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Esther G. C. Troost

Publications and source records attributed to Esther G. C. Troost.

2 recordsLinked to original sources

Combined photon-proton modeling of radiation-induced brain imaging changes supports variability in proton relative biological effectiveness and increased periventricular radiosensitivity

Purpose: Recent proton-only investigations of radiation-induced contrast enhancements (RICE) in brain tumor patients indicated variability in proton relative biological effectiveness (RBE) and increased radiosensitivity of the periventricular region (PVR). Because RBE is defined relative to a reference radiation, these studies required assumptions on the photon dose-response relationship. This study aimed to validate proton RBE variability and PVR radiosensitivity using predictive modeling of RICE in a combined photon-proton cohort. Methods and Materials: Predictive models for RICE detected on follow-up magnetic resonance imaging were developed in 152 intracranial tumor patients treated with photons or protons. Logistic regression was applied at the voxel level to model spatial occurrence and at the patient level to model incidence. A clinical RBE model was derived from voxel-wise comparisons of estimated risk between photon and proton irradiation. Results: In total, 128 RICE of various grades occurred in 64 patients. Voxel-level modeling validated absorbed dose (D), D multiplied by dose-averaged linear energy transfer (LETd) for proton therapy, and PVR as independent predictors of RICE. The model implied a variable proton RBE described by RBE=1+m$\cdot$LETd, with m=0.10 $μ$m/keV. At the patient level, the PVR D2ml based on this RBE achieved the highest predictive performance. Conclusions: RICE was spatially associated with dose and PVR proximity across photon and proton therapy, with an additional LET-dependent component after proton therapy. The cross-modality framework validates proton RBE variability against an observed photon reference rather than predefined reference assumptions, and supports PVR radiosensitivity as modality-independent. Accounting for variable proton RBE and the PVR as an organ at risk may improve risk assessment and mitigation of radiation-induced side effects.

physics.med-ph↗

Assessing robustness of radiomic features by image perturbation

Image features need to be robust against differences in positioning, acquisition and segmentation to ensure reproducibility. Radiomic models that only include robust features can be used to analyse new images, whereas models with non-robust features may fail to predict the outcome of interest accurately. Test-retest imaging is recommended to assess robustness, but may not be available for the phenotype of interest. We therefore investigated 18 methods to determine feature robustness based on image perturbations. Test-retest and perturbation robustness were compared for 4032 features that were computed from the gross tumour volume in two cohorts with computed tomography imaging: I) 31 non-small-cell lung cancer (NSCLC) patients; II): 19 head-and-neck squamous cell carcinoma (HNSCC) patients. Robustness was measured using the intraclass correlation coefficient (1,1) (ICC). Features with ICC$\geq0.90$ were considered robust. The NSCLC cohort contained more robust features for test-retest imaging than the HNSCC cohort ($73.5\%$ vs. $34.0\%$). A perturbation chain consisting of noise addition, affine translation, volume growth/shrinkage and supervoxel-based contour randomisation identified the fewest false positive robust features (NSCLC: $3.3\%$; HNSCC: $10.0\%$). Thus, this perturbation chain may be used to assess feature robustness.

cs.CV↗