Carcinome du sein Biologie moléculaire. Thomas McKee Service de Pathologie Clinique Genève

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Transcription:

Carcinome du sein Biologie moléculaire Thomas McKee Service de Pathologie Clinique Genève

Pathology Diagnostic Prognostic information Predictive information The information provided depends on the available technology

Histology alone Breast cancer types

Breast Cancer One disease or many WHO classification

Ductal Lobular Medullary Mucinous

Histology alone Breast cancer types Tumor grade

Breast Cancer one disease or many Grading Bloom-Richardson Bloom-Richardson (BR) Score Frequency of cell mitosis Tubule formation Nuclear pleomorphism Bloom-Richardson Grade Low grade = BR score 3 5 = grade 1 Intermediate grade = BR score 6, 7 = grade 2 High grade = BR score 8, 9 = grade 3

ARCHITECTURE Score 1 Score 3 Score 2

Histology alone Breast cancer types Tumor grade Tumor stage

TNM Criteria T = Primary Tumor Tis = carcinoma in situ T1 = less than 2 cm in diameter T2 = between 2 and 5 cm in diameter T3 = more than 5 cm in diameter T4 = any size, but extends to the skin or chest wall N = Regional Lymph nodes N0 = no regional node involvement N1 = metastasis to movable same side axillary nodes N2 = metastasis to fixed same side axillary nodes N3 = metastasis to same side internal mammary nodes M = Distant Metastasis M0 = no distant metastasis M1 = distant metastasis

Breast Cancer Staging/Prognosis Stage TNM category 5 yr survival Recurrence free at 10 yrs 0 TisN0M0 99% 98% I T1N0M0 (all stage I) 92% 80% T<1 cm 90% T>1-2 cm 80-90% IIA T0N1M0;T2N0M0 82% 60-80% T1N1M0 50-60% IIB T3N0M0 65% 30-50% IIB T2N1M0 5-10% IIIA T0-2N2M0;T3N1-2M0 47% 10-40% IIIB T4N1-2M0; 44% 5-30% IIIC TanyN3M0 15-20% IV TanyNanyM1 14% <5%

Histology alone Breast cancer types Tumor grade Tumor stage Immunohistochemistry Hormone receptors

HE Presque 70% de carcinomes expriment les récepteurs hormonaux Estrogen receptor Progesterone receptor

Allred Immunohistochemistry Score Proportion score (0 1 1/100) (2 1/10) (3 1/3) (4 2/3) (5 1) Intensity score 0 = negative 1 = weak 2 = intermediate 3 = strong Total score = proportion score + intensity score (range 0, 2 8) Reprinted from Allred D, et al. Mod Pathol. 1998;11:155-168, with permission from Nature Publishing Group.

Histology alone Breast cancer types Tumor grade Tumor stage Immunohistochemistry Hormone receptors FISH/CISH HER-2

HER-2 The gene HER2/neu (ERBB2) is found on chromosome 17 (17p21) It is amplified in 10-20% of breast cancers. Breast cancers with ERBB2 amplification are more aggressive and have a worse prognosis than the average Targeted treatments are available trastuzumab

HER2 Testing Result Category IHC Score HER2 Protein Expression Testing Method FISH Score HER2 Gene Amplification Positive 3+ HER2/CEP17 ratio >2.2 Or Average gene copy number > 6 Equivocal 2+ HER2/CEP17 ratio 1.8-2.2 Or Average gene copy number 4-6 Negative 0-1+ HER2/CEP17 ratio < 1.8 Or Average gene copy number < 4 Defined as uniform intense membrane staining of >30% of invasive tumor cells

HER2 Testing HER2 analysis must be performed on the invasive component of breast cancer since HER2 overexpression and/or amplification is frequently increased in situ Equivocal results require additional action Equivocal Samples IHC FISH Confirm by FISH analysis of original sample Counting additional cells Or Repeating FISH

Immunohistochemistry: 1+

Immunohistochemistry: positive (3+)

FISH normal

FISH amplified

FISH amplified

HER-2 Problems 1. Heterogeneity

HER-2 Problems 1. Heterogeneity Solution selon ASCO Take an average report >2< And add to the report with tumor microheterogeneity

HER-2 Problems 1. Heterogeneity Solution selon ASCO Take an average report >2< with tumour microheterogeneity 2. Aneuploidy Additional or missing chromosomes

