pam50/prosigna®€¦ · prat et al. bcrt 2012; updated analysis unpublished pcr to sequential...
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PAM50/PROSIGNA®
Aleix Prat, MD PhD
Medical Oncology Dept.,
Hospital Clínic, Univ. of Barcelona
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Disclosures / COI
• Uncompensated advisory role for Nanostring Technologies
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Predicting…
Biology
Prognosis Treatment benefit
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Predicting…
Biology
Prognosis Treatment benefit
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Luminal A
Normal Breast Basal-like Luminal B
Claudin-low HER2-enriched Intrinsic Subtypes Perou et al., Nature 2000
Sorlie et al., PNAS 2001
Sorlie et al., PNAS 2003
Hu et al., BMC Genomics 2006
Herschkowitz et al., GB 2007
Cheang et al. JNCI 2008
Parker et al., JCO, Feb 2009
Prat et al., BCR 2010
Nielsen et al., CCR 2010
Cheang et al., CCR 2012
Prat et al. Ann Oncol 2012
Chia et al., CCR 2012
Prat et al. BCRT 2012
TCGA Nature 2012 / Cell 2014
Prat et al. JCO 2013
Martín et al. BRCT 2013
Prat et al. Oncologist 2013
Prat et al. CCR 2014
Gnant et al. Annals Oncol 2014
Rel
apse
Fre
e-S
urv
ival
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Hoadley et al. Cell 2014 BASAL-LIKE
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2013 St Gallen International Expert Consensus
Quote: “The Panel recognized the superior accuracy and reproducibility of multi-gene molecular assays”.
Goldhirsch et al. Ann Oncol 2013 Cheang et al. JNCI 2009
Endocrine Therapy (chemo in selected cases)
Endocrine + Chemo (most)
Endocrine+ Chemo + anti-HER2
Chemo + anti-HER2
Chemo
14-20%
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Prospective study of the impact of the PAM50 assay on adjuvant clinical decision-making in an unselected
population of women with ER+, HER2-negative, node-negative breast cancer: a GEICAM study
Martín et al. Curr Med Res Opin 2015
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9 (60%) ROR-low and 6 (40%) ROR-interm
2 (50%) ROR-interm and 2 (50%) ROR-high
Concordancia = 42/64 = 65.6%
Translational Genomics Group
FDA 510(k)
Local IHC vs.
Basal Her2E LumA LumB
N 0 0 22 4 26
% 0% 0% 85% 15% 100%
N 2 1 15 20 38
% 5% 3% 39% 53% 100%
N 2 1 37 24 64
% 3% 2% 58% 38% 100%Total
LumB
LumA
IHC
TotalPROSIGNA
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Analytical reproducibility of the PAM50 breast cancer intrinsic subtyping test and nCounter® analysis system using formalin-fixed
paraffin-embedded (FFPE) breast tumor specimens
Reproducibility from Tissue • N=43 FFPE / 3 testing sites • Intrinsic subtype: 97% concordance
• For ROR, 90% concordance
• ROR SD = 2.9
Precision from RNA • N=43 RNAs / 3 testing sites • Intrinsic subtype, 100% concordance
• For ROR, 100% concordance
• Site-to-site or operator-to-operator <1% of variance
• ROR SD = 0.67
Torsten et al. BMC Genomics 2014
GEICAM Study: 190 samples SUBTYPE CONCORDANCE (95%)
(Kappa = 0.89)
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Predicting…
Biology
Prognosis Treatment benefit
Tumor size
Nodal status
Tumor size
Nodal status
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PAM50 Generates an Risk Of Relapse (ROR) Score Specific to Each Patient
• Intrinsic subtype + Proliferation score + Tumor size. • “Training cohort”:
– Patients with tumors representing all subtypes. – Pre (30%) and post-menopausal patients. – None received adjuvant systemic therapy.
Parker et al. JCO 2009; Nielsen et al. CCR 2010
Patient expression
profile
PAM50 centroids
Pearson’s correlation to centroids
Proliferation score Tumor size
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ATAC study
Postmenopausal
women with invasive
BC (N=9366)
Tam alone
(N=3116)
Arimidex alone
(N=3125)
Tam + Arimidex
(N = 3125)
TransATAC study
(N=1125 blocks)
ABCSG-8 study
Post-menopausal
women with HR+
BC (N=3714)
Tamoxifen
(N=1849)
Anastrozole
(N=1865)
ABCSG-8 study
(N = 1478 blocks)
Tam
2-years 3 years
PAM50 (PROSIGNA®) Validation Studies
JNCI 2009
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Patient Report
Paciente Postmenopáusica PS 0 Tumor de 1.6 cm. RE 90%, RP 40%, Ki67 20%, HER2-negativo pT1cN0M0 LumA LumB
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JNCI 2013
• The ROR score was the strongest molecular prognostic factor in the late follow-up period, whereas IHC4 and OncotypeDX RS were only weakly prognostic in this period.
