简体中文 | 繁體中文 | English

Pathway genomics

Pathway Genomics Launches BreastTrue NGS High Risk Breast Cancer Panel with PALB2

2014-09-11 17:14
  • zh_cn
  • zh_hant
  • en

SAN DIEGO--()--Pathway Genomics Corporation, a San Diego-based CLIA and CAP accredited clinical laboratory that offers genetic testing services globally, today announced it has launched BreastTrueTM High Risk Panel, a blood or saliva next-generation sequencing test with deletion/duplication analysis to detect mutations in seven high-risk breast cancer susceptibility genes, including BRCA1, BRCA2 and PALB2.

Recent studies of breast cancer survivors have shown that approximately 70 percent of the mutations identified were BRCA1/2 mutations. Approximately 4 percent had germline mutations in other cancer-susceptibility genes, including high-risk genes. These additional high-risk genes include CDH1, PALB2, PTEN, STK11, and TP53. Pathway Genomics’ BreastTrue High Risk Panel analyzes all of these genes.

“The development and launch of this breast cancer high risk panel is a necessity to effectively serve physicians and their patients,” said Jim Plante, Pathway Genomics’ founder and CEO. “Our mission is clear and precise. We exist to provide the most accurate and comprehensive genetic tests to the medical community, and we will continue to innovate.”

Conditions such as Li-Fraumeni, Cowden, Peutz-Jeghers, and hereditary diffuse gastric cancer (HDGC) syndromes have been associated with a significantly increased risk for breast cancer, and genetic testing of the genes associated with these conditions (i.e., TP53, PTEN, STK11 and CDH1) has been an important part of the clinical management of patients with a family history of breast cancer. Most recently, a large study published in the New England Journal of Medicine has also affirmed mutations in the PALB2 gene as important contributors to breast cancer risk.

“BreastTrue is the first breast cancer high risk panel in the industry that includes PALB2 full gene sequencing,” said Ardy Arianpour, Pathway Genomics’ chief strategy officer. “Cancer centers, genetic counselors and our current ordering clinicians have been asking us to deliver this type of product since our entry into this market.”

In addition to releasing BreastTrue High Risk Panel, Pathway has also enhanced its existing BRCATrueTM test to include single site, reflex testing, and BRCATrue Ashkenazi Jewish (3-site). The addition of reflex testing allows clinicians to appropriately utilize panel testing without creating unnecessary costs for patients and insurance companies.

To learn more about BreastTrue High Risk Panel with PALB2, visit www.pathway.com/breasttrue.

About Pathway Genomics Corporation
As a CLIA and CAP accredited clinical laboratory based in San Diego, California, Pathway Genomics provides physicians and their patients with actionable and accurate genetic information to improve or maintain health and wellness. Since its founding in 2008, Pathway Genomics has become known for its dedication to innovation and commitment to medical responsibility – making it a leader in the commercial genetic testing industry. Pathway Genomics’ testing services cover a variety of conditions including cancer risk, cardiac health, inherited diseases, nutrition and exercise response, as well as drug response for specific medications including those used in pain management and mental health. For more about Pathway Genomics, visit www.pathway.com.

Contacts

Pathway Genomics Corporation
Zak Pugh, 858-217-4358
pr@pathway.com
www.pathway.com

 

BreastTrue High Risk Panel is a blood or saliva next-generation sequencing test with deletion/duplication analysis to detect mutations in seven high-risk breast cancer susceptibility genes: BRCA1, BRCA2, CDH1, PALB2, PTEN, STK11, and TP53. (Graphic: Business Wire)

BreastTrue High Risk Panel is a blood or saliva next-generation sequencing test with deletion/duplication analysis to detect mutations in seven high-risk breast cancer susceptibility genes: BRCA1, BRCA2, CDH1, PALB2, PTEN, STK11, and TP53. (Graphic: Business Wire)