Peritumoral Radiomics

Peritumoral radiomics is an imaging-based approach that quantifies patterns in tissue surrounding a tumor to characterize the cancer microenvironment and improve interpretation beyond the visible tumor boundary. By segmenting a lesion on CT, MRI, or PET and analyzing a defined peritumoral region, researchers extract features such as signal intensity, texture, shape, and spatial heterogeneity, which can relate to invasion, angiogenesis, or treatment response. In cancer research, these measurements support risk stratification, diagnosis, prognosis, and prediction of therapy response, while integrating peritumoral information may reveal biological characteristics that conventional tumor-only analysis misses.

Peritumoral Radiomics - Related Videos

Research

JoVE Journal - Engineering

Guidelines and Experience Using Imaging Biomarker Explorer (IBEX) for Radiomics

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Cited by 28 •

2018

We describe IBEX, an open-source tool designed for medical imaging radiomics studies, and how to use this tool. In addition, some published works that have used IBEX for uncertainty analysis and model building are showcased.

Enhancing Drug Delivery in Recurrent Glioblastoma with Laser-Induced Hyperthermia

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2025

Begin with an anesthetized human patient diagnosed with recurrent glioblastoma, an invasive tumor characterized by tumor cell infiltration into the surrounding peritumoral region.The peritumoral region retains an intact blood-brain barrier (BBB), where tight junctions between endothelial cells restrict drug penetration.Make an incision in the scalp, create an opening in the skull, and insert a laser probe into the tumor core using MRI guidance.Deliver laser light through the probe.Tissue...

Invasive Behavior of Human Breast Cancer Cells in Embryonic Zebrafish

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Cited by 44 •

2017

Here, we describe xenograft zebrafish models using two different injection sites, i.e., perivitelline space and duct of Cuvier, to investigate the invasive behavior and to assess the intravasation and extravasation potential of human breast cancer cells, respectively.

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