Deep Learning of Multimodal Ultrasound: Stratifying the Response to Neoadjuvant Chemotherapy in Breast Cancer Before Treatment

Author:

Gu Jionghui12,Zhong Xian23,Fang Chengyu1,Lou Wenjing1,Fu Peifen4,Woodruff Henry C25,Wang Baohua1,Jiang Tianan1ORCID,Lambin Philippe25

Affiliation:

1. Department of Ultrasound, The First Affiliated Hospital, College of Medicine, Zhejiang University , Hangzhou , People’s Republic of China

2. The D-Lab, Department of Precision Medicine, GROW - School for Oncology and Reproduction, Maastricht University , Maastricht , The Netherlands

3. Department of Ultrasound, The First Affiliated Hospital of Sun Yat-Sen University , Guangzhou , People’s Republic of China

4. Department of Breast Surgery, The First Affiliated Hospital, School of Medicine, Zhejiang University , Hangzhou, Zhejiang , People’s Republic of China

5. Department of Radiology and Nuclear Medicine, GROW - School for Oncology and Reproduction, Maastricht University Medical Centre , Maastricht , The Netherlands

Abstract

Abstract Background Not only should resistance to neoadjuvant chemotherapy (NAC) be considered in patients with breast cancer but also the possibility of achieving a pathologic complete response (PCR) after NAC. Our study aims to develop 2 multimodal ultrasound deep learning (DL) models to noninvasively predict resistance and PCR to NAC before treatment. Methods From January 2017 to July 2022, a total of 170 patients with breast cancer were prospectively enrolled. All patients underwent multimodal ultrasound examination (grayscale 2D ultrasound and ultrasound elastography) before NAC. We combined clinicopathological information to develop 2 DL models, DL_Clinical_resistance and DL_Clinical_PCR, for predicting resistance and PCR to NAC, respectively. In addition, these 2 models were combined to stratify the prediction of response to NAC. Results In the test cohort, DL_Clinical_resistance had an AUC of 0.911 (95%CI, 0.814-0.979) with a sensitivity of 0.905 (95%CI, 0.765-1.000) and an NPV of 0.882 (95%CI, 0.708-1.000). Meanwhile, DL_Clinical_PCR achieved an AUC of 0.880 (95%CI, 0.751-0.973) and sensitivity and NPV of 0.875 (95%CI, 0.688-1.000) and 0.895 (95%CI, 0.739-1.000), respectively. By combining DL_Clinical_resistance and DL_Clinical_PCR, 37.1% of patients with resistance and 25.7% of patients with PCR were successfully identified by the combined model, suggesting that these patients could benefit by an early change of treatment strategy or by implementing an organ preservation strategy after NAC. Conclusions The proposed DL_Clinical_resistance and DL_Clinical_PCR models and combined strategy have the potential to predict resistance and PCR to NAC before treatment and allow stratified prediction of NAC response.

Funder

CHAIMELEON

EuCanImage

IMI-OPTIMA

AIDAVA

REALM

EUCAIM

China Scholarships Council

Scientific Research Fund of Zhejiang Provincial Education Department

National Major Scientific Research Instrument

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference37 articles.

1. Neoadjuvant treatment of breast cancer;Thompson,2012

2. Neoadjuvant chemotherapy in breast cancer: more than just downsizing;Derks,2018

3. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis;Cortazar,2014

4. Long-term prognostic risk after neoadjuvant chemotherapy associated with residual cancer burden and breast cancer subtype;Symmans,2017

5. Response rates and pathologic complete response by breast cancer molecular subtype following neoadjuvant chemotherapy;Haque,2018

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