Patient Education

PATIENT EDUCATION FOR HEREDITARY CANCER GENETIC TESTING

For Patient Brochures and Patient Guides click on a product below:


Hereditary Cancer

myRisk2

myRisk
Myriad myRisk Hereditary Cancer is a 25-gene panel for the identification of clinically significant mutations impacting inherited risks for eight important cancers. Blending genetic test status AND personal/family cancer history into clinically significant risk assessment and follow-up, the myRisk Hereditary Cancer test represents the next generation of cancer genetic testing.

Hereditary Breast and Ovarian Cancer


bracanalysis

BRACAnalysis testing assesses a person’s risk of developing hereditary breast or ovarian cancer based
on the detection of mutations in the BRCA1 and BRCA2 genes.


Hereditary Colorectal Cancer


colaris

COLARIS testing assesses a person’s risk of developing hereditary colorectal cancer and a woman’s
risk of developing hereditary uterine/endometrial cancer by detecting disease-causing mutations in
the MLH1, MSH2, MSH6, PMS2, EPCAM and MYH genes.



colarisAp

COLARIS AP testing assesses a person’s risk of developing hereditary colorectal polyps and cancer by
detecting mutations in the APC and MYH genes.


Prognostic gene expression panels in cancer: Breast Cancer

endo
Logo_EndoPredict

EndoPredict is a second generation gene expression analysis used to determine the risk of metastasis with
endocrine therapy alone in patients with ER-positive HER2-negative primary breast cancer. Stratifying
patients into clear High and Low Risk categories, EndoPredict reliably predicts early and late metastases.


Prostate Cancer


prolaris

Prolaris is a molecular diagnostic test that measures the expression level of genes involved with
tumor proliferation to predict disease outcome. Prolaris can be used in conjunction with other
clinical parameters to determine prostate cancer aggressiveness. The Prolaris result provides
10-year risks for prostate cancer specific mortality in the biopsy setting or biochemical recurrence
in the post-prostatectomy setting.


Companion Diagnostics

comp
tumor_logo

Tumor BRACAnalysis CDx is a CE marked companion diagnostic tumor test for ovarian cancer patients.
This test can detect up to 50% more patients with mutations in the BRCA1 and BRCA2 genes. BRCA
mutation analysis is essential in ovarian cancer patients to identify the subset of women who are
most likely to benefit from PARP inhibitors.



branc_logo

BRACAnalysis is a companion diagnostic blood test for ovarian cancer patients, to detect germline
mutations in the BRCA1 and BRCA2 genes. BRCA mutation analysis is essential in ovarian cancer
patients to identify the subset of women who are most likely to benefit from PARP inhibitors.