IMMUNOSELECT-R⢠IDENTIFY AND PRIORITIZE CANDIDATE
Transcription
IMMUNOSELECT-R⢠IDENTIFY AND PRIORITIZE CANDIDATE
IMMUNOSELECT-R™ IDENTIFY AND PRIORITIZE CANDIDATE NEOANTIGENS FROM CANCER EXOME SEQUENCING RESULTS WITH UNMATCHED ACCURACY WHAT IS IMMUNOSELECT -R™? Neoantigens are a class of immunogens based on the personal, exquisitely tumor-specific mutations found uniquely in each patient’s tumor. Combining PGDx’s highly accurate cancer exome analyses (CancerXome™ ) with in silico neoantigen prediction, ImmunoSelect-R™ identifies and prioritizes the most relevant mutation-derived neoantigens to enable adoptive T-cell transfer, cancer vaccine development, and prediction of clinical utility of checkpoint inhibitors. CANCER-IMMUNITY CYCLE 4 Priming and activation (APCs & T cells) 3 CHECKPOINT INHIBITOR (e.g. ANTI-CTLA-4) blood vessel lymph node 5 Infiltration of T cells into tumors (CTLs, endothelial cells) 6 Recognition of cancer cells by T cells (CTLs, cancer cells) NEOANTIGEN ID Cancer antigen presentation (dendritic cells/APCs) IMMUNOSELECT-R™ DELIVERABLES Trafficking of T cells to tumors (CTLs) •Unparalleled cancer exome sequencing accuracy to ensure identification of true somatic mutations — 95% sensitivity and 97% PPV down to 10% mutant allele frequency at 150x coverage • Accurate HLA typing using whole exome sequencing •Prediction and prioritization of the most relevant neoantigens from exome-based mutations and novel open-reading-frames 2 TUMOR ADOPTIVE T CELL THERAPIES VACCINES Release of cancer cell antigens (cancer cell death) 7 1 Killing of cancer cells (Immune and cancer cells) CHECKPOINT INHIBITOR (e.g. ANTI-PD-1) SOURCE: “Oncology meets immunology: the cancer-immunity cycle”, Immunity, 25 July 2013 IMMUNOSELECT-R™ PIPELINE WT/Somatic Peptides (Mutation, neoORF) HLA-information 1_BRAF ISQFWYDSY [F/T] SVPAFWQDY 1_HAUS3 SERFWVEYYS [CFTF/HSVP] WFSYRV Generate Fasta of WT/Som Peptide Pairs (8-11aa) Expression (mRNA or Protein) Similarity to Known Ag MHC Binding Affinity * .fastq HLA-A01: 01 HLA-A26: 01 In Silico HLA-typing HLA-A01: 01 HLA-A26: 01 Mutant Allele Frequency Self-Similarity Antigen Processing Candidate Neo-Ag (MHC-peptide IC50< 500nM) Prioritized Neo-Ag for Experimental Follow-up EXAMPLE REPORT OUTPUT Patient ID HLA Type Gene Name Peptide ID MUT Peptide MUT MHC Affinity MUT CTL Class Mean Exp in Tumors Priority Patient 1 HLA-A*02:01 GAS7 1_p09490_10 SLADEAEVYL 14.4 E 236 High Patient 1 HLA-B*44:03 CSNK1A1 59_p06000_8 GLFGDIYL 5.72 E 4633 High Patient 1 HLA-A*24:02 KIAA031 124_p11981_11 KLLQQLNGWYM 25.3 E 2063 High Patient 1 HLA-A*02:01 RRP1B 197_p19240_11 FLPKPLFFFRA 16.63 E 1111 High PERSONAL GENOME DIAGNOSTICS | 2809 BOSTON STREET, SUITE 503 | BALTIMORE, MARYLAND 21224 | TEL (888) 571-2163 IMMUNOSELECT-R™ IS FOR RESEARCH USE ONLY, NOT FOR DIAGNOSTIC PURPOSES. PERSONAL GENOME DIAGNOSTICS IMMUNOSELECT-R™ OVERVIEW ONLY CANCERXOME ™ DELIVERS THE SENSITIVITY AND SPECIFICITY REQUIRED TO PREVENT FALSE POSITIVE MUTATIONS FROM CONFOUNDING NEOANTIGEN IDENTIFICATION NUMBER OF DNA BASE PAIRS VALIDATED WITH AN INDEPENDENT METHOD USED FOR PIPELINE OPTIMIZATION Using 100 to 1,000 times more independently validated data points to optimize the bioinformatics pipeline ensures unmatched accuracy of PGDx exome sequencing. IMPACT OF INCREASED SPECIFICITY ON EXOME SEQUENCING PPV Pipelines that have not been validated against whole exome Sanger sequencing using matched normal controls will be less than 99.99999% specific. 