Exact Sciences Announces Expanded Clinical Validation of the Oncodetect™ Test and Molecular Residual Disease Innovation Roadmap
May 28 2025 - 6:05AM
Business Wire
Beta-CORRECT study to be presented at ASCO 2025
confirms the clinical utility of the molecular residual disease
(MRD) test, Oncodetect™, for recurrence monitoring in stage II–IV
colorectal cancer
Whole-genome Oncodetect test powered by MAESTRO
to launch in 2026 with ultra-low limit of detection1
Exact Sciences Corp. (NASDAQ: EXAS), a leading provider of
cancer screening and diagnostic tests, today announced new data to
be presented from the Beta-CORRECT clinical validation study at the
2025 American Society of Clinical Oncology (ASCO) Annual Meeting.
Results from Beta-CORRECT, a subset of the GALAXY cohort, validate
the performance of its tumor-informed molecular residual disease
(MRD) test, Oncodetect™, in predicting recurrence in stage II–IV
colorectal cancer. These data confirm the test’s role in supporting
treatment and surveillance decisions.
Building on this momentum and its commitment to innovation,
Exact Sciences will introduce a next-generation version of the test
leveraging the Broad Institute’s MAESTRO technology. Early data
show the test will track up 5,0002 patient specific variants and
detect ctDNA* levels below 1 part per million.1 The test will be
available to both new and existing customers in 2026.
“We launched the Oncodetect test to give clinicians and patients
a powerful tool for detecting cancer recurrence earlier and with
greater precision—progress that’s already being realized,” said
Brian Baranick, Executive Vice President and General Manager,
Precision Oncology at Exact Sciences. “We continue to innovate and
look forward to introducing the next iteration of the Oncodetect
test, which leverages whole-genome sequencing and proprietary
technology developed in collaboration with the Broad Institute to
enhance sensitivity and expand clinical utility.”
The Beta-CORRECT study demonstrates that the Oncodetect test
significantly improves prognosis prediction compared to traditional
standard of care methods †,3,4,5
Data presented at ASCO from the Beta-CORRECT clinical validation
study confirm that the Oncodetect test accurately predicts
recurrence in stage III colorectal cancer3—consistent with findings
from the Alpha-CORRECT study—and extends this association to stages
II and IV.4
Exact Sciences’ largest MRD clinical study to date, with more
than 400 patients, demonstrates those with ctDNA-positive results
after therapy and during surveillance showed a 24- and 37-fold
increased risk of recurrence, respectively.4 By quantifying ctDNA
levels across multiple timepoints, the Oncodetect test enables
physicians to more effectively guide treatment decisions and
surveillance strategies in clinical practice.3,4
Advancing the Oncodetect test with next generation
innovation
The next-generation MRD test, currently in validation across
multiple solid tumor types, will track up to 5,000 patient-specific
variants2 with a limit of detection below 1 part per million,1
enabling scalable monitoring and broad clinical utility. Exact
Sciences holds exclusive rights to the Broad Institute’s MAESTRO
technology, a whole-genome sequencing method able to detect
low-frequency ctDNA mutations with high accuracy. This technology
advances the ability to look broadly across thousands of mutations
while reducing the sequencing depth required to achieve an
ultra-low limit of detection at a highly attractive cost point.
Through continued innovation in MRD, Exact Sciences is advancing
solutions with the potential to change clinical practice.
“The precision and sensitivity seen in the next generation test
reflect deep scientific collaboration and a shared commitment to
advancing MRD technology,” said Viktor Adalsteinsson, Ph.D.,
Director, Gerstner Center for Cancer Diagnostics at the Broad
Institute. “This approach to innovation will continue to raise the
bar for recurrence monitoring, treatment response assessment, and,
ultimately, patient outcomes.”
* Circulating tumor DNA
† Standard of care markers include CEA and clinicopathologic
factors
References:
- Edward S. Sim, Justin Rhoades, Kan Xiong, Laurel Walsh, Andjela
Crnjac, Timothy Blewett, Yana Al-Inaya, Julia Mendel, Daniel A.
Ruiz-Torres, Vasileios Efthymiou, Gjystina Lumaj, William J.
Benjamin, G. Mike Makrigiorgos, Shervin Tabrizi, Viktor A.
Adalsteinsson, Daniel L. Faden; Early Postoperative Minimal
Residual Disease Detection with MAESTRO Is Associated with
Recurrence and Worse Survival in Patients with Head and Neck
Cancer. Clin Cancer Res 2025;
https://doi.org/10.1158/1078-0432.CCR-25-0307
- Data source on file. Exact Sciences. Madison, WI. May
2025.
- Diergaarde B, Young G, Hall DW, et al. Circulating tumor DNA as
a marker of recurrence risk in stage III colorectal cancer: the
α-CORRECT study. J Surg Oncol. Jan 2025.
- Hashimoto et. al: The Association of ctDNA with Recurrence in
Patients with Stage II-IV Colorectal Cancer: The ꞵ-CORRECT study.
Presented at ASCO 2025.
- ASCO 2025 Industry Expert Theater Presentation: Molecular
Residual Disease Testing with Exact Sciences’ Oncodetect test:
Product and Clinical Data Overview.
About Exact Sciences Corp.
A leading provider of cancer screening and diagnostic tests,
Exact Sciences helps give patients and health care professionals
the clarity needed to take life-changing action earlier. Building
on the success of the Cologuard® and Oncotype DX® tests, Exact
Sciences is investing in its pipeline to develop innovative
solutions for use before, during, and after a cancer diagnosis. For
more information, visit ExactSciences.com, follow Exact Sciences on
X (formerly known as Twitter) @ExactSciences, or find Exact
Sciences on LinkedIn and Facebook.
Oncodetect and Oncotype DX are trademarks of Genomic Health,
Inc., a wholly owned subsidiary of Exact Sciences. Exact Sciences
and Cologuard are trademarks of Exact Sciences Corporation.
Oncodetect is only available in the United States.
Forward-Looking Statement
This news release contains forward-looking statements concerning
our expectations, anticipations, intentions, beliefs, or strategies
regarding the future. These forward-looking statements are based on
assumptions that we have made 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 from
those anticipated. Therefore, you should not place undue reliance
on forward-looking statements. Examples of forward-looking
statements include, among others, statements regarding our
expectations for the commercialization of the Oncodetect and
next-generation MRD tests, the performance characteristics and
health care benefits of the Oncodetect and next-generation MRD
tests in a commercial setting, and launch date for the
next-generation MRD test. Risks and uncertainties that may affect
our forward-looking statements are described in the Risk Factors
sections of our most recent Annual Report on Form 10-K and any
subsequent Quarterly Reports on Form 10-Q, and in our other reports
filed with the Securities and Exchange Commission. We undertake no
obligation to publicly update any forward-looking statement,
whether written or oral, that may be made from time to time,
whether as a result of new information, future developments or
otherwise.
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version on businesswire.com: https://www.businesswire.com/news/home/20250528855786/en/
Media Contact: Lisa Warshaw +1 323-360-8778
lwarshaw@exactsciences.com
Investor Contact: Derek Leckow +1 608-893-0009
investorrelations@exactsciences.com
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