Prog Med Phys.  2019 Jun;30(2):39-48. 10.14316/pmp.2019.30.2.39.

Deep-Learning-Based Molecular Imaging Biomarkers: Toward Data-Driven Theranostics

Affiliations
  • 1Department of Nuclear Medicine, Seoul National University Hospital, Seoul, Korea. chy1000@gmail.com

Abstract

Deep learning has been applied to various medical data. In particular, current deep learning models exhibit remarkable performance at specific tasks, sometimes offering higher accuracy than that of experts for discriminating specific diseases from medical images. The current status of deep learning applications to molecular imaging can be divided into a few subtypes in terms of their purposes: differential diagnostic classification, enhancement of image acquisition, and image-based quantification. As functional and pathophysiologic information is key to molecular imaging, this review will emphasize the need for accurate biomarker acquisition by deep learning in molecular imaging. Furthermore, this review addresses practical issues that include clinical validation, data distribution, labeling issues, and harmonization to achieve clinically feasible deep learning models. Eventually, deep learning will enhance the role of theranostics, which aims at precision targeting of pathophysiology by maximizing molecular imaging functional information.

Keyword

Deep learning; Molecular imaging; Theranostics; Medical imaging; Imaging biomarker

MeSH Terms

Biomarkers*
Classification
Diagnostic Imaging
Learning
Molecular Imaging*
Theranostic Nanomedicine*
Biomarkers

Figure

  • Fig. 1 The output of deep learning model as a predictive biomarker. A deep convolutional neural network (CNN) model was developed to differentiate brain PET of Alzheimer's disease from healthy subjects. This model was applied to another cohort, mild cognitive impairment patients to predict future cognitive outcome. The output of the model represents a probability of Alzheimer's disease, which can be used as a predictive biomarker for predicting cognitive outcome in preclinical disorders.

  • Fig. 2 A gap between training and real-world data. Most of deep learning models are developed by patients’ data with specific disorders and controls. The problem of deep learning application to the clinic is the difference between real-world data and the training cohort. Real-world data in the clinic included heterogeneous patients different from training cohorts. Furthermore, the distribution of disease and normal is considerably different. This data distribution issue become a bigger factor when deep learning aims at general population.

  • Fig. 3 Leveraging unlabeled data as a clinical routine for facilitating deep learning development. As labeling for medical data is too expensive and time-consuming, it is a bottleneck for developing deep learning models. Since it is relatively easy to collect heterogeneous image data obtained for clinical routine, unsupervised learning can leverage these unlabeled ‘dirty’ data. Unsupervised learning-based feature extraction can be transferred to relatively small cohorts which contain both labels and images to predict clinical outcome as well as differential diagnosis according to the clinical purposes.


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