We demonstrate statistical relationships between routine multiparametric imaging signatures and underlying cellular and molecular properties of brain tumors. We apply advanced statistical methods to correct for the family-wise error rate problem associated with whole-brain statistical parametric mapping, and show that the results have strong agreement with surgical biopsy. These results imply that cellular and molecular mapping of tumor heterogeneity from minimally-invasive images may be possible in the near future.
This abstract and the presentation materials are available to members only; a login is required.