Six presented abstracts at ASCO-GU 2026 reinforce the clinical impact of Myriad’s Precise MRD, Prolaris, and MyRisk tests
Rhea-AI Summary
Myriad Genetics (NASDAQ: MYGN) will present six abstracts at ASCO-GU Feb 26-28, 2026 reporting clinical performance for Precise MRD, Prolaris, and MyRisk oncology tests. Key data include ultra-sensitive ctDNA detection (below 100 ppm), a meta-analysis of 14 studies >8,000 patients showing Prolaris prognostic power, and germline testing results across Gleason and NCCN risk groups.
Findings are largely interim or preliminary but indicate potential diagnostic and prognostic value across genitourinary cancers.
Positive
- Prolaris meta-analysis covers 14 studies >8,000 patients
- Precise MRD detects ctDNA in the ultrasensitive range <100 ppm
- Prolaris prognostic for distant metastasis and prostate-cancer mortality
Negative
- Most results are interim or from maturing trials, limiting clinical certainty
- Early evidence shows correspondence between ctDNA and outcomes but is not definitive
News Market Reaction – MYGN
On the day this news was published, MYGN gained 1.14%, reflecting a mild positive market reaction. Argus tracked a peak move of +9.8% during that session. Our momentum scanner triggered 13 alerts that day, indicating notable trading interest and price volatility. This price movement added approximately $5M to the company's valuation, bringing the market cap to $408M at that time.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Market Reality Check
Peers on Argus
MYGN is up 2.1% on strong ASCO-GU clinical data while scanner activity shows peer CDNA down 2.61% with no news, pointing to a stock-specific move rather than a sector-wide rotation.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Feb 23 | Earnings and guidance | Positive | +2.1% | Reported Q4 and 2025 results and reiterated 2026 revenue and EBITDA guidance. |
| Feb 19 | Clinical validation news | Positive | -0.3% | Published analytical validation for FirstGene prenatal screen with high sensitivity and specificity. |
| Feb 16 | Earnings date notice | Neutral | +0.2% | Announced timing and webcast details for upcoming Q4 and full-year 2025 results. |
| Jan 27 | MRD commercialization plan | Positive | +1.9% | Outlined March 2026 limited launch of Precise MRD backed by strong ctDNA sensitivity data. |
| Jan 12 | Prelim results, guidance | Positive | -0.1% | Released preliminary Q4/2025 revenue ranges and introduced 2026 revenue and EBITDA guidance. |
Recent fundamentally positive updates (earnings, MRD data, product validation) have more often seen modestly positive price alignment, but there are instances where favorable clinical or guidance news was followed by flat-to-negative reactions.
Over the past several weeks, Myriad reported Q4 2025 results with $209.8M revenue and reiterated 2026 guidance, highlighted new data and commercialization steps for Precise MRD, and published validation for the FirstGene prenatal screen. Preliminary 2025 trends and 2026 guidance were first outlined in January. Today’s ASCO-GU abstracts extend the same oncology testing narrative, reinforcing earlier MRD performance data and underscoring the role of Prolaris and MyRisk within prostate and genitourinary cancer care.
Market Pulse Summary
This announcement underscores Myriad’s focus on oncology diagnostics, highlighting Precise MRD, Prolaris, and MyRisk across bladder, urothelial, renal, and prostate cancers. Meta-analysis data spanning 14 studies and over 8,000 patients and ultrasensitive ctDNA detection below 100 parts per million reinforce test performance claims. Investors may track future updates on clinical outcomes correlations, guideline or payer adoption, and how these platforms contribute to the reiterated 2026 growth and profitability framework outlined in recent earnings disclosures.
Key Terms
molecular residual disease medical
ctdna medical
meta-analysis technical
prognostic medical
germline medical
gleason score medical
nccn risk grouping medical
whole-genome sequencing medical
AI-generated analysis. Not financial advice.
SALT LAKE CITY, Feb. 24, 2026 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc., (NASDAQ: MYGN), a leader in molecular diagnostic testing and precision medicine, will present new data at the 2026 ASCO-GU conference supporting its Precise MRDTM (Molecular Residual Disease) Test, Prolaris® Prostate Cancer Prognostic Test and MyRisk® Hereditary Cancer Tests. These data highlight Myriad’s expanding role across the cancer care continuum, including ultra-sensitive molecular residual disease detection, prognostic stratification, and inherited cancer risk assessment.
“The data Myriad is presenting at ASCO-GU suggest our oncology products go further than standard approaches to deliver unique insights for patients with cancer,” said Dale Muzzey, PhD, Chief Scientific Officer, Myriad Genetics. “Our MRD test may reveal clinically consequential information that may not have been attainable on first-generation tests. We demonstrate with deep statistical rigor that Prolaris is highly prognostic and additive to classical risk categories. Finally, we find that MyRisk has comparable likelihood to identify a germline variant across risk groups, which may help to broaden the scope of those who receive and benefit from testing.”
