Comparative analysis of convolutional neural network models for the histopathological differentiation of acinic cell carcinoma and secretory carcinoma.
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Sousa-Neto Sebastião Silvério, Nakamura Thaís Cerqueira Reis, Dos Santos Giovanna Calabrese, Giraldo-Roldan Daniela, Gonçalves Moisés Willian Aparecido, de Cáceres Cinthia Verónica Bardález López, Fonseca Felipe Paiva, Moreira Victor Hugo Lopes de Oliveira, Mendonça Elismauro Francisco, Martins Manoela Domingues, Gabriel Amanda De Farias, Altemani Albina, Mariano Fernanda Viviane, Santos-Silva Alan Roger, Lopes Marcio Ajudarte, Kowalski Luiz Paulo, Araújo Anna Luíza Damaceno, Moraes Matheus Cardoso, Vargas Pablo Agustin
Аннотация
METHODS: A cross-sectional study using whole-slide images from 46 patients with acinic cell carcinoma (n = 26) or secretory carcinoma (n = 20) was conducted. Eight CNNs (ResNet-50, InceptionV3, VGG16, Xception, MobileNet, DenseNet121, EfficientNetB0, and EfficientNetV2B0) were trained and evaluated for accuracy, sensitivity, specificity, F1-score, and AUC. Performance was measured in training, validation, and test subsets. Accuracy and loss curves were also presented.
RESULTS: InceptionV3 demonstrated the best overall performance, with the lowest loss (1.39), highest accuracy (0.81), sensitivity (0.90), and F1-score (0.81). VGG16 achieved the highest AUC (0.86) and precision (0.77). DenseNet121 showed the lowest performance in terms of accuracy (0.65) and F1-Score (0.52), but the highest specificity (0.85).
CONCLUSION: This proof-of-concept study suggests that convolutional neural networks may be feasible tools to support the microscopic differentiation between acinic cell carcinoma and secretory carcinoma. The performance of these models critically depends on the size of the dataset and the quality of annotations. The findings should be interpreted cautiously given the limited dataset and potential sources of bias. Further validation with larger, multicenter datasets is needed before any clinical application can be considered.