🩺 Can MRI radiomics predict pCR in breast cancer?
🩺 Can MRI radiomics predict pCR in breast cancer?
A systematic review of 35 studies in Breast Cancer found MRI radiomics models predicted pathologic complete response to neoadjuvant therapy with a pooled AUC of 0.813, but 86% of studies were underpowered and only 14% tested performance in clinically relevant subgroups. The PROSPERO-registered review suggests technical promise, but limited external validation and inconsistent demographic reporting remain major barriers to clinical use.
Why It Matters To Your Practice
pCR prediction could help clinicians better tailor neoadjuvant treatment, surgical planning, and patient counseling.
AI tools may appear accurate on paper, but weak validation and poor subgroup reporting can limit reliability at the bedside.
For clinicians evaluating new AI products, this review highlights the gap between model performance and practice readiness.
Clinical Implications
Reported model discrimination was favorable overall, but most studies were retrospective, single-center, and methodologically heterogeneous.
External validation was uncommon, so performance may drop when models are applied outside the original development setting.
Only a small minority of studies assessed subgroup performance, raising concerns about whether predictions generalize across different patient populations.
Insights
The review assessed 35 studies with sample sizes ranging from 55 to 442.
Methodological quality was evaluated with the METRICS score, and bias/fairness review was adapted from QUADAS-2.
Inconsistent reporting of demographic and clinical variables made it difficult to judge generalizability and equitable performance.
The Bottom Line
MRI radiomics for pCR prediction is promising, but not yet ready for routine clinical deployment.
Before adoption, clinicians should look for prospective multicenter validation, adequate sample size, transparent reporting, and subgroup-specific performance data.
In AI for practice, accuracy alone is not enough; trust depends on robustness, reproducibility, and fairness.