Multiple studies presented at ASCO-GU will highlight the performance of Precise MRD in genitourinary cancers, including bladder cancer, urothelial cancer, and renal cell carcinoma. In these analyses, sensitivity was high at the baseline time point, with many detection events at ctDNA concentrations in the ultrasensitive range below 100 parts per million. Though the trials are still maturing, the early evidence to be presented at ASCO-GU suggests a correspondence between ctDNA levels and clinical outcomes.
The company will share results of a robust meta-analysis of 14 studies involving more than 8,000 patients that support the prognostic power of the Prolaris Prostate Cancer Prognostic Test. The meta-analysis indicates that Prolaris is significantly prognostic for both distant metastasis and prostate-cancer specific mortality. These data help explain why Prolaris is uniquely suited to help guide initial treatment decisions. Importantly, Prolaris was found to be significantly prognostic above and beyond conventional risk categories driven by clinical factors alone.
Finally, data will be presented evaluating germline testing using the MyRisk Hereditary Cancer Test in localized prostate cancer, including the prevalence of pathogenic variants and their association with Gleason score and NCCN risk grouping. The data indicate that germline positivity rates do not significantly differ across the Gleason-score groups or NCCN risk groups, suggesting that it may not be appropriate to limit germline testing only to those with high Gleason or NCCN risk.
These abstracts and posters will be presented at the American Society of Clinical Oncology (ASCO) Genitourinary Cancers Symposium, which will be held Feb. 26-28 at the Moscone West Conference Center, San Francisco, Calif., Myriad will exhibit at booth #20. For more information, visit: https://myriad.com/oncology/conferences/
Myriad Genetics Presentations
Precise MRD
Ultra-sensitive molecular residual disease detection via tumor-informed whole-genome sequencing-based ctDNA assay in resectable urothelial cancer in the MONSTAR-SCREEN-3 project
Poster Board Number: J16; Abstract Number: 810
Friday, Feb. 27 11:30 AM - 12:45 PM PST, 4:45 PM - 5:45 PM PST
Presenter: Shigehiro Tsukahara, Kyushu University, Fukuoka, Japan
CONSOLIDATE: Interim Results from a Phase I/II study of radiotherapy combined with enfortumab vedotin (EV) for locally advanced bladder cancer with paired translational ctDNA and utDNA
Poster Board Number: N25; Abstract Number: TPS912
Friday, Feb. 27 11:30 AM - 12:45 PM PST; 4:45 PM - 5:45 PM PST
Presenter: Patrick Carriere, MD, MD Anderson Cancer Center
Circulating KIM-1 and ctDNA as prognostic markers in oligometastatic clear cell renal cell carcinoma (ccRCC): The K-COMPASS model
Rapid Oral Abstract; Abstract Number: 537
Saturday, Feb. 28, 12:45 PM - 1:30 PM PST
Presenter: Chad Tang, MD, The University of Texas MD Anderson Cancer Center
Ultra-sensitive whole-genome sequencing-based molecular residual disease detection in resectable renal cell carcinoma: Preliminary results from the MONSTAR-SCREEN-3 study
Rapid Oral Abstract; Abstract Number: 421
Saturday, Feb. 28, 12:45 PM - 1:30 PM PST
Presenter: Taigo Kato, MD, PhD, Osaka University, Osaka, Japan
Prolaris Prostate Cancer Prognostic Test
The Prolaris Test on diagnostic biopsy for localized prostate cancer prognosis across risk groups and management: An individual participant data meta-analysis
Poster Board Number: M22; Abstract Number: 394
Thursday, Feb. 26, 11:30 AM - 12:45 PM PST and 5:45 PM - 6:45 PM PST
Presenter: Steven Monda, MD, University of Michigan
MyRisk Hereditary Cancer Test
Rethinking germline testing in localized prostate cancer: Prevalence of germline variants and association with Gleason score and NCCN risk grouping
Poster Board Number: K14; Abstract Number: 322
Thursday, Feb. 26, 11:30 AM - 12:45 PM PST and 5:45 PM - 6:45 PM PST
Presenter: Adam Cole, MD, TruCore Pathology
About Myriad Genetics
Myriad Genetics is a leading molecular diagnostic and precision medicine company committed to advancing health and well-being for all. Myriad Genetics develops and commercializes molecular tests that help patients and providers uncover genetic insights. Myriad Genetics tests assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where molecular insights can significantly improve patient care, support earlier detection, enable more precise treatment and contribute to lowering healthcare costs. For more information, visit www.myriad.com.
Myriad Genetics Safe Harbor Statement
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements about the company’s intent to present new data at the 2026 ASCO-GU conference regarding its Precise MRD, Prolaris and MyRisk tests, and that these data are expected to highlight Myriad’s expanding role across the cancer care continuum, including ultra-sensitive molecular residual disease detection, prognostic stratification, and inherited cancer risk assessment. These “forward-looking statements” are management’s expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10-K filed on February 28, 2025, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise except as required by law.
Investor Contact
Matt Scalo
(801) 584-3532
IR@myriad.com
Media Contact
Kate Schraml
(224) 875-4493
PR@myriad.com