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Oncology Section RAW DRAFT Andrew Buckler (section leader), Libero Marzella, James Mountz, James Mulshine, Sonia Pearson-White, Lawrence Schwartz, Barry Siegel, Annick Van den Abbeele, Jeffrey Yap, Ricardo Avila, John Boone, Michael Graham, David Gustafson, Edward Jackson, Gary Kelloff, Paul Kinahan Vision Cancer will either be curable, or manageable as a chronic sub-acute disease, and imaging will be central to its management through the use of validated IB. Vision 2025 Socio-economic benefit Paradigm Clinical focus/relevance Performance Roadmap Socio-economic benefit (cheaper/better/faster) 1. Less expensive/time consuming development: Lower delta t and/or N for same statistical power 2. Manage cancer as chronic (personalized, sub-acute) disease Clinical care (opportunity for strategic intervention, reduction in errors, side effects, survival) 3. Pt is treated correctly for their disease. Paradigm On the day you are born, health management begins (prediction) Prevent, and treat early disease (not late) Prevention strategies well developed, i.e., avoidable, reversible, manageable Every patient that comes in the door will give a piece of themselves from which ‘omic data are derived Deal effectively with heterogeneity Early stratification of patients at risk Image is among a wide array of complementary assays that are well integrated Therapy is non-toxic and completely local Not just systemic treatments, include targeted minimally invasive surgical, ablative, brachytherapy, etc. Change patient experience, error prone, expensive… more efficient scans and diagnosis (pay for performance) Bioinformatics infrastructure robust and clinical data ubiquitous Clinical focus/relevance Imaging for least intrusive window into pre-symptomatic phase of disease Effective imaging signatures for hallmarks of pre-symptomatic disease (both resolution and sensitivity) “virtual biopsy” Complementary benefit of other biomarkers need effective data fusion approaches (incl. decision support) Genotyping->prevention (risk markers) Correlations between modality Imaging used both to stratify and to make adaptive therapy personalized to pt Tx is highly localized, image guided, no side effects Ask better questions: move full community beyond just asking whether we can detect a tumor Performance (the science of measurement as opposed to picture taking) Standardization and iterative improvement: Variance reduced: Human (e.g., protocols, compliance, structured reporting with quantitative endpoints) Sigma reduced through technology developments Calibration (incl. public data to calibrate against) (phantoms) CAD (as a way to reduce variance) Statistical framework for qualification established Multi-disciplinary approach to validation/qualification of imaging methods Device vendors (both HW and SW) market product certified against qualified Profiles Qualification data shared across vendors 510ks and biopharma NDAs (cross registration) (conformance checks established) Results easily accessible (includes unsuccessful agents, not just positive) Cancer centers should have conformance checking process, too Practice/workflow accounts for QI Methods worked out that make it easy to do (CAD) All imaging results embedded in EMR Clinical imaging = Quantitative imaging Roadmap: Year 1 Start incorporating QI in clinical trial approval process , first candidate markers used in trial designs (contributed by UPICT and QIBA) Build infrastructure in comunications: Approach to data sharing (needs to be linked to national agency initiatives) (build linkage to caBIG, etc.) (needs to be able for regulatory agencies to access and use) Establish lines of communication (incl. celebrate models of success) (incl. strategy re: publishing) Engage ASCO, ASTRO, Engage top-management of device companies and biopharma Include QI in RFAs from NIH Define regulatory approval pathway (target: February 2010 meeting) Continue IRAT (and similar) through extramural funding Roadmap: Year 3 Establish the qualification model (that is, Integrating the Imaging Biomarker Enterprise “IIBE”) (what QIBA is actually working on) First marker through qualification process (a NDA/PMA type process) (e.g., FLT, vCT) (the “predicate”) Dynamic imaging with PK/PD analysis in place (e.g., hypoxia, angiogenesis, apoptosis, metabolism) (from anatomic/structural to functional/dynamic) begun Engage CMMS Variance reduction efforts active and understood Incl. standardization of image acquisition, and processing Process of defining decision trees based on QI established and in use (structured reporting) Roadmap: Years 5-10 5 First commercial product shipped with certified marker via 510(k) (using the cross-reference) Make quantitative imaging part of every appropriate clinical trial Get payers to reimburse QI QIN up and running Structured reporting commonly used Clinicians credentialed and “pulling” Also it is in device tenders with buyers making decisions on it 10 Dynamic imaging with PK/PD analysis in common use (e.g., hypoxia, angiogenesis, apoptosis, metabolism) (from anatomic/structural to functional/dynamic) National informatics infrastructure in place to support full quantitative biomarker with meta-data Cancer 2025 Mature Emerg ent •Preclinical •Clinical trials •Screening •Clinical care •PK/PD routinely assessed with imaging commonly used •Models for translational medicine (crossspecies) more characterize d •Metabolic agents and receptor-based agents are qualified for use (e.g., VEGF) •Proliferation, apoptosis, hypoxia, …) •Inflammatory cascade characterized with invivo •Elucidated not only pathways but cellular networks (hallmarks). Define imaging based on these hallmarks, leading to go/no-go •Open access to data Multi-modality screening commonly used •Dose reduced •Lots of 5mm nodules found •Backed-up with more specific test •Characterize: •MRS, PET (more than 1 agent) •Tell btw e.g., squamous, bronchial cell, etc. •High specificity •Array of tracers that can differentiate btw oncogenic events vs. non •More widespread use of data across care cycle solutions •Localized, guided therapy •Tailored drug development •Stratification for disease based on genotype and/or mechanistic •Measures •Informatics approaches worked out to be acceptable workflow •Multi-targeted therapeutics •Signal amplification approaches for targeted for low SNR