Personalized Medicine for Triple Negative Breast Cancer - New Dimensions in Therapeutic Individualization



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Personalized Medicine for Triple Negative Breast Cancer - New Dimensions in Therapeutic Individualization Bryan P. Schneider & Milan Radovich Medicine & Medical Molecular Genetics Indiana University School of Medicine

AT LEAST THREE types of breast cancer TNBC Schneider, et al CCR, 2008

The inability to define is a bad start Blond hair: negative Brown eye: negative Tall: negative TRIPLE NEGATIVE BREAST CANCER (ER-, PR-, HER2-)

TNBC Clinical Characteristics Risk Factors: Young African American BRCA carrier >3 children First birth <26 Relapse Pattern: Higher risk Early timing More visceral & CNS (46%) Dent et al; CCR 2007 n bone viscera TNBC 79 13% 74% ER+ 123 39% 54% HER2+ 78 7% 81% Liedtke et al; JCO 2008

A link between TNBC and tumors in those who carry a BRCA mutation Most BRCA-1 carriers develop TNBC Sporadic TNBC: Phenotypic similarity to BRCA-1 Patient & tumor characteristics Gene expression similarities/aberrant DNA repair BRCA dysfunction: BRCA-ness Similarities may be important! Mechanism of development Therapeutic strategies

Basal-like breast cancer and BRCA1 Most BRCA1 carriers get basal-like breast cancers Shared characteristics with sporadic basal-like: BRCAness Basal-like BRCA 1 Sorlie, PNAS 2003

Standard cytotoxic therapeutics for TNBC Traditional chemotherapy remains the standard of care Traditional chemotherapy is relatively more important Some respond VERY well to chemotherapy others do not Is TNBC really one disease? Taxanes Anthracyclines Vinorelbine Gemcitabine Capecitabine Ixabepilone

TNBC targeted therapies Treatment Target Rationale/evidence Studies Platinating agents DNA: inter-strand breaks *defective DNA repair *in vitro chemo-sensitivity in BRCA-1 *neoadjuvant DFCI *CALGB 40603 Anti-VEGF VEGF over-expression of VEGF *positive phase III trial (unplanned subgroup) PARP-1 inhibitors PARP-1 *over-expression *in vitro sensitivity *positive randomized phase II trial *accrued phase III

Randomized phase II trial of PARPi BSI-201: Metastatic TNBC (n=120) Gemcitabine Carboplatin 21 day cycle Gemcitabine Carboplatin BSI-201 Gem/carbo (n=44) Gem/carbo/BSI (n=42) P-value ORR 7 (16%) 20 (48%) 0.002 CBR 9 (21%) 26 (62%) 0.0002 CBR= CR +PR +SD 6mo

ASCO-Plenary; 2009 PARP inhibitor: Overall Survival BSI-201 + Gem/Carbo (n = 57) Median OS = 9.2 months Gem/Carbo (n = 59) Median OS = 5.7 months P = 0.0005 HR = 0.348 (95% CI, 0.189-0.649) O Shaughnessy et al

Finding new ways to attack triple negative breast cancer (next generation sequencing)

The Transcriptome DNA RNA Protein

Why look at a Transcriptome Catalog of all mrnas in the cell Ability to determine therapeutic targets Search space is limited to only actively transcribed areas compared to studying whole genomes Allows for the study of coding and non-coding RNAs

So if the answer may lie in RNA. How do we find it?? answer is here The answer is here Next generation sequencing

How do we study it?... Next-Generation Sequencing A new method of highthroughput sequencing What once took 10 years and millions of $$ now takes 2 weeks and $30K Can analyze all RNA in a tissue

RNA is attached to beads and placed on glass slides Beads covalently attached to slide

Data Capture Measuring all the RNA that genes are producing Michael Stratton, AACR 2009 Presentation

10 Triple Negative Breast Tumors from premenopausal women Ribosomal depleted RNA 10 Normal Breast Tissues Microdissected ductal epithelium Samples split by menstrual phase Sequence reads mapped to human genome using ABI BioScope 1.2 *Wikipedia Statistical & biological analyses using custom & commercially available software

LASER CAPTURE MICRODISSECTION before after cap For each sample: 70 frozen sections were microdissected. Four 11-hour days per sample at the University of Illinois.

Normals are quite different

Menstrual Cycle can explain some of the difference

Tumor vs. Normal 7140 Genes that are significantly different between tumor and normal!

Heterogeneity in chemo-sensitivity & outcome may be explained by fundamental differences at the gene expression level

Gene expression & SNPs as potential markers for outcome in ongoing HOG trial Gene expression as a marker of outcome PARP SNPs as a predictor of outcome for PARPi *TNBC (local) or ER+/HER2- with BRCA mutation *s/p neoadjuvant therapy with residual disease (>2cm or LN+) Primary endpoint: 2 yr DFS

Impact of having tumor vs normal comparison for therapeutic discovery Tumor vs. Tumor Tumor vs. tumor comparisons Increased likelihood of passenger findings Must sort out whether expression differences are due to: overexpression of gene in a particular tumor type OR Underexpression of tumor control Tumor vs. normal By definition ALL differences have potential to be important Schneider et al, CCR 14, 2008

The tale of 3 therapies in TNBC Treatment Target Rationale (prior data) Tumor vs Tumor Next-Gen Transcriptome Tumor vs Normal Next-Gen Fold Change/ P-value Clinical Trial Outcome Cetuximab & Gefitinib EGFR Overexpression of EGFR Not Overexpressed -1.61 (p= 0.09) NEGATIVE Imatinib c-kit Overexpression of c-kit Not Overexpressed -6.82 (p= 1.8E-06) NEGATIVE BSI-201 PARP Overexpression of PARP/Synthetic lethality in DNA repair Overexpressed 3.97 (p = 2.0E-05) POSITIVE

The $Million Question: How do we find drugs that work?

Both COBRA1 & CSNK1G2 are known inhibitors of ER-alpha (ESR1) activity

Using computers to find new therapies

Conclusions Breast cancer is more than one disease TNBC has variable chemo-sensitivity TNBC is more than one disease Targets & improved therapies are needed for TNBC

Acknowledgements Lab: Milan Radovich Bradley Hancock Nawal Kassem Abdulateef Aregbe IU Collaborators: George Sledge Susan Clare Anna Maria Storniolo Connie Rufenbarger David Flockhart Sunil Badve Lang Li Yunlong Liu Samy Meroueh