Personalis Pioneers Advancement in MRD Testing with the Launch of its Real-Time Variant Tracker™
New NeXT Personal® extension empowers clinicians to identify emerging resistance and therapeutically targetable mutations during disease monitoring and surveillance
Clinicians using the NeXT Personal MRD test will now be able to opt-in for additional reporting on detected resistance and therapeutically targetable mutations that can inform new opportunities to optimize patient management. This includes ESR1 mutations, which can be an indication to switch therapy for HR+/HER2- breast cancer patients, and hundreds of other clinically relevant mutations for solid tumors.
“Personalis pioneered the shift toward ultrasensitive MRD, and today we are once again taking another innovative step forward,” said
This new capability enables clinicians using the NeXT Personal MRD test to additionally monitor for:
- Emerging or evolving therapy resistance mutations that could impact clinical management
- Therapeutically targetable mutations associated with approved therapies
“The ability to detect evolving, clinically relevant mutations in genes like ESR1 during MRD monitoring and surveillance gives physicians a new tool to help optimize care,” said
Availability
The Real-Time Variant Tracker option for NeXT Personal is available to physicians who participate in the Early Access Program (EAP). The EAP is designed for clinical and academic leaders using NeXT Personal who are looking to integrate this new capability into their clinical practice and research. The ability to track mutations is also available to Personalis’ biopharma partners.
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Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include all statements that are not historical facts, including statements relating to: the attributes, advantages, capabilities, sensitivity, availability and clinical relevance of Personalis’ assays and products including the NeXT Personal test and the Real-Time Variant Tracker option, the ability for Real-Time Variant Tracker to identify emerging resistance and actionable targets, remain unique in its ability to monitor mutations, and inform new opportunities to optimize patient management, participation of physicians in the EAP and adoption of mutation tracking by Personalis’ biopharma partners, and the success of Personalis’ continued innovation in the MRD space. Such forward-looking statements involve known and unknown risks and uncertainties and other factors that may cause actual results to differ materially from any anticipated results or expectations expressed or implied by such statements, including the risks, uncertainties and other factors that relate to Personalis’ ability to demonstrate attributes, advantages or clinical validity of the NeXT Personal test and the Real-Time Variant Tracker option, the NeXT Personal MRD assay remaining unique in its ability to detect traces of cancer in the ultrasensitive range and its ability to monitor mutations; future clinical data differing from the clinical data previously presented or expected results; the rate of adoption and use of the NeXT Personal test and the Real-Time Variant Tracker option; changes in health care policy, which could increase Personalis’ costs, decrease Personalis’ revenue, and impact sales of and reimbursement for Personalis’ tests; the impact of competition and macroeconomic factors on Personalis’ business; the partnering and/or collaboration arrangements that
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