97% 100% SMALL COMMERCIAL LABS HOSPITAL LABS <1 Million Mass spectrometry 100,000 Sanger sequencing of hot spots in key genes <1,000 Targeted arrays 80% PGDx CancerXome™ can reduce false positive somatic mutation calls by 50% to 90% over competitor exome tests. 74% PGDx PERFORMANCE FOUNDATION MEDICINE 90% Positive Predictive Value (Polymorphism is a True Somatic Variant) PGDx Hundreds of millions of DNA base pairs using whole exome Sanger sequencing 70% 60% 50% COMPETITOR PERFORMANCE 40% 30% 22% 20% 3% 10% 0.3% 0% 99.9% IMMUNOSELECT-R™ VALIDATION 99.99% 99.999% 99.9999% 99.99999% IMMUNOSELECT-R™ CONSISTENTLY RANKED EXPERIMENTALLY VALIDATED NEOANTIGENS WITHIN TOP 20% OF ALL NEOANTIGEN CANDIDATES DERIVED FROM WHOLE EXOME SEQUENCING •Identified 18 out of 19 experimentally validated neoantigens as being strong neoantigen candidates, suggesting an assay sensitivity of greater than 90% Sample #Mutations #Neo-Ag (IC50<500nM) #Neo-Ag Post Prioritization Rank of Validated Neo-Ag Patient 1 504 128 55 1, 14, 15, 16 SOURCE OF DATA: cancerimmunity.org/peptide/mutations/ Patient 2 257 277 30 1, 2, 3, 4, 15, 16 Patient 3 58 97 30 9, 10, 14, 15, 16 •Reproduced the tetra-peptide signature predictive of clinical benefit of CTLA-4 blockade in melanoma SOURCE OF DATA: “Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma” New England Journal of Medicine, 04 December 2014 SOURCE OF DATA: “Mining exomic sequencing data to identify mutated antigens recognized by adoptively transferred tumor-reactive T cells” Nature Medicine, 05 May 2013 IMMUNOSELECT-R™ KEY PERFORMANCE ATTRIBUTES •Unparalleled cancer exome sequencing accuracy to ensure research is focused on true somatic mutations for neoantigen prediction — 95% sensitivity and 97% positive predictive value down to 10% mutant allele frequency at 150x coverage • Works on FFPE or frozen tissue •Matched patient normal (germline DNA) is required for optimal results •Accurate inference of HLA typing from whole-exome sequencing •Neoantigen analysis can be offered alone or in combination with CancerXome™ and completed within 48 hours of tumor mutation analysis completion •Effective in silico pipeline to discover and prioritize candidate neoantigens by incorporating the following: —Comprehensive Identification of tumor-specific mutated peptides and neo-ORF —State-of-the-art prediction of HLA-types, antigen processing and MHC-peptide binding —Proprietary strategy to select most-relevant candidate neoantigens for experimental validation IMMUNOSELECT-R™ IS FOR RESEARCH USE ONLY, NOT FOR DIAGNOSTIC PURPOSES. INNOVATIVE GENOMIC TECHNOLOGIES TO SOLVE FUNDAMENTAL CHALLENGES IN ONCOLOGY LEARN MORE AT PERSONALGENOME.COM OR CALL FOR A QUOTE 443.602.8833