Myriad Genetics Announces Reorganization of European Operations and Sale of EndoPredict Business – Read more
HRD status provides a valuable predictive marker for PARPi effectiveness, but many patients may be missed by BRCA1 & 2 testing or assays measuring loss of heterozygosity alone.1,2,6-8
HRD testing has life-changing consequences for every woman with ovarian cancer, and MyChoice® is here to guide treatment decisions for each one.
MyChoice® accurately identifies more HRD+ patients than tests that measure BRCA1 & 2 status or loss of heterozygosity alone,1,6-8 ensuring you have the most accurate information to make informed treatment decisions.
Local testing with MyChoice® allows easy ordering and fast results, supporting you to identify eligible patients for PARPi treatment in time.
MyChoice® is a trusted partner, as the only HRD test with FDA approval,9 CE certification, recommendation in major international treatment guidelines10-12 and the most prospective phase III study data.1-5
Somatic testing should prioritize identification of molecular alterations that inform the use of effective interventions. This includes assessing BRCA1/2, loss of heterozygosity (LOH), or homologous recombination deficiency (HRD) status in the absence of a germline BRCA mutation.
Myriad MyChoice® is included in the new recommendations from The American Society of Clinical Oncology (ASCO) on the use of PARP inhibitors for the treatment and management of certain patients with advanced ovarian cancer.
Validated scar-based HRD tests can be used to guide PARP inhibitor treatment. ESMO recognizes MyChoice® is the only scar based HRD test validated in the first-line maintenance setting.
Discover more about how MyChoice® works and why it helps you identify the right ovarian cancer patients for PARPi treatment in time.
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