MR Intensity Normalization Methods Impact Sequence Specific Radiomics Prognostic Model Performance in Primary and Recurrent High-Grade Glioma

Author:

Salome Patrick1234ORCID,Sforazzini Francesco123,Brugnara Gianluca5,Kudak Andreas467ORCID,Dostal Matthias467ORCID,Herold-Mende Christel89ORCID,Heiland Sabine5,Debus Jürgen346,Abdollahi Amir1346ORCID,Knoll Maximilian1346ORCID

Affiliation:

1. Clinical Cooperation Unit (CCU) Radiation Oncology, German Cancer Research Centre, INF 280, 69120 Heidelberg, Germany

2. Heidelberg Medical Faculty, Heidelberg University, 69120 Heidelberg, Germany

3. German Cancer Consortium (DKTK) Core Centre Heidelberg, 69120 Heidelberg, Germany

4. Heidelberg Ion-Beam Therapy Centre (HIT), INF 450, 69120 Heidelberg, Germany

5. Department of Neuroradiology, Heidelberg University Hospital, 69120 Heidelberg, Germany

6. Department of Radiation Oncology, Heidelberg University Hospital, INF 400, 69120 Heidelberg, Germany

7. CCU Radiation Therapy, German Cancer Research Centre, INF 280, 69120 Heidelberg, Germany

8. Brain Tumour Group, European Organization for Research and Treatment of Cancer, 1200 Brussels, Belgium

9. Division of Neurosurgical Research, Department of Neurosurgery, Heidelberg University Hospital, 69120 Heidelberg, Germany

Abstract

Purpose: This study investigates the impact of different intensity normalization (IN) methods on the overall survival (OS) radiomics models’ performance of MR sequences in primary (pHGG) and recurrent high-grade glioma (rHGG). Methods: MR scans acquired before radiotherapy were retrieved from two independent cohorts (rHGG C1: 197, pHGG C2: 141) from multiple scanners (15, 14). The sequences are T1 weighted (w), contrast-enhanced T1w (T1wce), T2w, and T2w-FLAIR. Sequence-specific significant features (SF) associated with OS, extracted from the tumour volume, were derived after applying 15 different IN methods. Survival analyses were conducted using Cox proportional hazard (CPH) and Poisson regression (POI) models. A ranking score was assigned based on the 10-fold cross-validated (CV) concordance index (C-I), mean square error (MSE), and the Akaike information criterion (AICs), to evaluate the methods’ performance. Results: Scatter plots of the 10-CV C-I and MSE against the AIC showed an impact on the survival predictions between the IN methods and MR sequences (C1/C2 C-I range: 0.62–0.71/0.61–0.72, MSE range: 0.20–0.42/0.13–0.22). White stripe showed stable results for T1wce (C1/C2 C-I: 0.71/0.65, MSE: 0.21/0.14). Combat (0.68/0.62, 0.22/0.15) and histogram matching (HM, 0.67/0.64, 0.22/0.15) showed consistent prediction results for T2w models. They were also the top-performing methods for T1w in C2 (Combat: 0.67, 0.13; HM: 0.67, 0.13); however, only HM achieved high predictions in C1 (0.66, 0.22). After eliminating IN impacted SF using Spearman’s rank-order correlation coefficient, a mean decrease in the C-I and MSE of 0.05 and 0.03 was observed in all four sequences. Conclusion: The IN method impacted the predictive power of survival models; thus, performance is sequence-dependent.

Funder

European Union’s Horizon 2020 research and innovation programme

collaborative research center of the German Research Foundation

Zentrum für Personalisierte Medizin

National Center for Tumor Diseases

German Cancer Consortium (DKTK) Radiation Oncology programs

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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