ReviewBreast cancer (Dove Medical Press)2025
Advances in DCE-MRI Radiomics for Non-Invasive Prediction of Breast Cancer Molecular Subtypes: Research Progress and Clinical Translation.
Review in Breast cancer (Dove Medical Press), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The integration of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) with radiomics has emerged as a transformative approach for non-invasive prediction of breast cancer molecular subtypes. This review systematically evaluates methodological innovations, clinical validation milestones, and translational applications: (1) Methodological Advancements: Standardized DCE-MRI protocols combined with multidimensional radiomic features (morphological, textural, and wavelet-transformed parameters) significantly improved discriminative performance for ER, HER2, and triple-negative subtypes. (2) Deep Learning Integration: Multitask predictive models achieved early treatment response assessment and recurrence risk stratification through spatiotemporal heterogeneity analysis. (3) Clinical Validation: Prospective multicenter trials demonstrated that radiomic models showed strong concordance with 21-gene assays and could potentially replace 38% of repeat biopsies. Despite these advancements, challenges persist in data heterogeneity and mechanistic interpretation of radiomic biomarkers. Emerging strategies integrating radiogenomic analyses and organoid validation platforms are establishing new paradigms for precision imaging-guided therapy.
Indexed as
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What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.