Abstract

The aim of the current study was to investigate the diagnostic performance of FDG PET/MR compared to PET/CT in a patient cohort including Hodgkins lymphoma, diffuse large B-cell lymphoma, and high-grade B-cell lymphoma at baseline and response assessment. Sixty-one patients were examined with FDG PET/CT directly followed by PET/MR. Images were read by two pairs of nuclear medicine physicians and radiologists. Concordance for lymphoma involvement between PET/MR and the reference standard PET/CT was assessed at baseline and response assessment. Correlation of prognostic biomarkers Deauville score, criteria of response, SUVmax, SUVpeak, and MTV was performed between PET/MR and PET/CT. Baseline FDG PET/MR showed a sensitivity of 92.5% and a specificity 97.9% compared to the reference standard PET/CT (κ 0.91) for nodal sites. For extranodal sites, a sensitivity of 80.4% and a specificity of 99.5% were found (κ 0.84). Concordance in Ann Arbor was found in 57 of 61 patients (κ 0.92). Discrepancies were due to misclassification of region and not lesion detection. In response assessment, a sensitivity of 100% and a specificity 99.9% for all sites combined were found (κ 0.92). There was a perfect agreement on Deauville scores 4 and 5 and criteria of response between the two modalities. Intraclass correlation coefficient (ICC) for SUVmax, SUVpeak, and MTV values showed excellent reliability (ICC > 0.9). FDG PET/MR is a reliable alternative to PET/CT in this patient population, both in terms of lesion detection at baseline staging and response assessment, and for quantitative prognostic imaging biomarkers.

Highlights

  • The goal of treatment for Hodgkins lymphoma (HL), diffuse large B-cell lymphoma (DLBCL), and high-grade B-cell lymphoma is most often cure

  • Kappa agreement of extranodal sites combined was κ 0.91 for positron emission tomography (PET)/computed tomography (CT) and κ 0.96 for PET/MR

  • Inter-observer agreement on disease stage in terms of Ann Arbor I–II versus III–IV was on PET/CT κ 0.89 and κ 0.93 on PET/MR

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Summary

Introduction

The goal of treatment for Hodgkins lymphoma (HL), diffuse large B-cell lymphoma (DLBCL), and high-grade B-cell lymphoma is most often cure. Accurate staging at baseline and response assessment is essential for optimal treatment strategies. Risk stratification and treatment decisions require reliable prognostic imaging biomarkers in addition to pretreatment clinical risk assessment scores. Response adaptive FDG PET/CT guided treatment approach to evaluate chemosensitivity and to guide decision of radiotherapy allows for individual treatment strategies in HL [1, 2]. End of treatment response FDG PET/CT for detecting residual disease in DLBCL is an important prognostic factor and guides indication for consolidation radiotherapy [3]

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