Abstract
Classification of benign and malignant in lung nodules using chest CT images is a key step in the diagnosis of early-stage lung cancer, as well as an effective way to improve the patients’ survival rate. However, due to the diversity of lung nodules and the visual similarity of lung nodules to their surrounding tissues, it is difficult to construct a robust classification model with conventional deep learning–based diagnostic methods. To address this problem, we propose a multi-model ensemble learning architecture based on 3D convolutional neural network (MMEL-3DCNN). This approach incorporates three key ideas: (1) Constructed multi-model network architecture can be well adapted to the heterogeneity of lung nodules. (2) The input that concatenated of the intensity image corresponding to the nodule mask, the original image, and the enhanced image corresponding to which can help training model to extract advanced feature with more discriminative capacity. (3) Select the corresponding model to different nodule size dynamically for prediction, which can improve the generalization ability of the model effectively. In addition, ensemble learning is applied in this paper to further improve the robustness of the nodule classification model. The proposed method has been experimentally verified on the public dataset, LIDC-IDRI. The experimental results show that the proposed MMEL-3DCNN architecture can obtain satisfactory classification results.
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Acknowledgments
The authors acknowledge the National Cancer Institute and the Foundation for the National Institutes of Health and their critical role in the creation of the free publicly available LIDC-IDRI Database used in this study.
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The National Key R&D Program of China (Grant No. 2017YFC0112804) supported this work.
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Liu, H., Cao, H., Song, E. et al. Multi-model Ensemble Learning Architecture Based on 3D CNN for Lung Nodule Malignancy Suspiciousness Classification. J Digit Imaging 33, 1242–1256 (2020). https://doi.org/10.1007/s10278-020-00372-8
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DOI: https://doi.org/10.1007/s10278-020-00372-8