AI Article Synopsis

  • The study focuses on developing a multimodal fusion radiomics (MFR) model to assess chemosensitivity in young high-risk low-grade gliomas (HRLGGs), which is crucial for guiding treatment decisions after surgery.
  • The MFR model combines data from macroscopic MRI and microscopic pathological images, using an attention mechanism to predict how well patients will respond to temozolomide (TMZ) based on tumor characteristics.
  • Results show that the MFR model has excellent predictive accuracy, outperforming traditional molecular markers and effectively identifying patients who are most likely to benefit from postoperative chemotherapy.

Article Abstract

Objectives: As a few types of glioma, young high-risk low-grade gliomas (HRLGGs) have higher requirements for postoperative quality of life. Although adjuvant chemotherapy with delayed radiotherapy is the first treatment strategy for HRLGGs, not all HRLGGs benefit from it. Accurate assessment of chemosensitivity in HRLGGs is vital for making treatment choices. This study developed a multimodal fusion radiomics (MFR) model to support radiochemotherapy decision-making for HRLGGs.

Methods: A MFR model combining macroscopic MRI and microscopic pathological images was proposed. Multiscale features including macroscopic tumor structure and microscopic histological layer and nuclear information were grabbed by unique paradigm, respectively. Then, these features were adaptively incorporated into the MFR model through attention mechanism to predict the chemosensitivity of temozolomide (TMZ) by means of objective response rate and progression free survival (PFS).

Results: Macroscopic tumor texture complexity and microscopic nuclear size showed significant statistical differences (p < 0.001) between sensitivity and insensitivity groups. The MFR model achieved stable prediction results, with an area under the curve of 0.950 (95% CI: 0.942-0.958), sensitivity of 0.833 (95% CI: 0.780-0.848), specificity of 0.929 (95% CI: 0.914-0.936), positive predictive value of 0.833 (95% CI: 0.811-0.860), and negative predictive value of 0.929 (95% CI: 0.914-0.934). The predictive efficacy of MFR was significantly higher than that of the reported molecular markers (p < 0.001). MFR was also demonstrated to be a predictor of PFS.

Conclusions: A MFR model including radiomics and pathological features predicts accurately the response postoperative TMZ treatment.

Clinical Relevance Statement: Our MFR model could identify young high-risk low-grade glioma patients who can have the most benefit from postoperative upfront temozolomide (TMZ) treatment.

Key Points: • Multimodal radiomics is proposed to support the radiochemotherapy of glioma. • Some macro and micro image markers related to tumor chemotherapy sensitivity are revealed. • The proposed model surpasses reported molecular markers, with a promising area under the curve (AUC) of 0.95.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00330-023-10378-9DOI Listing

Publication Analysis

Top Keywords

mfr model
12
radiochemotherapy decision-making
8
young high-risk
8
high-risk low-grade
8
macroscopic tumor
8
study radiochemotherapy
4
decision-making young
4
low-grade glioma
4
glioma patients
4
macroscopic
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!