Grant Details
| Grant Number: |
1R01CA315473-01 Interpret this number |
| Primary Investigator: |
Kann, Benjamin |
| Organization: |
Brigham And Women'S Hospital |
| Project Title: |
Clinical Characterization of Treatment-Related Morbidity in Pediatric Brain Tumor Survivors with Artificial Intelligence (Clarity-Ai) |
| Fiscal Year: |
2026 |
Abstract
Pediatric brain tumor (PBT) survivors experience chronic morbidity from their cancers and associated
treatments that have long-term negative impacts on quality of life, including physiologic frailty and accelerated
aging, characterized by sarcopenia (i.e. muscle loss). Early interventions, such as tailored exercise and
nutrition regimens can mitigate the downstream sequalae of sarcopenia, and pharmacologic therapies are
under investigation, however, the clinical issues are nuanced, variable, and difficulty characterize from clinical
data routinely collected for cancer survivors. Thus, there is an urgent need for cost-effective, practical tools to
improve early diagnosis, characterization, and monitoring of muscle status, sarcopenia, and associated
morbidity in PBT survivors. The long-term goal is to enable personalized management of PBT survivors by
identifying those at risk of sarcopenia and its downstream complications and triaging them to the appropriate
intervention. The objective of this proposal is to determine how artificial intelligence (AI) algorithms applied to
routine, clinical imaging can diagnose sarcopenia and predict morbidity in PBT survivors. The central
hypothesis is that AI innovations developed by our group can be successfully applied to children, adolescents,
and young adult survivors of brain cancers to characterize and predict morbidity in survivorship. Our
hypothesis makes specific predictions that we will test by applying AI tools developed within our group to large,
multi-institutional cohorts, including one retrospective and two prospective cohorts of PBT survivors (2,649
patients with detailed clinical and outcomes data and ~20,000 longitudinal magnetic resonance images (MRIs).
We will study the following aims: 1) identify and characterize risk factors associated with sarcopenia diagnosed
from AI-based temporalis muscle thickness; 2) test the hypothesis that AI-based temporalis muscle thickness
(iTMT) can characterize and predict morbidity (physiologic frailty, neurocognitive and endocrine dysfunction)
and mortality in PBT survivors; and 3) evaluate a 3-dimensional extracranial tissue assessment tool that
includes temporalis muscle volume measurement and determine if volumetric muscle assessment improves
outcome prediction in PBT survivors. The expected outcome of this work is the development of publicly
available, cost-effective AI tools that effectively diagnosis sarcopenia and provide an early indicator of
associated morbidity in pediatric cancer survivors. The results will have an immediate positive impact as they
will establish a better understanding of sarcopenia and related morbidity in cancer survivorship and ultimately
enable inexpensive, practical, automated diagnosis and tracking of sarcopenia across patients with cancer and
other diseases.
Publications
None