Abstract
Objectives
This study was conducted in order to investigate whether there is a correlation between the time-to-enhancement (TTE) in ultrafast MRI and histopathological characteristics of breast cancers.
Methods
Between January and August 2017, 274 consecutive breast cancer patients (mean age, 53.5 years; range, 25–80 years) who underwent ultrafast MRI and subsequent surgery were included for analysis. Ultrafast MRI scans were acquired using TWIST-VIBE or 4D TRAK-3D TFE sequences. TTE and maximum slope (MS) were derived from the ultrafast MRI. The repeated measures ANOVA, Mann–Whitney U test and Kruskal–Wallis H test were performed to compare the median TTE, MS and SER according to histologic type, histologic grade, ER/PR/HER2 positivity, level of Ki-67 and tumour subtype. For TTE calculation, intraclass correlation coefficient (ICC) was used to evaluate interobserver variability.
Results
The median TTE of invasive cancers was shorter than that of in situ cancers (p < 0.001). In invasive cancers, large tumours showed shorter TTE than small tumours (p = 0.001). High histologic/nuclear grade cancers had shorter TTE than low to intermediate grade cancers (p < 0.001 and p < 0.001). HER2-positive cancers showed shorter TTE than HER2-negative cancers (p = 0.001). The median TTE of cancers with high Ki-67 was shorter than that of cancers with low Ki-67 (p < 0.001). ICC between two readers showed moderate agreement (0.516). No difference was found in the median MS or SER values according to the clinicopathologic features.
Conclusions
The median TTE of breast cancer in ultrafast MRI was shorter in invasive or aggressive tumours than in in situ cancer or less aggressive tumours, respectively.
Key Points
• Invasive breast tumours show a shorter TTE in ultrafast DCE-MRI than in situ cancers.
• A shorter TTE in ultrafast DCE-MRI is associated with breast tumours of a large size, high histologic or nuclear grade, PR negativity, HER2 positivity and high Ki-67 level.
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Abbreviations
- DCE:
-
Dynamic contrast-enhanced
- ER:
-
Oestrogen receptor
- eTHRIVE:
-
Enhanced T1-weighted high-resolution isotropic volume examination
- HER2:
-
Human epidermal growth factor receptor (HER)-2
- IHC:
-
Immunohistochemistry
- MRI:
-
Magnetic resonance imaging
- MS:
-
Maximum slope
- PR:
-
Progesterone receptor
- ROI:
-
Region of interest
- SER:
-
Signal enhancement ratio
- TFE:
-
Turbo field echo
- TRAK:
-
Time-resolved MR angiography with keyhole
- TTE:
-
Time-to-enhancement
- TWIST:
-
Time-resolved angiography with interleaved stochastic trajectories
- VIBE:
-
Volume-interpolated breath-hold examination
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Funding
This study has received funding by a grant (no. 04-2017-0470) from the Seoul National University Hospital Research Fund.
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The scientific guarantor of this publication is Nariya Cho MD, PhD, Professor of the Department of Radiology, Seoul National University Hospital.
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Shin, S.U., Cho, N., Kim, SY. et al. Time-to-enhancement at ultrafast breast DCE-MRI: potential imaging biomarker of tumour aggressiveness. Eur Radiol 30, 4058–4068 (2020). https://doi.org/10.1007/s00330-020-06693-0
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DOI: https://doi.org/10.1007/s00330-020-06693-0