Dr Yvonne Wallis Consultant Clinical Scientist West ......Cancer Biomarkers Cancer is a genetic...
Transcript of Dr Yvonne Wallis Consultant Clinical Scientist West ......Cancer Biomarkers Cancer is a genetic...
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Dr Yvonne WallisConsultant Clinical Scientist
West Midlands Regional Genetics Laboratory
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Personalised Therapy/Precision Medicine Selection of a therapeutic drug based on the presence or absence
of a specific drug target (biomarker) in the tumour that renders the tumour cells sensitive or resistant to therapy
Diagnosis TreatmentPrognosis Monitoring
Cancer Clinical Pathway
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Benefits of Personalised Therapy PATIENTS/CLINCIANS
Access to more effective targeted treatments Fewer adverse events
SCIENTISTS/CLINICIANS Biomarker knowledge - improved drug development More efficient clinical trial design
NHS Right patient, right drug, right time Time and cost savings
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Cancer Biomarkers
Cancer is a genetic disease Acquired changes in oncogenes and tumour suppressor genes Control cell division, DNA repair, angiogenesis, cell death Driver mutations - oncogenesis
“Same site” tumours Variation in genetic make-up Different responses to treatment
Personalised cancer care Tumour classification based on genetic make-up rather than
tumour site Management based on specific genetic biomarkers
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Early examples of Personalised Therapy
Breast cancer ERBB2 oncogene expression Amplification 35% breast tumours/Poor prognosis Herceptin (first solid tumour monoclonal antibody)
Non small cell lung cancer EGFR mutation status assessed Anti-EGFR tyrosine kinase inhibitors
Sensitising mutations (exons 19 and 21) Resistance mutations (exons 18 and 20)
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Genetic Biomarkers – Somatic variants
Analysis of tumour DNA FFPE – formalin fixed paraffin embedded tissue FF – Fresh frozen ctDNA – circulating tumour DNA
Genetic testing technologies
Single Target Tests Multiple Target Test
Pyrosequencing Next Generation Sequencing
ddPCR
Sanger sequencing
FISH
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Challenges - Heterogeneity
Tumour heterogeneity Inter- and intratumour genetic
subclones Multi-region sampling
Primary vs metastasis Circulating tumour DNA
Cell free tumour-derived DNA in plasma
Reflects whole tumour genome Levels reflect tumour burden
Tissue heterogeneity Normal and tumour cell types Background wild type DNA “Mask” tumour mutations Macrodissection to enrich for
tumour
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Challenges - FFPE Formalin Fixed Paraffin Embedded tissue
Most widely practiced method for clinical sample preservation Formalin preserves the cytoskeletal and protein structure of the cells Allows the cells to be stained and abnormalities to be detected FFPE workflows embedded in clinical pathways for cancer diagnosis
Possible to extract DNA/RNA from these tissues Enabling molecular profiling Poor quality templates
Nucleic acids are highly fragmented Presence of contaminates Non-reproducible cytosine deamination artefacts occurs
in one strand only
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Challenges - FFPE DNA QCQuantity• dsDNA• Fluorometry – Qubit/Picogreen
Quality• Fragmentation – Bioanalyzer, tapestation• “Amplifiability” - qPCR
Contaminants• UV absorbance – Nanodrop• qPCR
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Challenges – Genetic complexity
Wide spectrum of somatic variation
SNVs, indels, CNVs, structural variants, “mutational signatures”
Multiple changes important to detect for effective personalised therapy
Multiple technologies used
Circos plot generated from whole genome sequencingGenome wide visualisation of somatic variation
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Challenges - Interpretation
Standardisation of interpretation & reporting Four tiered system to categorise somatic variants Based on impact on clinical care –
Predicts sensitivity/resistance to therapy https://www.mycancergenome.org/ Supports inclusion in a clinical trial https://clinicaltrials.gov/ct2/home Influences prognosis, assists diagnosis Warrants surveillance measures for early detection
Classification Tier I: Strong clinical significance Tier II: Potential clinical significance Tier III: Unknown clinical significance Tier IV: Benign/likely benign
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Next Generation Sequencing –Emerging technology in personalised medicine
Advantages Massively parallel sequencing – multiple targets simultaneously Sensitivity (<1%) – high read depth potential Broad spectrum of mutations Difficult template tolerant Low cost per base High throughput
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Basic Steps of NGS: DNA to Data
Sequencing• Application
dependent• Single read• Paired-end analysis• Mate-pair analysis• Produces “reads”
Bioinformatics• Base calling• Alignment• Variant calling• SNVs• CNVs• SVs
Further Bioinformatics• Annotation• Variant Interpretation• Assess pathogenicity
Specimen• Germline• Blood• Saliva/other tissue
• Somatic• Tumour• Fresh Frozen/FFPE
Nucleic acid extraction• DNA • RNA• Template dependent• Automation options
Library preparation• “Target enrichment “• Gene Panel• Whole Exome• Whole Genome
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NGS strategies Strategy: Panel Test Whole Exome Whole GenomeTarget: SELECTED genes All CODING genes WHOLE DNA sequence
Size: 10-500 genesVariable size
~20,000 genes 30 million bases
Whole genome 3000 million bases
Coverage: >99% target coverage
>98% coverage >95% coverage
Depth/Sensitivity: +++ ++ +
Throughput: +++ ++ +
Data storage: + ++ +++
Cost: £ ££ £££
Variants: Gene related variants
30,ooo variants 3 million variants
Interpretation: Actionable mutations
Novel variantsIncidental findings
Novel variantsIncidental findings
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Sensitivity of NGS –Confidence for low level variant detection
Tumour %
% of mutant reads if variant at 10% level
Ratio of mutant reads
Sequencing depth required to obtain 10 mutant reads
5% 0.5% 1/200 2000
10% 1% 1/100 1000
20% 2% 1/50 500
40% 4% 1/25 250
50% 5% 1/20 200
100% 10% 1/10 100
0
500
1000
1500
2000
2500
5 10 20 40 50 100
Rea
d de
pth
Tumour %
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CR-UK Stratified Medicine Programme• CR-UK the world's largest independent cancer research charity
• SMP is their hope to make personalised medicine standard practice of care for all cancer patients
• Launched in 2010
Our vision is to establish a national molecular diagnostics service delivering high quality, cost effective tests for patients, with routine consent for the collection, storage and research use of genetic, treatment and outcomes data.
