{"title":"A twin-tower model using MRI and gene for prediction on brain tumor patients' response to therapy.","authors":"Qiyuan Lyu, Fumie Costen","doi":"10.1093/bioadv/vbaf041","DOIUrl":null,"url":null,"abstract":"<p><strong>Motivation: </strong>Glioma is the most prevalent and aggressive primary brain tumor, with a poor prognosis of patients and a high mortality rate. Standard treatment of surgery, radiation, and chemotherapy may not be effective for some patients as they suffer from a stable progression of disease after treatment. Hence, it is crucial to predict the patient's response to therapy as a guide for the treatment plan. In this paper, we propose a multimodal model based on both magnetic resonance imaging and genomic data. As the dataset has a majority of single-modality samples with a few ratios of multi-modality samples, we propose a twin-tower architecture to solve the unimodal dominance issue and fully use the single-modality data.</p><p><strong>Results: </strong>The proposed architecture comprises an image encoder and a gene encoder trained on the single-modality samples for feature extraction, along with a classification head trained on multi-modality samples. In this way, all the single-modality samples can be beneficial to the whole model, and the need for the multi-modality is diminished. The proposed model outperforms the comparison methods across all metrics, achieving an accuracy of 85% on the cross-validation. The ablation experiment comparing the proposed architecture with single-modality models reflects the effectiveness of the proposed twin-tower architecture.</p><p><strong>Availability and implementation: </strong>The proposed model exhibits excellent scalability and can accommodate the integration of additional modalities without the requirement of too many multi-modality samples.</p>","PeriodicalId":72368,"journal":{"name":"Bioinformatics advances","volume":"5 1","pages":"vbaf041"},"PeriodicalIF":2.4000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12070387/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioinformatics advances","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/bioadv/vbaf041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Motivation: Glioma is the most prevalent and aggressive primary brain tumor, with a poor prognosis of patients and a high mortality rate. Standard treatment of surgery, radiation, and chemotherapy may not be effective for some patients as they suffer from a stable progression of disease after treatment. Hence, it is crucial to predict the patient's response to therapy as a guide for the treatment plan. In this paper, we propose a multimodal model based on both magnetic resonance imaging and genomic data. As the dataset has a majority of single-modality samples with a few ratios of multi-modality samples, we propose a twin-tower architecture to solve the unimodal dominance issue and fully use the single-modality data.
Results: The proposed architecture comprises an image encoder and a gene encoder trained on the single-modality samples for feature extraction, along with a classification head trained on multi-modality samples. In this way, all the single-modality samples can be beneficial to the whole model, and the need for the multi-modality is diminished. The proposed model outperforms the comparison methods across all metrics, achieving an accuracy of 85% on the cross-validation. The ablation experiment comparing the proposed architecture with single-modality models reflects the effectiveness of the proposed twin-tower architecture.
Availability and implementation: The proposed model exhibits excellent scalability and can accommodate the integration of additional modalities without the requirement of too many multi-modality samples.