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Multi-phase DCE-MRI delta-radiomics predicts Ki-67 changes in 148 breast cancer patients after neoadjuvant therapyMRI features may help predict Ki-67 changes in breast cancer after treatment

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Key Takeaway
Consider multi-phase DCE-MRI delta-radiomics for predicting Ki-67 downstaging in breast cancer after neoadjuvant therapy, though validation is needed.

This retrospective cohort study included 148 breast cancer patients who underwent surgical resection after 6–8 cycles of neoadjuvant therapy. The primary outcome was the prediction of change in Ki-67 index following neoadjuvant therapy. Three radiomics models were compared: a multi-phase DCE-MRI delta-radiomics model, a delayed-to-early delta model, and a standalone peak-phase model.

In the testing cohort, the peak-to-early delta-radiomics model demonstrated the best diagnostic performance with an AUC of 0.817 (95% CI: 0.685–0.949). The delayed-to-early delta model yielded an AUC of 0.648 (95% CI: 0.484–0.812), while the standalone peak-phase model resulted in an AUC of 0.615 (95% CI: 0.444–0.785). Both comparator models were significantly outperformed by the peak-to-early delta-radiomics model.

Significant associations were observed between HER2 status and the outcome (p = 0.031), as well as between histological grade and the outcome (p = 0.031). Adverse events, serious adverse events, discontinuations, and tolerability were not reported. The study did not report follow-up duration, funding sources, or specific limitations.

Delta-radiomics based on MRI, combined with clinical parameters, represents a promising non-invasive approach for more accurately predicting Ki-67 downstaging in breast cancer following neoadjuvant therapy, outperforming conventional radiomics models. However, because this was a retrospective cohort study, causal inferences cannot be made, and the results should be interpreted with caution pending further validation.

This study looked at 148 breast cancer patients who underwent surgery after completing six to eight cycles of neoadjuvant therapy. The goal was to see if certain MRI features could accurately predict changes in the Ki-67 index, a marker of how fast tumor cells are dividing. Scientists compared a new multi-phase MRI analysis against simpler models that used only one phase or a different timing approach.

The new multi-phase model showed the best performance, correctly identifying changes in about 82% of cases in the testing group. Other models performed less well, with accuracy rates around 62% to 65%. The researchers also found that tumor characteristics like HER2 status and histological grade were linked to the results.

Because this was a small, retrospective study, the findings are promising but not yet proven. The new MRI method is non-invasive and could help doctors plan treatment, but larger studies are needed to confirm these results. Readers should not assume this will immediately change how breast cancer is treated.

What this means for you:
A new MRI analysis may better predict tumor changes, but larger studies are needed first.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Ki-67 is a key biomarker of tumor proliferation in breast cancer. A reduction in Ki-67 following neoadjuvant therapy (NAT) reflects chemosensitivity and holds significant prognostic value. Therefore, pre-treatment assessment of Ki-67 dynamics during NAT is crucial for evaluating patient prognosis.This study aims to predict the change in Ki-67 index in breast cancer patients following NAT using radiomic features derived from DCE-MRI. This retrospective study enrolled 148 breast cancer patients who underwent surgical resection after 6–8 cycles of NAT, randomly divided into training (n=104) and test cohorts (n=44) at a 7:3 ratio. Multivariable logistic regression (P ROC curve analysis demonstrated that the peak-to-early delta-radiomics model achieved the best diagnostic performance in the testing cohort with an AUC of 0.817(95% CI: 0.685–0.949), significantly outperforming the delayed-to-early delta model [AUC = 0.648(95% CI: 0.484–0.812)]and the standalone peak-phase model [AUC = 0.615(95% CI: 0.444–0.785)]. Logistic regression analysis revealed that HER2 status (p = 0.031) and histological grade (p Delta-radiomics based on MRI, combined with clinical parameters, represents a promising non-invasive approach for more accurately predicting Ki-67 downstaging in breast cancer following NAT, outperforming conventional radiomics models. Integrating radiomic features with clinical information holds the potential to further optimize individualized treatment strategies and improve prognostic assessment for breast cancer patients.
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