TG468: a text graph convolutional network for predicting clinical response to immune checkpoint inhibitor therapy

Author:

Wang Kun12,Shi Jiangshan34,Tong Xiaochu34,Qu Ning34,Kong Xiangtai34,Ni Shengkun34,Xing Jing5,Li Xutong67ORCID,Zheng Mingyue12ORCID

Affiliation:

1. School of Life Sciences , Division of Life Sciences and Medicine, , Hefei 230026 , China

2. University of Science and Technology of China , Division of Life Sciences and Medicine, , Hefei 230026 , China

3. Drug Discovery and Design Center , State Key Laboratory of Drug Research, ; 555 Zuchongzhi Road, Shanghai 201203 , China

4. Shanghai Institute of Materia Medica Chinese Academy of Sciences , State Key Laboratory of Drug Research, ; 555 Zuchongzhi Road, Shanghai 201203 , China

5. Lingang Laboratory , Shanghai 200031 , China

6. Drug Discovery and Design Center , State Key Laboratory of Drug Research, , 555 Zuchongzhi Road, Shanghai 201203 , China

7. Shanghai Institute of Materia Medica, Chinese Academy of Sciences , State Key Laboratory of Drug Research, , 555 Zuchongzhi Road, Shanghai 201203 , China

Abstract

Abstract Enhancing cancer treatment efficacy remains a significant challenge in human health. Immunotherapy has witnessed considerable success in recent years as a treatment for tumors. However, due to the heterogeneity of diseases, only a fraction of patients exhibit a positive response to immune checkpoint inhibitor (ICI) therapy. Various single-gene-based biomarkers and tumor mutational burden (TMB) have been proposed for predicting clinical responses to ICI; however, their predictive ability is limited. We propose the utilization of the Text Graph Convolutional Network (GCN) method to comprehensively assess the impact of multiple genes, aiming to improve the predictive capability for ICI response. We developed TG468, a Text GCN model framing drug response prediction as a text classification task. By combining natural language processing (NLP) and graph neural network techniques, TG468 effectively handles sparse and high-dimensional exome sequencing data. As a result, TG468 can distinguish survival time for patients who received ICI therapy and outperforms single gene biomarkers, TMB and some classical machine learning models. Additionally, TG468’s prediction results facilitate the identification of immune status differences among specific patient types in the Cancer Genome Atlas dataset, providing a rationale for the model’s predictions. Our approach represents a pioneering use of a GCN model to analyze exome data in patients undergoing ICI therapy and offers inspiration for future research using NLP technology to analyze exome sequencing data.

Funder

National Natural Science Foundation of China

SIMM-SHUTCM Traditional Chinese Medicine Innovation Joint Research Program

Shanghai Municipal Science and Technology Major Project

National Key Research and Development Program of China

Publisher

Oxford University Press (OUP)

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