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Updated: May 7, 2026

Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
Published on: July 31, 2017
Preoperative prediction of Ki-67 expression and risk stratification in gliomas using multiparametric MRI and
Xingrui Wang1, Hao Wu2, Yuanzheng Wang1
1Department of Radiology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Purpose:
To investigate the feasibility of multiparametric magnetic resonance imaging (MRI)-based characterization of intratumor heterogeneity (ITH) for noninvasive prediction of Ki-67 proliferation index (PI) and assessment of its prognostic significance in gliomas.
Materials And Methods:
This study included 205 patients with pathologically confirmed gliomas. Dynamic contrast-enhanced MRI and diffusion-weighted imaging were used to generate volume transfer constant (K trans ) and apparent diffusion coefficient (ADC) maps. A voxel-wise k -means clustering algorithm was applied to segment tumors into three biologically distinct intratumor habitats based on K trans and ADC values. Logistic regression and elastic net models were developed to predict Ki-67 PI. Model performance was validated through 10-fold cross-validation (CV) and two independent test cohorts, with diagnostic accuracy assessed by receiver operating characteristic curves and area under the curve (AUC). The prognostic value of habitat-derived biomarkers for progression-free survival (PFS) and overall survival (OS) was evaluated using Kaplan-Meier analysis and Cox proportional hazards models. A composite risk score was calculated for patient stratification.
Results:
Three spatial habitats were identified: H1 (hypo-vasopermeability, hypo-cellularity habitat), H2 (hypo-vasopermeability, hypercellularity habitat), and H3 (hyper-vasopermeability habitat). The elastic net model demonstrated high predictive accuracy for Ki-67 PI, with AUCs of 0.924, 0.875, 0.881, and 0.869 in the training, CV, and two test sets, respectively. Patients classified as high-risk by the risk score exhibited markedly shorter PFS (median 6.3 vs. 52.4 months) and OS (median 13.2 vs. 76.4 months) compared to low-risk patients. High-risk status was significantly associated with poorer prognosis [PFS: hazard ratio (HR) = 4.338, 95% confidence interval (CI): 2.596-7.249; OS: HR = 4.471, 95% CI: 2.572-7.772; both P < 0.001).
Conclusion:
Multiparametric MRI-based habitat imaging effectively enables preoperative noninvasive prediction of Ki-67 expression and risk stratification in gliomas, with potential to offer insights into tumor biological behavior and inform individualized treatment planning.
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