Newsroom

December 16, 2019

Ambry Genetics Receives New York State Approval to Offer Paired RNA and DNA Genetic Testing for Hereditary Cancer Risk

+RNAinsight is now available for New York patients, and will help identify thousands more patients at increased risk for cancer

(Aliso Viejo, CA) December 16, 2019: Ambry Genetics® (Ambry), a leading clinical genetic testing company, announced today that the New York State Clinical Laboratory Evaluation Program (CLEP) has approved Ambry’s next-generation, paired RNA and DNA genetic test for hereditary cancer risk. +RNAinsight enables clinicians – for the first time ever – to conduct both DNA and RNA genetic testing at the same time. This is the first genetic testing advancement in over a decade to significantly increase the diagnostic yield (meaning the number of patients identified with a specific hereditary risk for cancer) in genes like BRCA1 and BRCA2. With +RNAinsight, Ambry is the first and only lab to offer paired RNA and DNA genetic testing for hereditary cancer risk.

The New York State Department of Health established CLEP to ensure test accuracy and reliability for the state’s residents through strict evaluation standards. With CLEP approval, Ambry’s +RNAinsight is now available to patients in New York and in all 50 states.

“With +RNAinsight, New Yorkers can now receive the most accurate and comprehensive determination of whether they have genetic mutations that increase their risks for breast, colon, and other hereditary cancers,” said Aaron Elliott, PhD, CEO of Ambry Genetics. “New York conducts the most rigorous state reviews of lab-developed tests, and its approval further validates +RNAinsight as a new clinical standard for hereditary cancer testing.” 

DNA testing alone – the previous clinical standard to determine hereditary cancer risk – may provide an inconclusive result on whether a genetic variant (an error in our DNA) increases cancer risk. Moreover, standard DNA testing excludes large portions of DNA, and therefore can miss disease-causing mutations and inaccurately provide a negative result. Adding +RNAinsight (RNA added to the current DNA test) overcomes these limitations for a significant number of patients and provides more evidence than DNA alone about whether the genes in our DNA have mutations. Clinicians can now use this information from +RNAinsight with patients and their relatives to try to detect cancer early and to prevent cancer from developing.

ABOUT +RNAInsight™

+RNAinsight™, paired with Ambry Genetics’ hereditary cancer DNA tests, uses next-generation sequencing to concurrently analyze a patient’s DNA and RNA, another layer of genetic information. +RNAinsight identifies more patients who have mutations that increase their cancer risks than through standard DNA-only testing by overcoming limitations of DNA testing. +RNAinsight enables more accurate identification of patients with increased genetic risks for cancer, finds actionable results that may otherwise be missed, and decreases the frequency of inconclusive results. +RNAinsight is now available through doctors and genetic counselors around the country. For more information on +RNAinsight, please go to ambrygen.com/RNAinsight

About Konica Minolta Precision Medicine

Konica Minolta Precision Medicine, Inc. (“KMPM”) based in Aliso Viejo, CA is a subsidiary of Konica Minolta, Inc. that includes Ambry Genetics Corporation and Invicro LLC. Founded in 2018 on the belief that groundbreaking medical breakthroughs are possible by concentrating efforts on the health expression map, the undiscovered territory between an individual’s genetics and biological impacts, and quantifiably measuring health over time. KMPM’s health intelligence and visualization platform brings together the most novel and diverse set of data from genes, proteins, cells and tissues with sophisticated analytics and world-leading scientific and medical expertise, enabling more prescriptive, proactive and preventive care. For further information, visit: KonicaMinoltaPrecisionMedicine.com

Press Contact:
Liz Squire
press@ambrygen.com
(202) 617-4662