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AI/ML-based miRNA signatures show diagnostic potential for early breast cancer detection

AI/ML-based miRNA signatures show diagnostic potential for early breast cancer detection
Photo by Pawel Czerwinski / Unsplash
Key Takeaway
Consider AI/ML miRNA signatures as investigational adjuncts for breast cancer detection pending prospective validation.

This systematic review and meta-analysis evaluated the diagnostic performance of artificial intelligence/machine learning (AI/ML)-based circulating microRNA (miRNA) signatures for detecting early breast cancer. The analysis pooled data from 7 studies, though the specific patient population size and study settings were not reported. No direct comparator was specified in the analysis.

The main results showed a pooled area under the curve (AUC) of 0.905 (95% CI: 0.890-0.921), indicating high overall diagnostic accuracy. The pooled sensitivity was 81.3% (95% CI: 76.8%-85.2%), and the pooled specificity was 87.0% (95% CI: 82.4%-90.7%). Safety and tolerability data were not reported in the available evidence.

Key limitations include significant methodological heterogeneity across the included studies, variable rigor in validation procedures, and a predominance of retrospective case-control designs, which can introduce bias. The funding sources and potential conflicts of interest were not reported.

In practice, these AI/ML-based miRNA signatures may have value as non-invasive adjunctive tools within imaging-supported diagnostic pathways. However, the authors caution that routine clinical implementation cannot be justified before prospective, standardized, and externally validated studies are completed. The current evidence, while promising, is insufficient to support a change in clinical practice.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMar 2026
View Original Abstract ↓
BackgroundEarly breast cancer detection remains central to improving clinical outcomes, yet conventional screening pathways, particularly mammography, have recognized limitations in sensitivity, specificity, and performance in dense breast tissue. Circulating microRNAs (miRNAs) have emerged as promising minimally invasive biomarkers, while artificial intelligence and machine learning (AI/ML) offer powerful tools for identifying diagnostically relevant multi-marker patterns within complex biomarker datasets. This systematic review and meta-analysis evaluated the diagnostic performance of AI/ML-based circulating miRNA signatures for early breast cancer detection. MethodsA systematic search of PubMed/MEDLINE, Scopus, and Web of Science Core Collection was conducted from database inception to 31 December 2025. Studies were eligible if they were original human investigations evaluating circulating miRNAs using an AI/ML-based diagnostic model for breast cancer detection and reporting extractable diagnostic performance metrics. Study selection followed PRISMA 2020 and PRISMA-DTA guidance. Methodological quality was assessed using QUADAS-2. Pooled sensitivity and specificity were synthesized using a bivariate random-effects model, and overall diagnostic performance was summarized using a hierarchical summary receiver operating characteristic framework. ResultsSeven studies met the inclusion criteria for qualitative synthesis, with eligible studies contributing to the quantitative analysis depending on data availability. Across the pooled analysis, AI/ML-based circulating miRNA models demonstrated good overall diagnostic performance, with a pooled AUC of 0.905 (95% CI: 0.890-0.921), pooled sensitivity of 81.3% (95% CI: 76.8%-85.2%), and pooled specificity of 87.0% (95% CI: 82.4%-90.7%). Heterogeneity was moderate for AUC (I{superscript 2} = 42.3%) and sensitivity (I{superscript 2} = 38.7%) and low for specificity (I{superscript 2} = 28.4%). Risk-of-bias assessment showed overall low-to-moderate methodological concern, with patient selection representing the most variable domain. Deeks funnel plot asymmetry test showed no significant evidence of publication bias (p = 0.34). ConclusionsAI/ML-based circulating miRNA signatures show promising diagnostic accuracy for early breast cancer detection and may have value as non-invasive adjunctive tools within imaging-supported diagnostic pathways. However, the evidence base remains limited by methodological heterogeneity, variable validation rigor, and the predominance of retrospective case-control designs. Prospective, standardized, and externally validated studies are needed before routine clinical implementation can be justified.
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