 2002
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Multi Gene Expression Profilesin Clinical Practice
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Clinical Utility MammaPrint
Prospective study implementing MammaPrint, 2003-2006PIs Sabine Linn, Marc van de VijverSponsor: Dutch Health Insurance Council
Bueno et al, Lancet Oncol, 2007, Knauer et al, SABCS 2008 #1084
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Discordant cases MammaPrint signature versus Guidelines The Netherlands and Adjuvant-on-line
~30 % discordant cases led in ~20% to adapted treatment advise
Bueno et al, Lancet Oncol, 2007, Knauer et al, SABCS 2008 #1084
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Biology of screen detected cancers
Method of detection may inform management
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US general population screening data from SEER 1973-2005
Age-adjusted incidence breast cancer by Stage at diagnosis
Distant
In SituRegional
Localized
-> Screening era
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threshold set with 0% false negatives
70 Gene Prognosis SignatureSupervised analysis on n=78 tumors, >96% adjuvantly untreated
van´t Veer et al., Nature 415, p. 530-536, 2002
70 significant prognosis genes
Tum
or s
ampl
es
Nature, (2002)
threshold 2ultra-low
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Biology of Screen-detected CancersAge 49-60
Screen detected cancers show increase in ultra-low risk cancers
P<0.001
Pre-screening n=143, sreen-detected n=73
12%
30%MammaPrint
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