diagnostic solutions for antimicrobial resistance...
TRANSCRIPT
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Diagnostic solutions for antimicrobial resistance:
Identifying unmet clinical needs
Herman Goossens Laboratory of Medical Microbiology
VAXINFECTIO University of Antwerp
University Hospital Antwerp
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I identified eight (because I was only given 20 min) unmet
diagnostic needs for antimicrobial resistance and
(sometimes) will provide solutions
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We need rapid diagnostic tests to reduce antibiotic prescribing and hence the selective pressure
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• 80% of antibiotics are prescribed in primary care • Acute RTIs most common reason for GP consultation • Most infections are due to viruses • Evidence of over prescribing by GPs • Overprescribing is linked to increased antibiotic resistance
Goossens et al, 365: 579-87, Lancet 2005
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We need rapid diagnostic tests to decrease broad-spectrum toxic antibiotics and hence morbidity and mortality
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Kettetal,LancetInfectDis2011;
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Vicious circle within the HCA-pneumonia guidelines
Yu,LancetInfectDis2011;11:248-52
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We need “diagnostic-friendly” healthcare delivery systems
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‘Surgical-site S. aureus infections acquired in the hospital can be reduced by rapid screening & decolonizing of nasal carriers’ Bode L et al. NEJM 2010;362:9-17
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Bode L et al. NEJM 2010;362:9-17
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We need rapid diagnostic tests to enrich patient population in clinical trials: - to reduce costs - to develop narrow spectrum
antibiotics
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A P. aeruginosa - Focused VAP Programme
• Standard non-inferiority Phase 3 study1 – Need 336/arm or 672 evaluable patients total
• If only 10% yield P. aeruginosa, – We need 6,720 patients … for ONE trial!
Courtesy: John Rex
1Assumes 80% success rates, 10% margin, and 90% power.
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Examples of clinical trials in IMI where rapid diagnostics are needed
• Phase II RCT with anti-α-toxin staphylococcal antibody MEDI4893 for prevention of HABP/VABP (MedImmune): – Diagnostic test needed: rapid detection of S. aureus in ETA
• Phase II RCT trial with anti-pseudomonas antibodies MEDI3902 for prevention of HABP/VABP (MedImmune) – Diagnostic test needed: rapid detection of P. aeruginosa in
ETA
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S. aureus ETA Rapid Dx Weighting
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Rapid Diagnostic for POCT for P. aeruginosa colonization in endotracheal aspirates in patients on a mechanical ventilator Required diagnostic specifications: • High sensitivity (<102 cfu/mL) to identify patients as they become colonized (versus infected/pneumonia) • High specificity also desired • Validated for endotracheal aspirate samples (ETA) • Minimal hands on time (<30 min) for specimen processing • Rapid turn-around time for result (<2 hr) • Test can be run on demand without need for batching • Test can be performed outside of microbiology (ICU or step down unit) • Low cost (<$40)
• Supply up to 100 instruments to sites across Western Europe • Service and Technical support for the instruments and assay kits • Supply ~x,xxx tests between 2016 and 2020
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My lessons learned on role of diagnostics
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to aid patient enrollment in COMBACTE clinical trials with narrow-spectrum drugs (4/9 intervention trials)
Pharma: limited number of organisms in a specific sample Diagnostic companies: broad range tests
Schism between pharma and diagnostic
companies
How will test be used? What are required performance characteristics to aid patient enrolment?
Purchasing and logistical challenges Challenges to organise, track and train HCW Maintenance, Q-controls and test support Miscommunication between pharma, diagnostic company, micro lab, and CRO
Unclear exploitation How is the test developed into labeled product? Who will pay for the test?
Regulatory blind-spots Potential regulatory needs discussed too late and/or conflicting feed-back
Demand of pharma to perform test outside of
microbiology lab
Unclear function and performance
characteristics
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We need to drive reimbursement prices of rapid diagnosticstofightAMRbasedonby their medical&societalvalue
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Fast systems Alere: i Isothermal amplification: NEAR 15 min Influenza test
Handheld devices Micronics: PanNAT 1 hour 3 targets test H: 20 cm / Depth= 34.5 cm / Width: 12 cm
Tsunami of instruments
Multiple targets bioMérieux: FilmArray Reverse transcriptase Turn RNA into cDNA TAT: 1 hour
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We need to address psychological, social, and organisational barriers to support the uptake of diagnostics for antimicrobial stewardship
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GRACE Intervention Trial
• Countries: UK, Poland, Spain, the Netherlands, Belgium
• Baseline in 6,774 patients and 4,358 patients post-test
• 2x2 factorial design (Communication, CRP, Usual care)
Usual care Communication Usual care Usual care Communication training
CRP CRP training CRP + Communication training
58% 41%
31% 35%
Little et al, Lancet 2013
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Figure 2. Mean (SD) CRP concentration by microbiological diagnosis for LRTI subjects with (n=141) and without CAP (n=2963).
