Predicting Response of Triple-Negative Breast Cancer to Neoadjuvant Chemotherapy Using a Deep Convolutional Neural Network–Based Artificial Intelligence Tool

Author:

Krishnamurthy Savitri1ORCID,Jain Parag2,Tripathy Debu1ORCID,Basset Roland1ORCID,Randhawa Ramandeep2,Muhammad Hassan2,Huang Wei2ORCID,Yang Hua2,Kummar Shivaani3ORCID,Wilding George2,Roy Rajat2

Affiliation:

1. University of Texas MD Anderson Cancer Center, Houston, TX

2. PathomIQ Inc, Cupertini, CA

3. Oregon Health Science University, Portland, OR

Abstract

PURPOSE Achieving a pathological complete response (pCR) to neoadjuvant chemotherapy (NAC) is associated with improved patient outcomes in triple-negative breast cancer (TNBC). Currently, there are no validated predictive biomarkers for the response to NAC in TNBC. We developed and validated a deep convolutional neural network–based artificial intelligence (AI) model to predict the response of TNBC to NAC. MATERIALS AND METHODS Whole-slide images (WSIs) of hematoxylin and eosin–stained core biopsies from 165 (pCR in 60 and non-pCR in 105) and 78 (pCR in 31 and non-pCR in 47) patients with TNBC were used to train and validate the model. The model extracts morphometric features from WSIs in an unsupervised manner, thereby generating clusters of morphologically similar patterns. Downstream ranking of clusters provided regions of interest and morphometric scores; a low score close to zero and a high score close to one represented a high or low probability of response to NAC. RESULTS The predictive ability of AI score for the entire cohort of 78 patients with TNBC ascertained by receiver operating characteristic analysis demonstrated an area under the curve (AUC) of 0.75. The AUC for stages I, II, and III disease were 0.88, 0.73, and 0.74, respectively. Using a cutoff value of 0.35, the positive predictive value of the AI score for pCR was 73.7%, and the negative predictive value was 76.2% for non-pCR patients. CONCLUSION To our knowledge, this study is the first to demonstrate the use of an AI tool on digitized hematoxylin and eosin–stained tissue images to predict the response to NAC in patients with TNBC with high accuracy. If validated in subsequent studies, these results may serve as an ancillary aid for individualized therapeutic decisions in patients with TNBC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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