September 20th, 2012 1:12 pm ET - W. David Dotson, Office of Public Health Genomics, Centers for Disease Control and Prevention
Michael P. Douglas, Office of Public Health Genomics, Centers for Disease Control and PreventionThe independent EGAPP working group (EWG) held its 25th meeting on September 10-11, 2012 at the CDC campus in Atlanta. Highlights included:
- Three EWG recommendation statements on the validity and utility of genetic tests are pending publication on:
- KRAS, BRAF and other markers involved in EGFR signaling, which are used to inform choice of therapies for metastatic colorectal cancer, recently submitted to Genetics in Medicine;
- Risk assessment for type 2 diabetes, in pre-submission peer-review; and
- SNP panels for prostate cancer risk assessment (based on a recently completed evidence review by investigators at the McMaster University AHRQ Evidence-based Practice Center), currently being finalized.
- Findings from evidence reviews, conducted through the AHRQ Effective Health Care Program (EHC), on PCA3 testing in the diagnosis and management of prostate cancer and CYP2C19 testing to guide antiplatelet treatment , were presented at the meeting. The EWG plans to develop corresponding recommendation statements, evaluating the validity and utility of these tests, based largely upon the findings of these reviews.
- The Knowledge Synthesis Center (KSC) will conduct systematic reviews on familial hypercholesterolemia and colorectal cancer screening – the latter topic is being done in conjunction with modeling by NCI/CISNET .
- The KSC is developing a manuscript for publication on methods and considerations for “binning findings from whole genome sequencing”.
Criticisms of evidence-based processes as requiring too much time, labor and expense are all too common. After all, a familiar argument goes, how can we expect that systematic reviews, which can take a team of trained investigators a year or more to complete, could possibly keep up with the rapidly evolving field of genomics? The experience of the EGAPP initiative has taught us that while discovery-based knowledge and resulting hype surrounding genomic applications does evolve and accumulate quite rapidly, quality information supporting the validity and utility of using these applications in health care typically does not. Nevertheless, this lopsided research environment has persisted and culminated in the impending dawn of routine clinical whole genome sequencing upon a health care system that is in large part unprepared to utilize, deal with or even understand the output. The newly published EGAPP methods update and the WGS binning manuscript in development describe different but complementary approaches designed to identify and report what is useful and actionable in the face of massive data. Neither of these EGAPP products will remediate the situation entirely, but they are productive initial steps towards collaboration with other groups and stakeholders towards a more responsive and nimble evidence-based genomics.