Abstract

In solid tumors, elevated fluid pressure and inadequate blood perfusion resulting from unbalanced angiogenesis are the prominent reasons for the ineffective drug delivery inside tumors. To normalize the heterogeneous and tortuous tumor vessel structure, antiangiogenic treatment is an effective approach. Additionally, the combined therapy of antiangiogenic agents and chemotherapy drugs has shown promising effects on enhanced drug delivery. However, the need to find the appropriate scheduling and dosages of the combination therapy is one of the main problems in anticancer therapy. Our study aims to generate a realistic response to the treatment schedule, making it possible for future works to use these patient-specific responses to decide on the optimal starting time and dosages of cytotoxic drug treatment. Our dataset is based on our previous in-silico model with a framework for the tumor microenvironment, consisting of a tumor layer, vasculature network, interstitial fluid pressure, and drug diffusion maps. In this regard, the chemotherapy response prediction problem is discussed in the study, putting forth a proof of concept for deep learning models to capture the tumor growth and drug response behaviors simultaneously. The proposed model utilizes multiple convolutional neural network submodels to predict future tumor microenvironment maps considering the effects of ongoing treatment. Since the model has the task of predicting future tumor microenvironment maps, we use two image quality evaluation metrics, which are structural similarity and peak signal-to-noise ratio, to evaluate model performance. We track tumor cell density values of ground truth and predicted tumor microenvironments. The model predicts tumor microenvironment maps seven days ahead with the average structural similarity score of 0.973 and the average peak signal ratio of 35.41 in the test set. It also predicts tumor cell density at the end day of 7 with the mean absolute percentage error of 2.292pm 1.820.

Highlights

  • In solid tumors, elevated fluid pressure and inadequate blood perfusion resulting from unbalanced angiogenesis are the prominent reasons for the ineffective drug delivery inside tumors

  • The Diffuser-Elapser Network (DENT) model takes input tensors describing the current tumor microenvironment state, consisting of five channels, namely tumor density, vasculature, interstitial fluid pressure (IFP), antiangiogenic drug, and chemotherapy drug maps accompanied by chemotherapy and antiangiogenic drug dosages, and predicts future tumor microenvironment maps

  • structural similarity (SSIM) is mostly applied to improve or track the perceptual metrics based on the structural information; on the other hand, peak signal-to-noise ratio (PSNR) relies on estimating the pixel-wise error

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Summary

Introduction

In solid tumors, elevated fluid pressure and inadequate blood perfusion resulting from unbalanced angiogenesis are the prominent reasons for the ineffective drug delivery inside tumors. The model predicts tumor microenvironment maps seven days ahead with the average structural similarity score of 0.973 and the average peak signal ratio of 35.41 in the test set It predicts tumor cell density at the end day of 7 with the mean absolute percentage error of 2.292 ± 1.820. Due to tumor-induced angiogenesis, the newly developed vessels have a leaky and disorganized structure accompanying a microenvironment identified by hypoxia, acidosis, and increased fluid p­ ressure[2] As a result, this structurally and functionally abnormal tumor vascular network leads to heterogeneous and inadequate drug distribution inside tumors. Antiangiogenic agents maintain the balance between proangiogenic and antiangiogenic factors, similar to healthy tissues These agents normalize the structure and function of the tumor vascular network transiently by inducing reduced vessel diameter. University, Global Station for Quantum Medical Science and Engineering, Global Institution for Collaborative Research and Education (GI-CoRE), Sapporo 060‐8648, Japan. 6These authors contributed : Batuhan

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