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Ivana Sestak
Jack Cuzick, Mitch Dowsett, Martin Filipits, Peter Dubsky, J. Wayne Cowens,
Sean Ferree, Carl Schaper, Christian Fesl, Michael Gnant
Centre for Cancer Prevention, Wolfson Institute of Prevention Medicine, Queen Mary University, London, UK
Academic Department of Biochemistry, Royal Marsden Hospital, London, UK
Austrian Breast and Colorectal Cancer Study Group, Vienna, Austria
Department of Surgery and Comprehensive Cancer Centre, Medical University of Vienna, Vienna, Austria
NanoString Technologies, Seattle, WA, USA
MyRAQA, Redwood Shores, CA, USA
Prediction of late distant
recurrence after 5 years of
endocrine treatment: A combined analysis of 2137 patients from the ABCSG-8
and transATAC studies using the PAM50 Risk of
Recurrence (ROR) score
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Risk groups – ROR score HR (95% CI)
Low (N=1183 (55.4%)) -
Intermediate (N=538 (25.2%)) 3.26 (2.07-5.13)
High (N=416 (19.5%)) 6.90 (4.54-10.47)
2.4%
16.6%
8.3%
0
5
10
1
5
20
5 6 7 8 9 10 Follow-up time [years]
Low
Intermediate
High
Dis
tant
recurr
ence (
%)
0
5
10
1
5
20
Sestak et al. SABCS 2013 and JCO 2015
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PAM50 in First-line HR+/HER2-neg Metastatic Breast Cancer
PFS following Letrozole monotherapy (n=644)
unpublished data
0 10 20 30 40
0.0
0.2
0.4
0.6
0.8
1.0
Pro
ba
bili
ty o
f Eve
nt
high
low
med Log Rank p=1.08e-05
0 10 20 30 40
0.0
0.2
0.4
0.6
0.8
1.0
Pro
ba
bility o
f E
ve
nt
LumA
LumB
Basal
Her2 Log Rank p=1.1e-07
SUBTYPE ROR
months months
LumA
LumB
Basal
Her2
Independent of age, visceral metastasis, prior endocrine therapy, performance status
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Predicting…
Biology
Prognosis Treatment benefit
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Multivariable Analysis (n=957) Multivariable Analysis (n=508) Variables N pCR rate OR Lower 95% Upper 95% p-value OR Lower 95% Upper 95% p-value
Age - - 1.0 0.97 1.00 0.178 1.00 0.97 1.02 0.749
Tumor size T0-T2 584 24% 1.0 - - - 1.0 - - - T3-T4 369 12% 0.6 0.50 0.84 0.001 0.5 0.30 0.81 0.005
ER IHC Positive 507 11% 1.0 - - - 1.0 - - - Negative 442 37% 1.8 0.99 3.34 0.052 1.3 0.61 2.58 0.533
PR IHC Positive 408 12% 1.0 - - - 1.0 - - - Negative 539 33% 1.1 0.65 1.89 0.716 0.8 0.40 1.51 0.463
HER2 STATUS Negative 841 22% 1.0 - - - 1.0 - - - Positive 93 35% 1.3 0.64 2.51 0.492 2.1 0.90 4.88 0.087
Grade 1 50 7% - - - - 1.0 - - - 2 285 13% - - - - 0.70 0.17 2.85 0.62
3 306 32% - - - - 1.51 0.35 6.50 0.58
Nodal status N0 157 18% - - - - 1.0 - - - N1 244 21% - - - - 0.70 0.17 2.85 0.62
N2 66 19% - - - - 1.51 0.35 6.50 0.58
N3 41 26% - - - - 1.50 0.37 6.40 0.17
PAM50 Luminal A 293 6% 1.0 - - - 1.0 - - - Luminal B 174 16% 3.3 1.72 6.44 <0.001 4.5 1.71 11.75 0.002
Basal-like 313 37% 6.1 2.94 12.66 <0.001 8.3 2.74 24.85 <0.001
HER2-E 99 38% 6.1 2.75 13.38 <0.001 13.2 4.50 38.50 <0.001
Prat et al. BCRT 2012; updated analysis unpublished
pCR to sequential anthracycline and paclitaxel/exabepilone-based regimens (N=957)
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PEPI of 0 (best prognostic group) was highest in the LumA vs. LumB (27.1% v 10.7%; P = 0.004)
J Clin Oncol 2011
LumA LumB HER2E
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LumA LumB
HER2E Basal-like
Association between breast cancer subtypes and response to neoadjuvant anastrozole
Steroids 2011
Anita K. Dunbier, Helen Andersona, Zara Ghazoui, Janine Salter, Joel S. Parker, Charles M. Perou, Ian E. Smith, Mitch Dowsett
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The Oncologist 2013;18:123–133
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Take-home messages
• Intrinsic biology (Luminal A and B, HER2-enriched and Basal-like)
captures the vast majority of the biological diversity in breast cancer.
• However, current IHC-based definitions of intrinsic subtypes are
suboptimal and the gold-standard is, in my opinion, PAM50.
• The assay is reproducible across labs and works in FFPE core biopsies
(i.e. primary tumors and metastatic tissues).
• Intrinsic subtyping and ROR, together with tumor size and nodal status,
can help identify patients:
• That do not need adjuvant polychemotherapy due to their low risk
of relapsing distantly (<10% at 10 years).
• That do not need adjuvant endocrine therapy beyond 5 years due
to their low risk of relapsing between period years 5-10 (<5% at 10
years).
• In HR+/HER2-negative disease, intrinsic subtyping at diagnosis before
neoadjuvant therapy or in first-line metastatic setting, can help decide
whether to begin with endocrine therapy or chemotherapy.
• In metastatic TNBC, distinguishing Basal-like vs. not can help predict
benefit from docetaxel vs. carboplatin.
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University of North Carolina, NC, USA
Chuck Perou Lisa Carey Joel S. Parker
GRANT SEOM PARA FORMACION EN INVESTIGACION TRASLACIONAL
GEICAM, Spain
Miguel Martín Eva Carrasco Rosalía Caballero Maribel Casas
Acknowledgements
Patricia Galván Maria Vidal Ana Vivancos Javier Cortés Josep Tabernero Vicente Peg Santiago Ramon y Cajal
CAREER CATALYST GRANT FROM SUSAN G KOMEN FOUNDATION
SOLTI, Spain
Eva Ciruelos Lorena de la Peña Josep Vazquez José Baselga
Barbara Adamo Montse Muñoz Imma Alonso Blanca Farrús Pedro Fernández