HER-2 Problems 1. Heterogeneity Solution selon ASCO Take an average report >2< with tumour microheterogeneity 2. Aneuploidy Solution Count the total HER2 signals, if more than 6 per cell, report as amplified

Does chromosome 17 centromere copy number predict polysomy in breast cancer? A fluorescence in situ hybridization and microarray based CGH analysis The Journal of Pathology Volume 219, Issue 1, pages 16-24, 8 MAY 2009 DOI: 10.1002/path.2574 http://onlinelibrary.wiley.com/doi/10.1002/path.2574/full#fig1

Histology alone Breast cancer types Tumor grade Tumor stage Immunohistochemistry Hormone receptors FISH/CISH HER-2 Expression profiling Diagnosis tumor typing

Breast cancer subtypes

Reproducibility of microarrays 295 breast cancers Agilent 24K microarrays 3 single sample predictors described by Perou and/ or Sorlie

Histology alone Breast cancer types Tumor grade Tumor stage Immunohistochemistry Hormone receptors FISH/CISH HER-2 Expression profiling Diagnosis tumor typing Prognosis

Commercially available prognostic multigene signatures for breast cancer

Oncotype DX (21-gene signature) ER+/ LN -/ Tamoxifen treated paients Proliferation Ki67 STK15 Survivin CCNB1 MYBL2 Invasion MMP11 CTSL2 CD68 BAG1 GSTM1 BAG1 CD68 Recurrence score Low risk RS 18 Intermediate risk 18>RS<31 High risk RS 31 HER2 GRB7 HER2 GSTM1 Oestrogen ER PGR BCL2 SCUBE2 Reference ACTB GAPDH RPLPO GUS TFRC

Importance of proliferation genes in prognostic signatures

Gene expression profiling: Does it add predictive accuracy to clinical characteristics in cancer prognosis? Daniela Dunkler a, d, Stefan Michiels b, c, d, Michael Schemper Explained variation in % Model without predictors 0 Standard error Model with clinical characteristics 16 ±5 Model with gene classifier 12 ±4 19 ±5 Model with clinical characteristics and gene classifier Gain by adding gene classifier to clinical characteristics 3 Clinical characteristics ER status, number of ln metastatic, histological grade

Histology alone Breast cancer types Tumor grade Tumor stage Immunohistochemistry Hormone receptors FISH/CISH HER-2 Expression profiling Diagnosis tumor typing Prognosis High throughput sequencing Personnalized medecine???

High Througput Sequencing Standard Sanger sequencing 600-1000 bp/run High throughput Roche Illumina Ion Torrent 6 600 X 10 bp per run

And Sequencing approaches. Cosmic database

Cancer genome landscapes. L D Wood et al. Science 2007;318:1108-1113 Published by AAAS

Somatic rearrangements observed in six of the twenty-four breast cancer samples screened. PJ Stephens et al. Nature 462, 1005-1010 (2009) doi:10.1038/nature08645

Tumour evolution inferred by single-cell sequencing Nicholas Navin1,2, Jude Kendall1, Jennifer Troge1, Peter Andrews1, Linda Rodgers1, Jeanne McIndoo1, Kerry Cook1, Asya Stepansky1, Dan Levy1, Diane Esposito1, Lakshmi Muthuswamy3, Alex Krasnitz1, W. Richard McCombie1, James Hicks1 & Michael Wigler1 Comparison of SK-BR-3 single cells to millions. N Navin et al. Nature 000, 1-5 (2011) doi:10.1038/nature09807

Sequencing of 50 breast cancer genomes all ER pos Ellis, Straton et al Genes PI3Kinase 40% TP53 20% MAP3K1 10% ATR 10% MyST3 10% Others <5% % of cancers harbouring mutations Suggests that there is much more heterogeneity that suggested by the expression profiling data

Does chromosome 17 centromere copy number predict polysomy in breast cancer? A fluorescence in situ hybridization and microarray based CGH analysis The Journal of Pathology Volume 219, Issue 1, pages 16-24, 8 MAY 2009 DOI: 10.1002/path.2574 http://onlinelibrary.wiley.com/doi/10.1002/path.2574/full#fig2

Breast Cancer Epidemiology: Breast cancer is the most common lethal neoplasm in women. The incidence varies among different populations 1 out of 8 women will have BC in her life-time. ~ 25 percent of women with cancer have BC. 0,5-1 % of all breast cancer cases occur in men.