Oncoseek 2.0: An updated blood-based assay for multi-cancer early detection.

S Shiyong Li M Mao Mao Y Yong Shen (MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry) W Wei Wu Y Yinyin Chang (9Clinical Laboratories, Shenyou Bio, Zhengzhou, China) P Pingping Xing C Chenyu Ding (9Clinical Laboratories, Shenyou Bio, Zhengzhou, China) D Dandan Zhu Q Qingxia Xu W Wei Cui (Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University)

Abstract

10551 Background: Early identification of cancer remains essential for improving survival and reducing downstream treatment costs, yet effective and scalable multi-cancer screening strategies are still limited. OncoSeek is a previously validated, AI-based multi-cancer early detection (MCED) assay integrating protein tumor markers (PTMs) with clinical data, demonstrating 58.4% sensitivity, 92.0% specificity, and 70.6% tissue-of-origin accuracy in > 15,000 participants. To improve detection of specific cancer types and expand cancer-type coverage, we developed OncoSeek 2.0 by incorporating three additional PTMs and evaluated its performance in validation cohort. Methods: OncoSeek 2.0 retained the original machine-learning framework of OncoSeek 1.0, with expanded PTM inputs (ProGRP, SCCA, and tPSA). Performance was evaluated in a retrospective validation cohort comprising 1,267 cancer and 355 non-cancer individuals. Overall performance, including cancer-type-specific sensitivity, was assessed and compared with OncoSeek 1.0. Results: OncoSeek 2.0 incorporated three additional PTMs (ProGRP, SCCA, and tPSA) to enhance cancer-type–specific detection. ProGRP levels was significantly elevated in small cell lung cancer compared with other cancers and healthy controls; SCCA concentrations were higher in squamous cell carcinomas (esophageal, cervical, and lung) than in non-squamous cancers and controls; and tPSA was selectively increased in prostate cancer (all P < 0.0001). Compared with OncoSeek 1.0, OncoSeek 2.0 achieved a higher AUC (0.917 vs 0.860) and improved sensitivity from 65.3% to 77.6% at 90.1% specificity across 15 pre-specified cancer types collectively accounting for 76.5% of global cancer mortality. Sensitivity gains were notable in lung (75.1% → 84.3%), prostate (58.8% → 88.2%), cervical (55.6% → 65.6%), and esophageal (39.6% → 62.4%) cancers. When stratified by tumor stage, OncoSeek 2.0 achieved sensitivities of 54.2% for stage I, 71.7% for stage II, 79.8% for stage III, and 88.4% for stage IV, consistently outperforming OncoSeek 1.0, which achieved sensitivities of 30.2%, 53.8%, 62.3%, and 85.7% for stages I through IV, respectively. Conclusions: By integrating three additional cancer-type–specific PTMs, OncoSeek 2.0 substantially improves sensitivity while maintaining high specificity and low reagent cost (~$30 per test). The upgraded assay enhances detection across multiple tumor types and disease stages, with particularly pronounced gains in lung, prostate, cervical, and esophageal cancers. These results support OncoSeek 2.0 as a scalable and clinically actionable MCED approach for population-level early detection, particularly for cancers lacking USPSTF-recommended screening and in low- and middle-income countries.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 10551-10551
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

S

Shiyong Li

M

Mao Mao

Y

Yong Shen

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry

W

Wei Wu

Y

Yinyin Chang

9Clinical Laboratories, Shenyou Bio, Zhengzhou, China

P

Pingping Xing

C

Chenyu Ding

9Clinical Laboratories, Shenyou Bio, Zhengzhou, China

D

Dandan Zhu

Q

Qingxia Xu

W

Wei Cui

Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University