Added prognostic value of histogram features from preoperative multi-modal diffusion MRI in predicting Ki-67 proliferation for adult-type diffuse gliomas.

BACKGROUND

Ki-67 labelling index (LI), a critical marker of tumor proliferation, is vital for grading adult-type diffuse gliomas and predicting patient survival. However, its accurate assessment currently relies on invasive biopsy or surgical resection. This makes it challenging to non-invasively predict Ki-67 LI and subsequent prognosis. Therefore, this study aimed to investigate whether histogram analysis of multi-parametric diffusion model metrics-specifically diffusion tensor imaging (DTI), diffusion kurtosis imaging (DKI), and neurite orientation dispersion and density imaging (NODDI)-could help predict Ki-67 LI in adult-type diffuse gliomas and further predict patient survival.

METHODS

A total of 123 patients with diffuse gliomas who underwent preoperative bipolar spin-echo diffusion magnetic resonance imaging (MRI) were included. Diffusion metrics (DTI, DKI and NODDI) and their histogram features were extracted and used to develop a nomogram model in the training set (n=86), and the performance was verified in the test set (n=37). Area under the receiver operating characteristics curve of the nomogram model was calculated. The outcome cohort, including 123 patients, was used to evaluate the predictive value of the diffusion nomogram model for overall survival (OS). Cox proportion regression was performed to predict OS.

RESULTS

Among 123 patients, 87 exhibited high Ki-67 LI (Ki-67 LI >5%). The patients had a mean age of 46.08±13.24 years, with 39 being female. Tumor grading showed 46 cases of grade 2, 21 cases of grade 3, and 56 cases of grade 4. The nomogram model included eight histogram features from diffusion MRI and showed good performance for prediction Ki-67 LI, with area under the receiver operating characteristic curves (AUCs) of 0.92 [95% confidence interval (CI): 0.85-0.98, sensitivity =0.85, specificity =0.84] and 0.84 (95% CI: 0.64-0.98, sensitivity =0.77, specificity =0.73) in the training set and test set, respectively. Further nomogram incorporating these variables showed good discrimination in Ki-67 LI predicting and glioma grading. A low nomogram model score relative to the median value in the outcomes cohort was independently associated with OS (P<0.01).

CONCLUSIONS

Accurate prediction of the Ki-67 LI in adult-type diffuse glioma patients was achieved by using multi-modal diffusion MRI histogram radiomics model, which also reliably and accurately determined survival.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT06572592.