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Phase 1 (SMP1)
• Sep 2011 – Aug 2013• 9000 patients• Breast, colorectal,
lung, melanoma, ovarian, prostate
• 8 Clinical Hubs• 3 Technical Hubs• Proof of principle• NGS panel vs
single tests
Phase 2 (SMP2)
• Sep 2013 >• 2000 patients• Lung (NSCLC)• 18 Clinical Hubs• 3 Technical Hubs• 28 gene panel• Linked to National
Lung Matrix Trial
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Stratified Medicine Programme
Cardiff
Cardiff
University Hospital of
Wales
Morriston
Singleton
Royal Gwent
Velindre
Manchester
The Christie
Wythenshawe
SalfordRoyal
Pennine Acute
Glasgow
Royal Infirmary
Western Infirmary
Southern General
Golden Jubilee
Gartnavel
Victoria Infirmary
Stobhill Hospital
Birmingham
Birmingham
University Hospital
City
Edinburgh
Western General
Royal Infirmary
Cambridge
Addenbrooke's
Papworth
RMH
RMH
Marsden
Royal Brompton
Leeds
St. James's
General Infirmary
Technology HubsClinical HubsFeeder Hospitals
Infrastructure versus population density
The SMP1 Network: 3 Technology Hubs, 8 Clinical Hubs, 26 Feeder Hospitals
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SMP2 Structure
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SMP2 NGS Test– Panel linked to Matrix Trial– Detects a range of variations across 28 genes– Multiple changes in the same patient– For trial eligibility the wild type status of
some genes is critical– The above 2 pieces of information are key to
determine Matrix trial arm eligibility
CR-UK NGS Panel 2
Nextera hybridisation 28 genes
Detects SNVs, indels, CNV, SV
Matched blood sample to subtract germline
variants
AKT1 ALK BRAF CCND1
CCND2 CCND3 CCNE1 CDK2
CDK4 CDKN2A EGFR FGFR2
FGFR3 Her2* HRAS KRAS
MET NF1 NRAS NTRK1
PIK3CA PTEN RB1 RET
ROS1 STK11 TSC1 TSC2
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National Lung Matrix Trial Series of single arm phase II trial arms Testing experimental targeted drugs Population stratified by pre-specified putative actionable
biomarkers Bayesian adaptive umbrella design Arm for population with no actionable genetic changes
8 investigational medicinal products 21 patient cohorts
NSCLC histology Molecular status
https://www.birmingham.ac.uk/research/activity/mds/trials/crctu/trials/lung-matrix/professionals/index.aspx
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Treatment arms – wild type IMPORTANTArm Medicinal
ProductCohort NSCLC
HistologyMolecular Status
C Palbociclib –CDK-4/6 Inhibitor
C1 SCC CDKN2A loss +Wild type RB
C2 ADD or NOSNSCLC
CDKN2A loss +Wild type RB
C3 NSCLC CDK4 amplification +Wild type RB
C4 NSCLC CCND1 amplification +Wild type RB
C5 NSCLC STK11 or TSC1/2 mutation +KRAS/NRAS/NF1 mutation +Wild type RB
C6 NSCLC KRAS mutation +Wild type RB, STK11, PIK3CA, PTEN, AKT, EGFR, FGFR2/3, TSC1/2, HER2
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Genomics England - 100KGP Transformation of NHS
WGS can become a routine clinical investigation Aim to sequence 40,000 genomes from 20,000 cancer patients Paired blood and tumour
Variant subtraction Clinical interpretation
Enables genome wide inspection of somatic variants Mutation signatures
Tumour mutation burden Indicator for Immunotherapy
Tumour heterogeneity Multi-region sampling
Pertinent germline findings – reporting back
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Actionable gene-based classification toward precision medicine in gastric cancer Ichikawa et al, Genome Medicine (2017) 9:93
Poor outcome for unresectable and recurrent cancers Intertumour heterogeneity significant hurdle to identifying optimised
targeted therapies in GC Current molecular classifications not associated with targeted therapies
Comprehensive genomic profiling in 207 gastric tumours
435 cancer genes69 FDA “actionable” genes
EBV infection &Microsatellite instability status
141/207 tumours (68%) = actionable gene alteration
N = 32Hypermutated
N = 25ERBB2
N = 10CDKN2A/B
N = 10KRAS
N = 9BRCA2
N = 12ATM
N = 109Minor/No alterations
Novel Classification
Each associated with an FDA approved targeted therapy (clinical trials needed to show effectiveness)
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References