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Natera Presents Updated Analyses From ALTAIR Clinical Trial at ASCO GI

Key Takeaway: Natera, Inc. announced updated analyses from the ALTAIR clinical trial, which demonstrated a statistically significant disease-free survival (DFS) benefit for patients treated with Trifluridine/Tipiracil compared to placebo. This new data will be presented at the ASCO GI symposium in January 2026. The findings mark a significant improvement over earlier results that did not achieve statistical significance.
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POSITIVE FACTORS

  • Statistically significant DFS benefit observed in Signatera-positive patients.
  • New analysis provides substantial updates from previous ALTAIR findings.
  • Natera's presentations at ASCO GI highlight innovative research in cancer management.

Full Press Release Details

Study showed a statistically significant disease-free survival (DFS) benefit in all SignateraTM-positive patients following blinded central review
AUSTIN, Texas--(BUSINESS WIRE)--Natera, Inc.(NASDAQ: NTRA), a global leader in cell-free DNA and precision medicine, today announced that new data from the ALTAIR trial will be presented at the 2026 American Society of Clinical Oncology Gastrointestinal Cancers Symposium (ASCO GI), taking place January 8-10, 2026.
A new analysis will be presented from the randomized, double-blind, phase III ALTAIR clinical trial (NCT04457297). ALTAIR examined treatment on molecular recurrence (TOMR) with Trifluridine/Tipiracil (FTD/TPI) in Signatera-positive patients with stage I-IV colorectal cancer (CRC). This investigator-initiated analysis, based on a post-hoc blinded central radiographic review that resulted in the reclassification of a subset of cases, showed a statistically significant DFS benefit of FTD/TPI vs. placebo in all patients (median DFS 9.23 vs 5.55 months; HR: 0.75, 95% CI: 0.55-0.98; P=0.0406). Importantly, these findings represent a substantial update from the previously reported overall ALTAIR analysis, which showed a numerical DFS improvement that did not reach statistical significance in the full study population.
In addition to ALTAIR, Natera’s ASCO GI presentations include a large-scale study on Signatera velocity as a prognostic marker for relapse risk stratification. In the study, CRC patients whose Signatera levels doubled in one month or less experienced ~40% shorter recurrence free survival (RFS) vs patients with slower doubling time. The prognostic association between the rate of circulating tumor DNA (ctDNA) increase and recurrence risk remained significant for patients who received adjuvant chemotherapy, as well as those who did not. This data is specific to Natera’s quantification method, which uses mean tumor molecules (MTM) per mL of plasma.
“Natera’s unmatched scale of evidence across tumor types uniquely positions the company to define ctDNA dynamics and translate them into meaningful biological insight and clinical action,” said Adham Jurdi, M.D., senior medical director of GI oncology at Natera. “We believe these capabilities, including TOMR approaches, can ultimately support more precise risk stratification and cancer management.”
The full list of 14 presentations at ASCO GI includes:
January 8, 11:30 AM PT | Abstract # 440Presenter: Sahar Forootan SedighTumor-informed ctDNA monitoring during surveillance for early detection of recurrence in patients with stage II/III esophageal cancer treated with chemoradiation
January 8, 11:30 AM PT | Abstract # 843Presenter: Axel Grothey, M.D.AI-assisted automated abstraction for enhanced patient insights in gastrointestinal cancers
January 8, 11:30 AM PT | Abstract # 814Presenter: Gladys Magaly Rodriguez, M.D., MSCharacterization of DPYD variants across ancestries in a large real-world cohort of cancer patients
January 9, 11:30 AM PT | Abstract # 778Presenter: Elishama Kanu, M.D., MAPrognostic value of ctDNA monitoring in patients with resectable pancreatic ductal adenocarcinoma during surveillance
January 10, 7:00 AM PT | Abstract # 163Presenter: George Q. Zhang, M.D., MPHPhysical activity and molecular residual disease (MRD) in stage III colon cancer: Findings from CALGB (Alliance)/SWOG 80702
January 10, 7:00 AM PT | Abstract # 216Presenter: Saori Mishima, M.D., Ph.D.Assessing adjuvant chemotherapy benefit in younger and older molecular residual disease-positive patients with stage II/III colorectal cancer
