Abstract

ObjectivesReusing baseline volumes of interest (VOI) by applying non-rigid and to some extent (local) rigid image registration showed good test-retest variability similar to delineating VOI on both scans individually. The aim of the present study was to compare response assessments and classifications based on various types of image registration with those based on (semi)-automatic tumour delineation.MethodsBaseline (n = 13), early (n = 12) and late (n = 9) response (after one and three cycles of treatment, respectively) whole body [18F]fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography (PET/CT) scans were acquired in subjects with advanced gastrointestinal malignancies. Lesions were identified for early and late response scans. VOI were drawn independently on all scans using an adaptive 50% threshold method (A50). In addition, various types of (non-)rigid image registration were applied to PET and/or CT images, after which baseline VOI were projected onto response scans. Response was classified using PET Response Criteria in Solid Tumors for maximum standardized uptake value (SUVmax), average SUV (SUVmean), peak SUV (SUVpeak), metabolically active tumour volume (MATV), total lesion glycolysis (TLG) and the area under a cumulative SUV-volume histogram curve (AUC).ResultsNon-rigid PET-based registration and non-rigid CT-based registration followed by non-rigid PET-based registration (CTPET) did not show differences in response classifications compared to A50 for SUVmax and SUVpeak,, however, differences were observed for MATV, SUVmean, TLG and AUC. For the latter, these registrations demonstrated a poorer performance for small lung lesions (<2.8 ml), whereas A50 showed a poorer performance when another area with high uptake was close to the target lesion. All methods were affected by lesions with very heterogeneous tracer uptake.ConclusionsNon-rigid PET- and CTPET-based image registrations may be used to classify response based on SUVmax and SUVpeak. For other quantitative measures future studies should assess which method is valid for response evaluations by correlating with survival data.

Highlights

  • Positron emission tomography/computed tomography (PET/ CT) has been shown to be a valuable tool in oncology for monitoring response to treatment [1]

  • One practical issue with longitudinal positron emission tomography/computed tomography (PET/CT) studies is that patient positioning between consecutive scans may vary, thereby inhibiting the direct reuse of baseline Volumes of interest (VOI) for response scans

  • Dice similarity coefficients (DSC) values obtained from lung VOI were significantly higher for non-rigid image registration compared to rigid registration (p,0.04, figures 1C and 1D), except in early response assessments using local PET registration compared to non-rigid PET registration (p = 0.10)

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Summary

Introduction

Positron emission tomography/computed tomography (PET/ CT) has been shown to be a valuable tool in oncology for monitoring response to treatment [1]. A previous test-retest study showed that reusing baseline VOI by applying non-rigid and to lesser extent (local) rigid image registration has good repeatability, similar to delineating VOI on either scan separately [8]. In a test-retest setting, no changes in tumour shape, volume, tracer uptake and/or tracer uptake heterogeneity are expected, because these studies are acquired within a limited time frame and without administration of therapy. In a response monitoring setting, the interval between consecutive scans can be several weeks For this reason, difference in patient positioning between consecutive PET/CT scans may pose a challenge for image registration strategies in longitudinal PET/CT studies, and changes in tumour shape, volume, tracer uptake and tracer uptake heterogeneity, resulting from either treatment effects or progression of the disease [8,9]

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