AI Article Synopsis

  • Deep learning systems (DLSs) were developed to differentiate between follicular thyroid carcinoma (FTC) and follicular adenoma (FA) using three convolutional neural network architectures: EfficientNet, VGG16, and ResNet50.
  • The DLSs showed excellent performance with an area under the receiver operating characteristic curve of 0.91 and an F1 score of 0.82, primarily relying on nuclear features for diagnosis.
  • Additionally, the DLSs were trained to predict risk factors associated with FTC recurrence and invasions, achieving moderate accuracy, indicating potential for automated diagnosis from biopsy samples.

Article Abstract

Deep learning systems (DLSs) have been developed for the histopathological assessment of various types of tumors, but none are suitable for differential diagnosis between follicular thyroid carcinoma (FTC) and follicular adenoma (FA). Furthermore, whether DLSs can identify the malignant characteristics of thyroid tumors based only on random views of tumor tissue histology has not been evaluated. In this study, we developed DLSs able to differentiate between FTC and FA based on 3 types of convolutional neural network architecture: EfficientNet, VGG16, and ResNet50. The performance of all 3 DLSs was excellent (area under the receiver operating characteristic curve = 0.91 ± 0.04; F1 score = 0.82 ± 0.06). Visual explanations using gradient-weighted class activation mapping suggested that the diagnosis of both FTC and FA was largely dependent on nuclear features. The DLSs were then trained with FTC images and linked information (presence or absence of recurrence within 10 years, vascular invasion, and wide capsular invasion). The ability of the DLSs to diagnose these characteristics was then determined. The results showed that, based on the random views of histology, the DLSs could predict the risk of FTC recurrence, vascular invasion, and wide capsular invasion with a certain level of accuracy (area under the receiver operating characteristic curve = 0.67 ± 0.13, 0.62 ± 0.11, and 0.65 ± 0.09, respectively). Further improvement of our DLSs could lead to the establishment of automated differential diagnosis systems requiring only biopsy specimens.

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Source
http://dx.doi.org/10.1016/j.modpat.2023.100296DOI Listing

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