Early and noninvasive prediction of response to neoadjuvant therapy for breast cancer via longitudinal ultrasound and MR deep learning: A multicentre study.

Acad Radiol

Department of Breast Surgery, Jiangxi Cancer Hospital&Institute,Jiangxi Clinical Research Center for Cancer, The Second Affiliated Hospital of Nanchang Medical College, Nanchang 330029, Jiangxi Province, China (C.H., X.Z., T.Y.). Electronic address:

Published: November 2024

Rationale And Objectives: The early prediction of response to neoadjuvant chemotherapy (NAC) will aid in the development of personalized treatments for patients with breast cancer. This study investigated the value of longitudinal multimodal deep learning (DL) based on breast MR and ultrasound (US) in predicting pathological complete response (pCR) after NAC.

Materials And Methods: We retrospectively reviewed the pre-NAC and post-2nd-NAC MR and/or US images of 448 patients enrolled from three centers and extracted DL features from the largest section of the breast tumour using ResNet50. T test, Pearson correlation analysis and least absolute shrinkage and selection operator regression were used to select the most significant DL features for the pre-NAC and post-2nd-NAC MR and US DL models. The stacking model integrates different single-modality DL models and meaningful clinical data. The diagnostic performance of the models was evaluated.

Results: In all the patients, the pCR rate was 36.65%. There was no significant difference in diagnostic performance between the different single-modality DL models (DeLong test, p > 0.05). The stacking model integrating the above four DL models with HER2 status yielded areas under the curves of 0.951-0.979, accuracies of 91.55%-92.65%, sensitivities of 90.63%-93.94%, and specificities of 89.47%-94.44% in the cohorts.

Conclusion: Longitudinal multimodal DL can be useful in predicting pCR. The stacking model can be used as a new tool for the early noninvasive prediction of the response to NAC, as evidenced by its excellent performance, and therefore aid the development of personalized treatment strategies for patients with breast cancer.

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Source
http://dx.doi.org/10.1016/j.acra.2024.10.033DOI Listing

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