Objectives: To evaluate the performance of semi-quantitative analysis versus quantitative pharmacokinetic analysis applied to ultrafast dynamic contrast-enhanced (UF-DCE) MRI in: (1) differentiating benign from malignant breast lesions, (2) molecular subtyping, and (3) predicting pathologic complete response (pCR) following neoadjuvant chemotherapy.
Materials and methods: This prospective noninferiority study enrolled 339 consecutive participants with suspected breast lesions between September 2022 and February 2024. All underwent breast DCE MRI with a temporal resolution of 4.5 s, totaling 100 phases. Using the initial 30 phases (early-phase UF-DCE), five semi-quantitative parameters were calculated: wash-in slope (WIS), time-to-peak, bolus arrival time, peak enhancement intensity (PEI), and initial area under the curve in 60 s. Furthermore, three quantitative parameters: volume transfer constant, rate constant (kep), and extravascular extracellular space volume, were derived from the 100-phase dataset (full time-course UF-DCE). Diagnostic performance was assessed using areas under the curve (AUC) and the DeLong test, with Pearson analysis evaluating the correlation between semi-quantitative and quantitative parameters.
Results: All semi-quantitative and quantitative parameters showed differences between benign and malignant breast lesions (p < 0.001). Semi-quantitative WIS demonstrated noninferior diagnostic performance to quantitative kep in differentiating benign from malignant lesions (AUC: 0.93 vs 0.92; ∆AUC = 0.02, p = 0.35). However, neither approach effectively distinguished molecular subtypes or predicted pCR (p > 0.05). Strong correlations were observed in PEI and Ktrans (r = 0.75, p < 0.001).
Conclusion: Semi-quantitative analysis of early-phase UF-DCE exhibits noninferior performance to quantitative analysis of full time-course UF-DCE MRI for distinguishing benign from malignant breast lesions. Both analytical approaches showed limited utility in molecular subtyping and pCR prediction.
Critical relevance statement: Early-phase UF-DCE MRI provides a cost-effective alternative to full time-course UF-DCE MRI for differentiating benign and malignant breast lesions, demonstrating noninferior diagnostic performance with reduced scan time and no need for pharmacokinetic modeling.
Key points: Systematic comparison of early-phase UF-DCE and full time-course UF-DCE MRI for diagnosis, subtyping, and response prediction in a single breast cancer cohort remains limited. Early-phase UF-DCE MRI demonstrated noninferior diagnostic performance to full time-course UF-DCE MRI in differentiating benign and malignant breast lesions. Early-phase UF-DCE MRI is a time-efficient alternative to full time-course UF-DCE MRI for clinical implementation.
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