Background
The axillary lymph node status is critical for breast cancer staging and individualized treatment planning.
Purpose
To assess the effect of determining axillary lymph node (ALN) metastasis by breast MRIâderived radiomic signatures, and compare the discriminating abilities of different MR sequences.
Study Type
Retrospective.
Population
In all, 120 breast cancer patients, 59 with ALN metastasis and 61 without metastasis, all confirmed by pathology.
Field Strength/Sequence
3 .0T scanner with T1âweighted imaging, T2âweighted imaging, diffusionâweighted imaging, and dynamic contrastâenhanced (DCE) sequences.
Assessment
Typical morphological and texture features of the segmented tumor were extracted from four sequences, ie, T1WI, T2WI, DWI, and the second postcontrast phase (CE2) of the dynamic contrastâenhanced sequences. Additional contrast enhancement kinetic features were extracted from all DCE sequences (one preâ and seven postcontrast phases). Linear discriminant analysis classifiers were built and compared when using features from an individual sequence or the combination of the sequences in differentiating the ALN metastasis status.
Statistical Tests
MannâWhitney Uâtest, Fisher's exact test, least absolute shrinkage selection operator (LASSO) regression, and receiver operating characteristic analysis were performed.
Results
The accuracy/AUC of the four sequences was 79%/0.87, 77%/0.85, 74%/0.79, and 79%/0.85 for the T1WI, CE2, T2WI, and DWI, respectively. When CE2 was augmented by adding kinetic features, the model achieved the highest performance (accuracyâ=â0.86 and AUCâ=â0.91). When all features from the four sequences and the kinetics were combined, it did not lead to a further increase in the performance (Pâ=â0.48).
Data Conclusion
Breast tumor's radiomic signatures from preoperative breast MRI sequences are associated with the ALN metastasis status, where CE2 phase and the contrast enhancement kinetic features lead to the highest classification effect.
Level of Evidence 3
Technical Efficacy Stage 2
J. Magn. Reson. Imaging 2019;50:1125â1132.