Baseline MRI BI-RADS and breast oedema score features as predictors for axillary lymph node response to neoadjuvant chemotherapy in breast cancer
Author Block: C. Malhaire1, O. Umay1, F. Frouin2; 1Paris/FR, 2Orsay/FR
Purpose: The aim of this study was to assess the association between pre-treatment breast MRI features and axillary lymph node residual disease in women treated for node-positive breast cancer by neoadjuvant chemotherapy (NAC).
Methods or Background: In this single-centre, retrospective study, women with node-positive breast cancer who underwent NAC and pre-treatment breast MRI between 2016 and 2021 were included. MRIs were evaluated using the standardised BI-RADS and T2-weighted Breast Oedema Score. Univariate analysis and multivariate logistic regression analysis were conducted to evaluate clinicopathological and MRI variables association with lymph node residual disease. A prediction model was developed from the logistic regression analysis and evaluated on a randomly split train and test set (7:3 ratio).
Results or Findings: Of 142 breast cancers, 59% achieved post-NAC nodal response, varying by subtype: luminal 24%, HER2+ 69%, and TN 75%. Factors associated with nodal response were TN and HER2+ subtypes, high Ki67, and tumour-infiltrating lymphocytes. Univariate analysis identified MRI features like anterior third location, indicating the depth of the tumour within the breast, and irregular shape as significant for residual axillary disease. In multivariate analysis, the anterior location and the absence of intratumoural T2 hyperintensity remained significant. Adding MRI features to anatomopathological variables enhanced nodal residual disease prediction models.
Conclusion: Luminal subtypes, low Ki67 levels, anterior third location, and lack of intratumoural T2 hyperintensity are independently associated with axillary residual disease and provide additional predictive value to predict lymph node residual disease after NAC
Limitations: Study limitations include a single-centre design, a retrospective nature, and a limited sample size for histomolecular subtype subgroup analysis.
Funding for this study: No funding was received.
Has your study been approved by an ethics committee? Yes
Ethics committee - additional information: This study was approved by the relevant Institutional Reveiw Board.