Mean (SD) CRP concentration by microbiological diagnosis for LRTI subjects with (n=141) and without CAP (n=2963)
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Confidential; manuscript in preparation
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Long road to successful uptake of diagnostics
• Rapid and cheap test available • Demonstrated benefit in reducing antibiotic
prescribing in a multinational, cluster, randomized, factorial, controlled trial (published in The Lancet)
• Supported by microbiological and cost-effectiveness research
• Reimbursed in the Netherlands • Yet not used in primary care
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We need different business models to support uptake of new, innovative, and expensive diagnostics
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NEXT GENERATION SEQUENCING
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Epidemiology and Phylogeny of an Outbreak of MRSA Sequence Type 2371 at a Baby Unit
HarrisLID2013;13:130-36
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Value-based procurement of IVDs to address AMR • Currentapproachtoprocurementbasedonprice-basedpurchasesreducesinnovation,discouragestheadoptionofnewtechnologies,makesthemarketunattractiveforSMEs
• NewEUdirectiveonpublicprocurementinFebruary2014– Moveawayfromup-frontprice-onlypurchasecosts– Factorsinoutcome,quality,totalcostsacrosstheproductlifecycleandbroadersocio-economiccriteria
• ItwouldencourageIVDcompaniestoinvestininnovation– Minimumvolumeassurances– Enablingthemarkettorespondtoserviceneeds
• ShouldbebasedonHTA(nextslides)• Couldincentiviseclinicalvalueofdiagnostics• Shouldaccelerateregulatoryapproval• ShouldfacilitatebetterreimbursementofIVDtestsaddressingAMR• Shouldbeaccompaniedwithmeasurestoaddresssocial,psychological,organizationalbarriers
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HTA Reports by medical technology type
2014 2015 2016
TotalHTAreports 372 372 304
MedicalDevices(kneereplacement,spinalcordstimulation,silverdressing) 289 293 223
IVDs(e.g.serumbiomarkers,genetictesting,screeningforhumanpapillomavirus) 28 16 40
Imaging(e.g.PET/CT,MRI,Echocardiography) 29 25 22
Others(e.g.spermwashing,ReCellSpray-OnSkin,sterilewaterinjections,) 26 38 19
MedicalDevices78%
Imaging8%
IVDs7%
Other7%
2014
MedicalDevices79%
Imaging7%
IVDs4%
Other10%
2015
StatisticbasedonSynergusdatabase(link)*EU28+Switzerland+Norway
MedicalDevices74%
IVDs13%
Imaging7%
Other6%
ChartTitle
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HTA for IVD (of ID / AMR) • HTAofIVDsrepresented8%ofallHTAin2014-2016;HTAofnewIVDsinlessthan1%(Synergusdatabase)
• HTAforIVD/ID/AMRareverycomplex(screening,diagnosis,treatment,prognosis,monitoring)
• HTAdatarequirements/acceptanceasevidence,andtimepointsduringlifecycle,notalignedbetweencountriesandevenwithincountries
• ResponsibilityanddecisionpowervariesbetweenHTAagencies• HTAarerarelyusedtoinformdecisionatnational,regional,hospitallevel,communitylevelonaccess,reimbursement,use,valueofIVD
• Need“fit-for-purpose”pragmatic,streamlined,standardHTAofIVDsaddressingAMR
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• Prepare public procurement of innovative rapid diagnostics for tailoring antimicrobial treatment
• Deadline 18 April 2018
• Build NGS platform for use of NGS tests in routine diagnostics for personalized medicine
• Deadline 16 April 2019
• Build fit-for-purpose HTA models • Focus on personalized medicine and companion diagnostics • Deadline 18 April 2018
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We need Clinical Trial Networks to demonstrate the clinical evidence of diagnostics
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• Per Performance Plan
• PP to address Clinical Evidence, consisting of:
– Scientific Validity: Literature Search Documented
– Analytical Performance: Per applicable Requirements
– Clinical Performance: Per clinical study, if necessary; Population
effects
• Performance Report updated continuously throughout lifecycle
New IVD Regulation: Areas of Greatest Impact: Performance Evaluation
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Slovenia: 3 hospitals; 3 laboratories
Albania: 8 hospitals; 9 laboratoriesAustria: 11 hospitals; 6 laboratories
Belarus: 1 hospital; 2 laboratoriesBelgium: 22 hospitals; 17 laboratories
Bosnia and Herz.: 7 hospitals; 5 laboratoriesBulgaria: 15 hospitals; 14 laboratories
