American Association for Cancer Research
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Supplementary Table S2 from Detection of Early-Stage Colorectal Cancer Using Cell-Free oncRNA Biomarkers and Artificial Intelligence

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posted on 2025-08-01, 07:22 authored by Amir Momen-Roknabadi, Mehran Karimzadeh, Nae-Chyun Chen, Taylor B. Cavazos, Jieyang Wang, Jeremy Ku, Alex Degtiar, Akshaya Krishnan, Martha Hernandez, Magdalena Gebala, Alice Huang, Selina Chen, Dang Nguyen, Ti Lam, Rose Hanna, Lisa Fish, Alexx J. Smith, Sukh Sekhon, Jennifer Yen, Jeff Gregg, Helen Li, Fereydoun Hormozdiari, Babak Behsaz, Anna Hartwig, Hani Goodarzi, Lee Schwartzberg, Babak Alipanahi
<p>Supplementary Table S2. Validation set sensitivity and specificity across confounders</p>

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ARTICLE ABSTRACT

Colorectal cancer is the second leading cause of cancer-related deaths worldwide, and early detection significantly improves treatment outcomes, but existing blood-based tests often have limited sensitivity in early-stage disease. We developed a blood-based test combining orphan noncoding RNAs (oncRNA), a group of small cell-free RNAs, with generative artificial intelligence to detect colorectal cancer. We leveraged a cohort of 613 colorectal cancer cases and controls to train a model that demonstrated both high clinical performance and minimal technical variability in robustness testing. We further validated our model in an independent, single-source cohort of 192 colorectal cancer cases and controls. Model performance was assessed by sensitivity, specificity, and area under the ROC curve, with attention to early-stage detection. In our independent validation set, we achieved an overall sensitivity of 89% at 90% specificity, with an 80% sensitivity for stage I—an important milestone, as early-stage colorectal cancer detection remains a challenge for other blood-based technologies. Performance was consistent across demographic subgroups. Our oncRNA–based blood test, powered by artificial intelligence, offers strong performance for early colorectal cancer detection, including in stage I disease for which existing blood-based assays are limited. These findings support further development toward a minimally invasive colorectal cancer screening tool.