AI predicts pediatric glioma recurrence using multiple brain scans

Artificial intelligence (AI) shows tremendous promise for analyzing vast medical imaging datasets and identifying patterns that may be missed by human observers. AI-assisted interpretation of brain scans may help improve care for children with brain tumors called gliomas, which are typically treatable but vary in risk of recurrence. Investigators from Mass General Brigham and collaborators at Boston Children's Hospital and Dana-Farber/Boston Children's Cancer and Blood Disorders Center trained deep learning algorithms to analyze sequential, post-treatment brain scans and flag patients at risk of cancer recurrence. Their results are published in The New England Journal of Medicine AI

Many pediatric gliomas are curable with surgery alone, but when relapses occur, they can be devastating. It is very difficult to predict who may be at risk of recurrence, so patients undergo frequent follow-up with magnetic resonance (MR) imaging for many years, a process that can be stressful and burdensome for children and families. We need better tools to identify early which patients are at the highest risk of recurrence." 

Benjamin Kann, MD, corresponding author of the Artificial Intelligence in Medicine (AIM) Program at Mass General Brigham and the Department of Radiation Oncology at Brigham and Women's Hospital

Studies of relatively rare diseases, like pediatric cancers, can be challenged by limited data. This study, which was funded in part by the National Institutes of Health, leveraged institutional partnerships across the country to collect nearly 4,000 MR scans from 715 pediatric patients. To maximize what AI could "learn" from a patient's brain scans - and more accurately predict recurrence - the researchers employed a technique called temporal learning, which trains the model to synthesize findings from multiple brain scans taken over the course of several months post-surgery. 

Typically, AI models for medical imaging are trained to draw conclusions from single scans; with temporal learning, which has not previously been used for medical imaging AI research, images acquired over time inform the algorithm's prediction of cancer recurrence. To develop the temporal learning model, the researchers first trained the model to sequence a patient's post-surgery MR scans in chronological order so that the model could learn to recognize subtle changes. From there, the researchers fine-tuned the model to correctly associate changes with subsequent cancer recurrence, where appropriate. 

Ultimately, the researchers found that the temporal learning model predicted recurrence of either low- or high-grade glioma by one-year post-treatment, with an accuracy of 75-89 percent - substantially better than the accuracy associated with predictions based on single images, which they found to be roughly 50 percent (no better than chance). Providing the AI with images from more timepoints post-treatment increased the model's prediction accuracy, but only four to six images were required before this improvement plateaued. 

The researchers caution that further validation across additional settings is necessary prior to clinical application. Ultimately, they hope to launch clinical trials to see if AI-informed risk predictions can result in improvements to care - whether by reducing imaging frequency for the lowest-risk patients or by preemptively treating high-risk patients with targeted adjuvant therapies. 

"We have shown that AI is capable of effectively analyzing and making predictions from multiple images, not just single scans," said first author Divyanshu Tak, MS, of the AIM Program at Mass General Brigham and the Department of Radiation Oncology at the Brigham. "This technique may be applied in many settings where patients get serial, longitudinal imaging, and we're excited to see what this project will inspire." 

Source:
Journal reference:

Tak, D., et al. (2025) Longitudinal Risk Prediction for Pediatric Glioma with Temporal Deep Learning. NEJM AI. doi.org/10.1056/AIoa2400703.

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