Croatia: 15 hospitals; 10 laboratories
Cyprus: 1 hospitals; 1 laboratory
Czech Republic: 25 hospitals; 20 laboratoriesDenmark: 8 hospitals; 6 laboratories
Estonia: 5 hospitals; 2 laboratories
Finland: 9 hospitals; 1 laboratory
France: 93 hospitals; 56 laboratories
Georgia: 1 hospital
Germany: 53 hospitals; 54 laboratories
Greece: 44 hospitals; 36 laboratories
Iceland: 1 hospital; 1 laboratoryIreland: 10 hospitals; 4 laboratories
Israel: 20 hospitals; 15 laboratoriesItaly: 53 hospitals 27 laboratories
Italy: 53 hospitals; 27 laboratories
Kosovo: 4 hospitals; 5 laboratoriesLatvia: 6 hospitals; 3 laboratories
Lithuania: 1 hospital; 2 laboratories
Luxembourg: 1 hospital; 1 laboratory
FYROM: 5 hospitals; 20 laboratories
Moldova: 6 hospitals; 2 laboratories
Montenegro: 8 hospitals; 10 laboratories
Netherlands: 34 hospitals; 26 laboratories
Norway: 3 hospitals; 2 laboratories
Poland: 22 hospitals; 5 laboratories
Portugal: 30 hospitals; 14 laboratories
Spain: 68 hospitals; 59 laboratories
Romania: 29 hospitals; 20 laboratories
Serbia: 30 hospitals; 26 laboratories
Slovakia: 10 hospitals; 5 laboratories
Sweden: 10 hospitals; 3 laboratoriesSwitzerland: 11 hospitals; 4 laboratories
Turkey: 52 hospitals; 48 laboratoriesUkraine: 1 hospital
United Kingdom: 93 hospitals; 29 laboratories
IMI- COMBACTE network infrastructure (March 2017)
hospitals 827
laboratories 583
countries 42
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COMBACTE Clinical studies
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January 2018: 8070 patients enrolled
Studyname Sponsor Patients Type Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Q4ASPIRE-ICU UMCU ICU_VAP EpiSAATELLITE AZ/MI ICU RCTASPIRE-SSI UMCU Various EpiWP6Etbd AZ/MI ICU RCTANTICIPATE DaV Various EpiWP8D MedComp ICU RCT /210
EURECA SAS Various EpiREJUVENATE Pfizer ICU+ RCTREVISIT Pfizer ICU+ RCT /300
EVADE AZ/MI ICU_VAP RCT WP4B AZ/MI ICU_VAP RCT /980RESCUING ICS-HUB cUTI Epi 1013(recruitmentcompleted)WP6G AiCuris cUTI RCT /240WP6H AiCuris cIAI RCT /225
COMBACTE WP1 UnivLeeds Epi /tbcCDI WP2 UnivLeeds /tbc
MERMAIDS UOx ARBO Epi MERMAIDS UOx ARI Epi REMAP-CAP UMCU ICU adaptRCT
Shionogi CREDIBLE-CR Shionogi RCT 20/150MK-7655A RESTORE-IMI2 Merck ICU RCT 230/536HABP/VABP CTTI HAP/VAP Epi 1006/1000Colistin OVERCOME NIH ICU RCT 157/444(outsideofEurope)
preparationphase trialperiod 8070
70/285
425/1500746/20007/4000
40/40
20182014 2015 2016 2017
205/2851341/2000
580/5000
1019/1000
1368/2000
2019
PREPARE
COMBACTENET
COMBACTEMAGNET
COMBACTECARE
recruitment completed
recruitment completed
recruitment completed
recruitment completed
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Time for a Paradigm Shift of Infectious Diseases Clinical Research
Expensive
Inefficient
Rigid design
One-off initiatives
Alienated patients
Irregular
Efficient
Coordinated and sustainable
Patient-centered
Participatory and precision medicine
Responsive and adaptive
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Detailed Design of Business plan and operating model
Construct & Implement
2016
High level Design
High Level design completed
end of current funding PREPARE
end of current funding COMBACTE-Net
2022 2017 2018 2019 2020 2021
FUNDING THROUGH IMI2 FOR Dx PART (VALUE-Dx – 28.2.2018)
FUNDING FOR ID STUDIES TO BE ACQUIRED FROM PUBLIC AND PRIVATE SECTOR
FUNDING THROUGH H2020 (CSA call – 18.4.2018)
ECRAID: Our plan and timelines
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• Develop business plan to ensure sustainability of a clinical trial network • Build on PREPATE and COMBACTE • Deadline 18 April 2018
• Develop a business plan for CTN on diagnostics • Demonstrate the clinical and societal value of rapid diagnostics for AMR • Build around CA-ART • Deadline 28 February 2018
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Unique opportunities for pharma, academia, the EU and its citizens
• Incentiveforpharmatoinvestinantibioticdiscovery• Allowstobroadenthespectrumtootherantimicrobialdrugs,vaccines,anddiagnostictests
• Allowsinvestigatordriventrials• Allowsnewmodelsofclinicaltrials(e.g.AdaptivePlatformTrials)
• Createsinnovationofthepublicandprivate(e.g.SMEs)sector
• Allowsrapidclinicalresearchresponseintheeventofapandemicthreat
• Resultsinimprovingqualityofcaredeliverytoourpatients
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Many thanks!