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Signatera™ for Ovarian Cancer

Move beyond the limitations of CA-125 and imaging.

Signatera™ provides a personalized, tumor-informed ctDNA assay that detects molecular residual disease (MRD), allowing you personalize treatment decisions for your ovarian cancer patients.

Powering clinical decisions in ovarian cancer

Test

Understand risk

23%

of patients were found with detectable ctDNA, all of whom experienced disease progression.1

Know

Detect recurrence earlier

100%

sensitivity and specificity longitudinally vs 43% and 78% respectively for CA-1251,2

Decide

Predict treatment response

98%

of patients who experienced an increase in ctDNA did not derive an objective response to treatment (after 2 cycles)3

Identify patients at risk of progression PARPi maintenance

Monitoring with Signatera™ can provide earlier insights into therapeutic response and potentially help guide treatment decisions by:

  • Identifying non-responders early
  • Escalating imaging when warranted

Monitor your patients with confidence

As part of her ovarian cancer monitoring plan, Anne received Signatera™ testing and CA-125 at regular intervals.

A positive Signatera™ result alerted her oncologist to order a scan, which caught a recurrence early. Now, Anne is receiving Signatera™ to monitor response to her maintenance therapy. Since starting therapy, Anne’s Signatera™ results have been negative, so she can feel more confident about her treatment plan.

Discover more data in ovarian cancer

Post-adjuvant MRD assessment

After completion of adjuvant/definitive therapy, ctDNA was detectable in 23% of patients, all of whom experienced disease progression.¹

Surveillance/maintenance

Longitudinally, ctDNA was detected with 100% sensitivity and specificity, while CA-125 had much lower sensitivity (43%) and specificity (78%).1,2

Treatment response monitoring

Signatera™ can help identify response to immunotherapy as early as 6 weeks into treatment in gynecologic cancers.³*

Tailor ovarian cancer treatment with Natera’s portfolio of genomic tests

Altera™ comprehensive genomic profiling (CGP)

Altera™ looks at tumor biomarkers and genomic changes that may help inform treatment planning and clinical trial discussions.

Empower™ hereditary cancer testing

Empower™ is a germline genetic test that looks for inherited cancer risk genes that may be relevant in gynecologic cancers. It may be considered based on your personal history and family history.

Is Signatera™ for ovarian cancer right for your patients?

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References

1Hou JY, et al. Gynecologic Oncology. 2022;167:334-341.

2Chapman et al. Poster presented at 2021 AACR Annual Meeting.

3Bratman et al. Nature Cancer. 2020;1(9):873-881.

4Toboni M, et al. Gynecologic Oncology. 2026;204:37–43.

Footnotes

*Includes high grade serous ovarian cancer (n=18), endometrial cancer (n=2), and cervical cancer (n=1).

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