Abstract 694: Spatially resolved genomics reveals evolutionary modes and imaging correlates in glioblastoma.

Abstract The spatial evolutionary dynamics of glioblastoma remain poorly understood. Here, we performed spatially resolved molecular profiling of 78 multi-regional tumor specimens from 24 GBM patients by integrating neuro-navigation-guided intraoperative sampling with deep whole-exome sequencing. This dataset represents one of the most spatially detailed genomic resources for GBM to date. By coupling spatial coordinates with genomic complexity, we delineated two distinct evolutionary trajectories: an “Expansive” model, in which three-dimensional growth and molecular diversification proceed in parallel, and a “Stochastic” model, where genomic diversification occurs independently of spatial expansion. These models were supported by phylogenetic reconstruction and radiogenomic analyses, revealing how spatial architecture constrains clonal dynamics. Quantitative integration of molecular and physical distances uncovered that tumors with greater spatially correlated genomic diversity exhibited worse clinical outcomes. Patients harboring “Stochastic” tumors demonstrated inferior survival probabilities compared to those with “Expansive” tumors, suggesting that spatially derived molecular metrics may serve as prognostic indicators of tumor aggressiveness. Furthermore, MRI-derived radiomic features, particularly texture-based metrics from T1-contrast enhanced images, mirrored underlying genomic complexity and aligned with evolutionary modes, establishing a link between intratumoral heterogeneity and noninvasive imaging phenotypes. While prior genomic studies have characterized GBM evolution at the molecular level, most lacked spatial resolution and failed to capture the three-dimensional architecture of tumor growth within the human brain. Our study overcomes this limitation through an international collaboration between the Medical University of Innsbruck and Korea University College of Medicine. Together, these results define anatomically distinct evolutionary trajectories of GBM and underscore how spatial context shapes molecular diversity, clinical behavior, and imaging manifestations. This spatially integrated framework provides a foundation for precision oncology approaches that incorporate spatial evolutionary constraints into therapeutic stratification. Citation Format: You Jin Song, Yelyzaveta Miller-Michlits, Karl-Heinz Nenning, Christoph Bock, Ji Yoon Lee, Jiwon Kim, Jisoo Hong, Dayoung Lee, Namsung Moon, Harim Koo, Jason K. Sa, Adelheid Woehrer. Spatially resolved genomics reveals evolutionary modes and imaging correlates in glioblastoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 694.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-694
Primary Topic
Radiomics and Machine Learning in Medical Imaging
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 694: Spatially resolved genomics reveals evolutionary modes and imaging correlates in glioblastoma.

Adelheid Wöehrer, D. H. Lee, You Jin Song, Christoph Bock et al.
Cancer Research
Radiomics and Machine Learning in Medical Imaging
article

Abstract 694: Spatially resolved genomics reveals evolutionary modes and imaging correlates in glioblastoma.

Adelheid Wöehrer, D. H. Lee, You Jin Song, Christoph Bock, Yelyzaveta Miller-Michlits, Harim Koo, Karl‐Heinz Nenning, Jisoo Hong, Namsung Moon, Jason K. Sa, Jiwon Kim, Ji Yoon Lee
article en

Abstract

Abstract The spatial evolutionary dynamics of glioblastoma remain poorly understood. Here, we performed spatially resolved molecular profiling of 78 multi-regional tumor specimens from 24 GBM patients by integrating neuro-navigation-guided intraoperative sampling with deep whole-exome sequencing. This dataset represents one of the most spatially detailed genomic resources for GBM to date. By coupling spatial coordinates with genomic complexity, we delineated two distinct evolutionary trajectories: an “Expansive” model, in which three-dimensional growth and molecular diversification proceed in parallel, and a “Stochastic” model, where genomic diversification occurs independently of spatial expansion. These models were supported by phylogenetic reconstruction and radiogenomic analyses, revealing how spatial architecture constrains clonal dynamics. Quantitative integration of molecular and physical distances uncovered that tumors with greater spatially correlated genomic diversity exhibited worse clinical outcomes. Patients harboring “Stochastic” tumors demonstrated inferior survival probabilities compared to those with “Expansive” tumors, suggesting that spatially derived molecular metrics may serve as prognostic indicators of tumor aggressiveness. Furthermore, MRI-derived radiomic features, particularly texture-based metrics from T1-contrast enhanced images, mirrored underlying genomic complexity and aligned with evolutionary modes, establishing a link between intratumoral heterogeneity and noninvasive imaging phenotypes. While prior genomic studies have characterized GBM evolution at the molecular level, most lacked spatial resolution and failed to capture the three-dimensional architecture of tumor growth within the human brain. Our study overcomes this limitation through an international collaboration between the Medical University of Innsbruck and Korea University College of Medicine. Together, these results define anatomically distinct evolutionary trajectories of GBM and underscore how spatial context shapes molecular diversity, clinical behavior, and imaging manifestations. This spatially integrated framework provides a foundation for precision oncology approaches that incorporate spatial evolutionary constraints into therapeutic stratification. Citation Format: You Jin Song, Yelyzaveta Miller-Michlits, Karl-Heinz Nenning, Christoph Bock, Ji Yoon Lee, Jiwon Kim, Jisoo Hong, Dayoung Lee, Namsung Moon, Harim Koo, Jason K. Sa, Adelheid Woehrer. Spatially resolved genomics reveals evolutionary modes and imaging correlates in glioblastoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 694.

Cancer ResearchVol. 86(7_Supplement)
Ulsan College (KR), Nathan Kline Institute for Psychiatric Research (US), Austrian Academy of Sciences (AT), Innsbruck Medical University (AT), Universität Innsbruck (AT), Korea University (KR), University of Ulsan (KR)
Partnerships for the goals
Openalex Percentile: Top 4%
Radiomics and Machine Learning in Medical Imaging
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.