Congressional Action Needed To Optimize Regulation Of Genomic Tests

Researchers from University of Houston and University of Washington Co-author Special Report in New England Journal of Medicine

May 27, 2015, 12:46 ET from University of Houston Law Center

HOUSTON and SEATTLE, May 27, 2015 /PRNewswire-USNewswire/ -- The latest generation of genomic testing offers a chance for significant improvements in patient care, disease prevention, and possibly even the cost-effectiveness of healthcare, but Congress needs to act to incentivize the development of the massive data systems that doctors and regulators will need in order to make these tests safe and effective for patients.

A team of three leading researchers in law, bioethics, and medical genetics believes the solution lies in bolstering existing regulatory oversight with a systematic, ongoing program of postmarket data collection to continue studying tests after they are in use and resolve lingering questions about the health impact of as-yet-poorly-understood genetic variants.

The Special Report by Barbara J. Evans, Ph.D., J.D. of the University of Houston Law Center, and Wylie Burke, M.D., Ph.D. and Gail P. Jarvik, M.D., Ph.D, both of the University of Washington School of Medicine, appears ahead of print in the May 27 on-line edition of New England Journal of Medicine, the leading U.S. journal of original medical research and commentary.

The authors note that modern, genomic-scale tests can generate large numbers of data points for each tested patient, including numerous genetic variants—changes from the expected DNA sequence of an "average" genome. A genetic variant is said to have clinical validity if its impact on human health is well understood, so that detecting the variant supplies useful information about the patient's health or predispositions to disease. One limit to genomic testing is that the science is still in an early stage of development and the clinical significance of most of the variants these tests detect is not yet known. Dr. Jarvik notes that this "creates a risk that patients will base important medical decisions on diagnoses or predictions that later prove incomplete." For example, a genetic variant that has unknown significance at the time of the test may instead confer a high risk of breast cancer. 

The U.S. Food and Drug Administration (FDA) has been grappling with how to regulate these tests and recently proposed to assess their safety and effectiveness by reviewing whether the test accurately detects a person's variants and whether the results have clinical validity. The FDA has suggested it might base its decisions about clinical validity on high-quality external genetic databases, such as those curated by the National Institutes of Health (NIH) ClinGen program and deposited in its ClinVar database and other FDA-recognized external databases.   

Evans, Burke, and Jarvik argue the genomic data resources that will be necessary to assure patients the maximal benefits of genomic testing do not now exist and will have to be built. "Whole-genome sequencing detects more than 3.5 million variants in a typical person, including 500,000 that are rare or novel. ClinVar, while it is an excellent data resource, currently only has about 77,000 unique genetic variants in it, and many of these are variants of unknown clinical significance," notes Dr. Burke. The President's recent Precision Medicine Initiative proposes to develop a database reflecting genetic and clinical data for one million volunteers, but even this will not be large enough.  Figuring out the clinical impact of a novel gene variant can require data for tens or even hundreds of millions of people.

The researchers' Special Report explores what it will take to develop the needed data resources and recommend an approach—ongoing postmarketing surveillance--that the FDA successfully implemented to improve the safety of approved drugs after a series of serious safety incidents, including those with rofecoxib (Vioxx) during the last decade.  This approach would involve collecting data not just from research settings, as the ClinVar system was originally designed to do, but also from commercial clinical laboratories that administer genomic tests to large, diverse patient populations. Unfortunately, the FDA's current medical device regulations—which date back almost 40 years—do not give the agency all the legal powers it would need to implement such a solution. Congress would need to authorize the development of new genomic data systems, as Congress did in 2007 for drugs. 

The authors acknowledge that the needed genomic data systems will require significant investments that go beyond what federal funding agencies like the NIH can or should support. "The United States has a long history, dating back 150 years, of incentivizing private investors to help build our major national infrastructures like the electric power grid and telecommunications network. We as a nation know how to do this," Dr. Evans notes.  Developing nationally scaled genomic data systems for patient safety, public health, and scientific advancement, they believe, is our nation's next big infrastructure challenge. The authors call for legislative reforms to enable public-private partnerships and direct private investment and to enhance appropriate access to the crucial data resources, subject to careful regulatory oversight to protect genetic privacy and engender public trust.    

This work was funded by NIH (grants U01HG006507 and U01HG007307).

About the University of Houston
The University of Houston is a Carnegie-designated Tier One public research university recognized by The Princeton Review as one of the nation's best colleges for undergraduate education. UH serves the globally competitive Houston and Gulf Coast Region by providing world-class faculty, experiential learning and strategic industry partnerships. Located in the nation's fourth-largest city, UH serves more than 40,700 students in the most ethnically and culturally diverse region in the country.

About the University of Houston Law Center
The University of Houston Law Center is the leading law school in the nation's fourth-largest city. Founded in 1947, it is a top-tier institution awarding Doctor of Jurisprudence (J.D.) and Master of Laws (LL.M.) degrees. The Law Center is fully accredited by the American Bar Association and is a member of the Association of American Law Schools.

About the UW Medicine
UW Medicine's mission is to improve the health of the public by advancing medical knowledge, providing patient care, and training the next generation of health professionals.  It is noted for leadership in conducting biomedical research and   in ameliorating health-care disparities for ruraland other medically underserved populations.   Its clinical system includes Harborview Medical Center, Northwest Hospital & Medical Center, Valley Medical Center, UW Medical Center, UW Neighborhood Clinics, UW Physicians, UW School of Medicine and Airlift Northwest.
Visit http://uwmedicine.org for details. Twitter: @UWMedicineNews

Media Contacts: Carrie Criado, 832/576-6207, cacriado@uh.edu
Leila Gray, 206/685-0381, leilag@uw.edu

Logo - http://photos.prnewswire.com/prnh/20150327/195030LOGO

 

SOURCE University of Houston Law Center



RELATED LINKS

http://www.law.uh.edu/