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Spatial mapping of tumor heterogeneity in whole-body PET–CT: a feasibility study

Tumor heterogeneity is recognized as a predictor of treatment response and patient outcome. Quantification of tumor heterogeneity across all scales may therefore provide critical insight that ultimately improves cancer management. An image registration-based framework for the study of tumor heteroge...

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Published in:Biomedical engineering online 2023-11, Vol.22 (1), p.1-110, Article 110
Main Authors: Jönsson, Hanna, Ahlström, Håkan, Kullberg, Joel
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description Tumor heterogeneity is recognized as a predictor of treatment response and patient outcome. Quantification of tumor heterogeneity across all scales may therefore provide critical insight that ultimately improves cancer management. An image registration-based framework for the study of tumor heterogeneity in whole-body images was evaluated on a dataset of 490 FDG-PET-CT images of lung cancer, lymphoma, and melanoma patients. Voxel-, lesion- and subject-level features were extracted from the subjects' segmented lesion masks and mapped to female and male template spaces for voxel-wise analysis. Resulting lesion feature maps of the three subsets of cancer patients were studied visually and quantitatively. Lesion volumes and lesion distances in subject spaces were compared with resulting properties in template space. The strength of the association between subject and template space for these properties was evaluated with Pearson's correlation coefficient. Spatial heterogeneity in terms of lesion frequency distribution in the body, metabolic activity, and lesion volume was seen between the three subsets of cancer patients. Lesion feature maps showed anatomical locations with low versus high mean feature value among lesions sampled in space and also highlighted sites with high variation between lesions in each cancer subset. Spatial properties of the lesion masks in subject space correlated strongly with the same properties measured in template space (lesion volume, R = 0.986, p < 0.001; total metabolic volume, R = 0.988, p < 0.001; maximum within-patient lesion distance, R = 0.997, p < 0.001). Lesion volume and total metabolic volume increased on average from subject to template space (lesion volume, 3.1 [+ or -] 52 ml; total metabolic volume, 53.9 [+ or -] 229 ml). Pair-wise lesion distance decreased on average by 0.1 [+ or -] 1.6 cm and maximum within-patient lesion distance increased on average by 0.5 [+ or -] 2.1 cm from subject to template space. Spatial tumor heterogeneity between subsets of interest in cancer cohorts can successfully be explored in whole-body PET-CT images within the proposed framework. Whole-body studies are, however, especially prone to suffer from regional variation in lesion frequency, and thus statistical power, due to the non-uniform distribution of lesions across a large field of view.
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Quantification of tumor heterogeneity across all scales may therefore provide critical insight that ultimately improves cancer management. An image registration-based framework for the study of tumor heterogeneity in whole-body images was evaluated on a dataset of 490 FDG-PET-CT images of lung cancer, lymphoma, and melanoma patients. Voxel-, lesion- and subject-level features were extracted from the subjects' segmented lesion masks and mapped to female and male template spaces for voxel-wise analysis. Resulting lesion feature maps of the three subsets of cancer patients were studied visually and quantitatively. Lesion volumes and lesion distances in subject spaces were compared with resulting properties in template space. The strength of the association between subject and template space for these properties was evaluated with Pearson's correlation coefficient. Spatial heterogeneity in terms of lesion frequency distribution in the body, metabolic activity, and lesion volume was seen between the three subsets of cancer patients. Lesion feature maps showed anatomical locations with low versus high mean feature value among lesions sampled in space and also highlighted sites with high variation between lesions in each cancer subset. Spatial properties of the lesion masks in subject space correlated strongly with the same properties measured in template space (lesion volume, R = 0.986, p &lt; 0.001; total metabolic volume, R = 0.988, p &lt; 0.001; maximum within-patient lesion distance, R = 0.997, p &lt; 0.001). Lesion volume and total metabolic volume increased on average from subject to template space (lesion volume, 3.1 [+ or -] 52 ml; total metabolic volume, 53.9 [+ or -] 229 ml). Pair-wise lesion distance decreased on average by 0.1 [+ or -] 1.6 cm and maximum within-patient lesion distance increased on average by 0.5 [+ or -] 2.1 cm from subject to template space. Spatial tumor heterogeneity between subsets of interest in cancer cohorts can successfully be explored in whole-body PET-CT images within the proposed framework. Whole-body studies are, however, especially prone to suffer from regional variation in lesion frequency, and thus statistical power, due to the non-uniform distribution of lesions across a large field of view.</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><doi>10.1186/s12938-023-01173-0</doi><oa>free_for_read</oa></addata></record>
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subjects Abdomen
Cancer
Care and treatment
Computed tomography
Correlation coefficient
Correlation coefficients
CT imaging
Diagnosis
Evaluation
Feasibility studies
Feature maps
Females
Frequency distribution
Frequency variation
Heterogeneity
Heterogeneous catalysis
Image registration
Lesions
Lung cancer
Lymphoma
Males
Mapping
Masks
Medical imaging
Medical imaging equipment
Medical research
Medicine, Experimental
Melanoma
Metabolism
Metastasis
Non-Hodgkin's lymphomas
Patients
PET imaging
Positron emission
Radiomics
Registration
Spatial heterogeneity
Standard deviation
Tomography
Tumor distribution
Tumor heterogeneity
Tumors
Voxel-wise analysis
Whole-body PET-CT
title Spatial mapping of tumor heterogeneity in whole-body PET–CT: a feasibility study
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