Abstract

BackgroundLung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Currently, accurate staging is a prerequisite for effective diagnosis and treatment of lung adenocarcinoma. Previous research has used mainly single-modal data, such as gene expression data, for classification and prediction. Integrating multi-modal genetic data (gene expression RNA-seq, methylation data and copy number variation) from the same patient provides the possibility of using multi-modal genetic data for cancer prediction. A new machine learning method called gcForest has recently been proposed. This method has been proven to be suitable for classification in some fields. However, the model may face challenges when applied to small samples and high-dimensional genetic data.ResultsIn this paper, we propose a multi-weighted gcForest algorithm (MLW-gcForest) to construct a lung adenocarcinoma staging model using multi-modal genetic data. The new algorithm is based on the standard gcForest algorithm. First, different weights are assigned to different random forests according to the classification performance of these forests in the standard gcForest model. Second, because the feature vectors generated under different scanning granularities have a diverse influence on the final classification result, the feature vectors are given weights according to the proposed sorting optimization algorithm. Then, we train three MLW-gcForest models based on three single-modal datasets (gene expression RNA-seq, methylation data, and copy number variation) and then perform decision fusion to stage lung adenocarcinoma. Experimental results suggest that the MLW-gcForest model is superior to the standard gcForest model in constructing a staging model of lung adenocarcinoma and is better than the traditional classification methods. The accuracy, precision, recall, and AUC reached 0.908, 0.896, 0.882, and 0.96, respectively.ConclusionsThe MLW-gcForest model has great potential in lung adenocarcinoma staging, which is helpful for the diagnosis and personalized treatment of lung adenocarcinoma. The results suggest that the MLW-gcForest algorithm is effective on multi-modal genetic data, which consist of small samples and are high dimensional.

Highlights

  • Lung cancer is one of the most common cancers and possesses the highest morbidity and mortality, causing more than 1.4 million deaths each year

  • (1) we set dynamic weights for different random forests in the multi-grained scanning according to the classification performance of each random forest; (2) we propose a sorting optimization algorithm to set different weights for each sliding window, as the class vectors generated by each sliding window have varying effects on the final prediction results; and (3) we adopt decision-level fusion to construct a staging model of lung adenocarcinoma based on multi-modal genetic data

  • Materials To evaluate the performance of the MLW-gcForest algorithm, methylation data, RNA-seq data, copy number variation (CNV) data and corresponding clinical data of lung adenocarcinoma are downloaded from the the Cancer Genome Atlas (TCGA) [37]

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Summary

Introduction

Lung cancer is one of the most common cancers and possesses the highest morbidity and mortality, causing more than 1.4 million deaths each year. The 5-year survival rate of lung adenocarcinoma does not exceed 5% [3]. Different treatments are needed during different stages of lung adenocarcinoma to improve the patient’s survival rate. The accurate staging of lung adenocarcinoma is the first step in clinical diagnosis and targeted treatment. Lung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Accurate staging is a prerequisite for effective diagnosis and treatment of lung adenocarcinoma. A new machine learning method called gcForest has recently been proposed. This method has been proven to be suitable for classification in some fields. The model may face challenges when applied to small samples and high-dimensional genetic data

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