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Preoperative MRI to Predict Upstaging of DCIS to Invasive Cancer at Surgery
Sara H Javid1, Anum S Kazerouni2, Daniel S Hippe3
1Department of Surgery, University of Washington Medical Center, Seattle, WA, USA. sjavid@uw.edu.
Annals of Surgical Oncology
|January 28, 2025
Summary
Quantitative MRI features can identify ductal carcinoma in situ (DCIS) at risk of upstaging to invasive cancer. This may help avoid overtreatment and guide active surveillance for DCIS de-escalation trials.
Area of Science:
- Radiology
- Oncology
- Medical Imaging
Background:
- Ductal carcinoma in situ (DCIS) is frequently overtreated due to difficulties in predicting which cases will progress to invasive cancer.
- Core needle biopsy (CNB) diagnosis of DCIS lacks sufficient predictive power for upstaging at surgical excision.
Purpose of the Study:
- To investigate if quantitative magnetic resonance imaging (MRI) features can identify DCIS lesions diagnosed via CNB that are at risk of upstaging to invasive cancer.
- To assess the utility of quantitative MRI in guiding treatment decisions for DCIS.
Main Methods:
- Prospective observational clinical trial involving women with DCIS diagnosed by CNB.
- Quantitative analysis of dynamic contrast-enhanced (DCE) MRI features, including peak percent enhancement (PE) and Ktrans.
- Evaluation of associations between MRI features and upstaging using receiver operating characteristic (ROC) curve analysis.
Main Results:
- 15 out of 58 (26%) DCIS lesions were upstaged to invasive cancer at surgery.
- Higher peak percent enhancement (PE) on routine DCE-MRI was significantly associated with upstaging (AUC, 0.81).
- Quantitative MRI features outperformed advanced DCE-MRI metrics and other clinical/mammographic factors in predicting upstaging.
Conclusions:
- Quantitative MRI features show promise in identifying DCIS lesions likely to be upstaged to invasive cancer.
- These findings could support the selection of patients for active surveillance in de-escalation trials, potentially reducing overtreatment of DCIS.
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