# Convolutional Invasion and Expansion Networks for Tumor Growth Prediction

arXiv: https://arxiv.org/abs/1801.08468 · HTML: https://mlsanity.com/paper/1801.08468/

## Key facts

- Cited by 6 papers in the map (data through 14 Oct 2026).
- First posted on arXiv 25 Jan 2018.

## Built on by (most cited first, 6 of 6)

- [Treatment-aware Diffusion Probabilistic Model for Longitudinal MRI Generation and Diffuse Glioma Growth Prediction](https://mlsanity.com/paper/2309.05406/) (2023)
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- [Attention-based Multi-scale Gated Recurrent Encoder with Novel Correlation Loss for COVID-19 Progression Prediction](https://mlsanity.com/paper/2107.08330/) (2021)
- [An Uncertainty-aware Hierarchical Probabilistic Network for Early Prediction, Quantification and Segmentation of Pulmonary Tumour Growth](https://mlsanity.com/paper/2104.08789/) (2021)
- [Deformation Driven Seq2Seq Longitudinal Tumor and Organs-at-Risk Prediction for Radiotherapy](https://mlsanity.com/paper/2106.09076/) (2021)
- [Prediction of brain tumor recurrence location based on multi-modal fusion and nonlinear correlation learning](https://mlsanity.com/paper/2304.13725/) (2023)

## Abstract (arXiv)

Tumor growth is associated with cell invasion and mass-effect, which are traditionally formulated by mathematical models, namely reaction-diffusion equations and biomechanics. Such models can be personalized based on clinical measurements to build the predictive models for tumor growth. In this paper, we investigate the possibility of using deep convolutional neural networks (ConvNets) to directly represent and learn the cell invasion and mass-effect, and to predict the subsequent involvement regions of a tumor. The invasion network learns the cell invasion from information related to metabolic rate, cell density and tumor boundary derived from multimodal imaging data. The expansion network models the mass-effect from the growing motion of tumor mass. We also study different architectures that fuse the invasion and expansion networks, in order to exploit the inherent correlations among them. Our network can easily be trained on population data and personalized to a target patient, unlike most previous mathematical modeling methods that fail to incorporate population data. Quantitative experiments on a pancreatic tumor data set show that the proposed method substantially outperforms a state-of-the-art mathematical model-based approach in both accuracy and efficiency, and that the information captured by each of the two subnetworks are complementary.