January 10, 7:00 AM PT | Abstract # 221Presenter: Naoya Akazawa, M.D.Prognostic value of presurgical circulating tumor DNA (ctDNA) levels and other clinical factors in colon cancer
January 10, 7:00 AM PT | Abstract # 220Presenter: Koji AndoCorrelation between the timing of recurrence and circulating tumor DNA (ctDNA) doubling time in patients (pts) with resected colon cancer
January 10, 7:00 AM PT | Abstract # 153Presenter: Kozo Kataoka, M.D., Ph.D.Adjuvant mFOLFOXFIRI after curative-intent resection of oligometastatic colorectal cancer: Phase II FANTASTIC trial
January 10, 7:00 AM PT | Abstract # TPS268Presenter: Anwaar Saeed, M.D.NSABP FC-13 (EMPIRE): A phase II platform study of cemiplimab monotherapy or cemiplimab-based combinations in patients with colorectal cancer and minimal residual disease (MRD) after definitive therapy
January 10, 7:00 AM PT | Abstract # 138Presenter: Jun Watanabe, M.D., Ph.D.Post-hoc central radiological review of the ALTAIR study in patients with molecular residual disease (MRD) following curative resection of colorectal cancer (CRC)
January 10, 7:00 AM PT | Abstract # TPS245Presenter: Sarah Sawyer, Ph.D.Design of a hybrid site and decentralized clinical research study of an early detection blood test for colorectal cancer
January 10, 7:00 AM PT | Abstract # 217Presenter: Yoshiaki Nakamura, M.D., Ph.D.Quantification of circulating tumor DNA (ctDNA) using a methylation-based, tissue-free colorectal cancer (CRC) test for the detection of molecular residual disease (MRD)
January 10, 11:30 AM PT | Abstract # 12 (Oral Presentation)Presenter: Hideaki Bando, M.D., Ph.D.Impact of postoperative ctDNA dynamics on eligibility for the ALTAIR randomized trial in patients with colorectal cancer: Implications for clinical trial enrollment
About Natera
Natera™ is a global leader in cell-free DNA and precision medicine, dedicated to oncology, women’s health, and organ health. We aim to make personalized genetic testing and diagnostics part of the standard-of-care to protect health and inform earlier, more targeted interventions that help lead to longer, healthier lives. Natera’s tests are supported by more than 325 peer-reviewed publications that demonstrate excellent performance. Natera operates ISO 13485-certified and CAP-accredited laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas, and San Carlos, California, and through Foresight Diagnostics, its subsidiary, operates an ISO 27001-certified and CAP-accredited laboratory certified under CLIA in Boulder, Colorado. For more information, visitwww.natera.com.
Forward-Looking Statements
All statements other than statements of historical facts contained in this press release are forward-looking statements and are not a representation that Natera’s plans, estimates, or expectations will be achieved. These forward-looking statements represent Natera’s expectations as of the date of this press release, and Natera disclaims any obligation to update the forward-looking statements. These forward-looking statements are subject to known and unknown risks and uncertainties that may cause actual results to differ materially, including with respect to whether the results of clinical or other studies will support the use of our product offerings, the impact of results of such studies, our expectations of the reliability, accuracy and performance of our tests, or of the benefits of our tests and product offerings to patients, providers and payers. Additional risks and uncertainties are discussed in greater detail in “Risk Factors” in Natera’s recent filings on Forms 10-K and 10-Q and in other filings Natera makes with the SEC from time to time. These documents are available atwww.natera.com/investorsandwww.sec.gov.

Frequently Asked Questions

What is the ALTAIR clinical trial?

The ALTAIR trial is a randomized, double-blind, phase III study examining treatment on molecular recurrence in colorectal cancer patients.

What were the findings of the ALTAIR trial?

The trial showed a statistically significant disease-free survival benefit for patients treated with Trifluridine/Tipiracil compared to placebo.

When will the ALTAIR trial data be presented?

The updated data will be presented at the ASCO GI symposium from January 8-10, 2026.

What is Signatera in relation to the trial?

Signatera is a personalized ctDNA test used to monitor molecular recurrence in patients with colorectal cancer.

What does DFS stand for?

DFS stands for disease-free survival, a measure of the time after treatment during which a patient remains free of disease.

Last updated: Jan 6, 2026