Performance of a Cell-Free DNA-Based Multi-cancer Detection Test in Individuals Presenting With Symptoms Suspicious for Cancers

Author:

Bryce Alan H.1ORCID,Thiel David D.2,Seiden Michael V.3,Richards Donald4,Luan Ying5,Coignet Marie5ORCID,Zhang Quan5,Zhang Nan5,Hubbell Earl5ORCID,Kurtzman Kathryn N.5ORCID,Klein Eric A.56ORCID

Affiliation:

1. Mayo Clinic, Phoenix, AZ

2. Mayo Clinic Florida, Jacksonville, FL

3. US Oncology Research, The Woodlands, TX

4. US Oncology Research, Tyler, TX

5. GRAIL, LLC, Menlo Park, CA

6. Glickman Urological & Kidney Institute, Cleveland Clinic, Cleveland, OH

Abstract

PURPOSE A multi-cancer detection test using a targeted methylation assay and machine learning classifiers was validated and optimized for screening in prospective, case-controlled Circulating Cell-free Genome Atlas (ClinicalTrials.gov identifier: NCT02889978 ) substudy 3. Here, we report test performance in a subgroup of participants with symptoms suspicious for cancer to assess the test's ability to potentially facilitate efficient diagnostic evaluation in symptomatic individuals. METHODS We evaluated test performance (sensitivity, specificity, and accuracy of cancer signal origin [CSO] prediction accuracy) in participants with clinically presenting cancers (CPCs) and noncancer with underlying medical conditions and among two subgroups (65 years and older and GI cancers). Overall survival (OS) of participants who had a cancer signal detected/not detected was compared with SEER-based expected survival. RESULTS A total of 2,036 cancer and 1,472 noncancer participants were included. Specificity was high in all noncancer participants (99.5% [95% CI, 98.4 to 99.8]). In participants with CPCs, the overall sensitivity was 64.3% (95% CI, 62.2 to 66.4) and the overall accuracy of CSO prediction in true positives was 90.3%. For GI cancers, the overall sensitivity was 84.1% (95% CI, 80.6 to 87.1). In participants 65 years and older, test performance was similar to that of all participants. Individuals with cancers not detected had a significantly better OS than that expected from SEER ( P < .01). CONCLUSION This test detected a cancer signal with high specificity and CSO prediction accuracy and moderate sensitivity in symptomatic individuals, with especially high performance in participants with GI cancers. The survival analysis implied that the cancers not detected were less clinically aggressive than cancers detected by the test, providing prognostic insights to physicians. This multi-cancer detection test could facilitate efficient workup and stratify cancer risk in symptomatic individuals.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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