Does a targeted cfDNA-based MCED test accurately detect cancer compared to traditional biomarkers in adults?
3,988 participants aged ≥20 years with either confirmed cancer (n=2,342) or cancer-free status (n=1,646), focusing on cancers commonly seen in Asian populations.
Targeted multi-cancer early detection (MCED) test analyzing tumour-associated mutations in plasma cfDNA using machine learning models.
Traditional biomarkers such as CEA, and confirmed clinical status.
Diagnostic performance (sensitivity and specificity) for detecting 20 cancer types.surrogate
A targeted cfDNA-based MCED test demonstrated high sensitivity and specificity for detecting multiple cancer types, particularly those prevalent in Asia, offering a promising non-invasive screening tool.
Abstract Early cancer detection significantly improves survival, particularly for high-burden cancers across Asia that are often diagnosed late. Plasma-derived cell-free DNA (cfDNA) is a promising non-invasive biomarker for identifying cancer earlier than conventional methods. This study evaluated the performance of a targeted multi-cancer early detection (MCED) test that analyzes tumour-associated mutations in cfDNA to detect 20 cancer types commonly seen in Asian populations. In this retrospective, multicentre validation study, participants aged ≥20 years with either confirmed cancer or cancer-free status were recruited. Plasma cfDNA was sequenced using a targeted panel constructed from large genomic datasets. Machine learning models were trained and validated in a blinded manner to assess diagnostic performance. Among 2342 cancer cases and 1646 controls, the MCED test achieved a sensitivity of 83.1% (95% CI: 81.5-84.6%) and specificity of 95.4% (95% CI: 94.4-96.4%), with a false-positive rate of 4.6%. Performance surpassed that of traditional biomarkers such as CEA. Notably, high sensitivity was observed in cancers of major concern in Asia—liver, gastric, pancreatic, bile duct, and nasopharyngeal cancers—with early-stage detection ranging from 75.0-91.3% and late-stage detection from 95.5-100%. These findings support the potential of cfDNA-based MCED testing as a non-invasive, complementary screening approach for populations in Asia. Its strong performance across multiple high-mortality cancers underscores its value for early detection, risk stratification, and integration into regional cancer control strategies. Citation Format: Chee-Onn Leong, Boon Shing Tan, Hiu Ching Toh, Ee Mun Loo, Anand Mohan, Teryna Thu, Zhi Win Ng, Xin Yi Chew, Chin King Looi, Felicia Fei Lei Chung, Chun Wai Mai. Clinical validation of a targeted multi-cancer early detection (MCED) test using cfDNA mutation and integrated genomic signatures analysis abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1113.
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Chee-Onn Leong
Boon Shing Tan
Hiu Ching Toh
Cancer Research
International Medical University
University Kebangsaan Malaysia Medical Centre
University of Kuala Lumpur
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Leong et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fd3da79560c99a0a3298 — DOI: https://doi.org/10.1158/1538-7445.am2026-1113