Evidence map›Paper›PMID 36694244›Full record

ArticleCancer imaging : the official publication of the International Cancer Imaging Society2023

Diagnostic performance of prospective same-day 18F-FDG PET/MRI and 18F-FDG PET/CT in the staging and response assessment of lymphoma.

Vijay Mistry, Justin R Scott, Tzu-Yang Wang, Peter Mollee, Kenneth A Miles, W Phillip Law, Greg Hapgood

Open access · goldAbstract read
In one paragraph

Article in Cancer imaging : the official publication of the International Cancer Imaging Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Vijay Mistry *Department of Medical Imaging, Princess Alexandra Hospital, Brisbane, Australia. vjmis3@gmail.com.ORCID http://orcid.org/0000-0002-3761-4714
Justin R ScottQCIF Bioinformatics, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia.
Tzu-Yang WangDepartment of Haematology, Princess Alexandra Hospital, Brisbane, Australia.
Peter MolleeDepartment of Haematology, Princess Alexandra Hospital, Brisbane, Australia.
Kenneth A MilesDepartment of Medical Imaging, Princess Alexandra Hospital, Brisbane, Australia.
W Phillip Law *Department of Medical Imaging, Princess Alexandra Hospital, Brisbane, Australia.
Greg Hapgood *Department of Haematology, Princess Alexandra Hospital, Brisbane, Australia.
Translational Research Institute · AUPrincess Alexandra Hospital · AUThe University of Queensland · AUUniversity of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate staging and response assessment are essential for prognosis and to guide treatment in patients with lymphoma. The aim of this study was to compare the diagnostic performance of FDG PET/MRI versus FDG PET/CT in adult patients with newly diagnosed Hodgkin and Non- Hodgkin lymphoma.

methodsIn this single centre study, 50 patients were prospectively recruited. FDG PET/MRI was performed after staging FDG PET/CT using a single injection of 18F-FDG. Patients were invited to complete same-day FDG PET/MRI with FDG PET/CT at interim and end of treatment response assessments. Performance was assessed using PET/CT as the reference standard for disease site identification, staging, response assessment with Deauville score and concordance in metabolic activity.

resultsStaging assessment showed perfect agreement (κ = 1.0, P = 0) between PET/MRI and PET/CT using Ann Arbor staging. There was excellent intermodality correlation with disease site identification at staging (κ = 0.976, P < 0.001) with FDG PET/MRI sensitivity of 96% (95% CI, 94-98%) and specificity of 100% (95% CI, 99-100%). There was good correlation of disease site identification at interim assessment (κ = 0.819, P < 0.001) and excellent correlation at end-of-treatment assessment (κ = 1.0, P < 0.001). Intermodality agreement for Deauville scores was good at interim assessment (κ = 0.808, P < 0.001) and excellent at end-of-treatment assessment (κ = 1.0, P = 0). There was good-excellent concordance in SUV max and mean between modalities across timepoints. Minimum calculated radiation patient effective dose saving was 54% between the two modalities per scan.

conclusionWith high concordance in disease site identification, staging and response assessment, PET/MR is a potentially viable alternative to PET/CT in lymphoma that minimises radiation exposure.

Indexed as

Fluorodeoxyglucose F18LymphomaAdultDiffusion Magnetic Resonance ImagingHumansMagnetic Resonance ImagingNeoplasm StagingPositron-Emission TomographyPositron Emission Tomography Computed TomographyProspective StudiesRadiopharmaceuticalsFluorodeoxyglucose F18Radiopharmaceuticals18F-FDGHodgkin lymphomaLymphomaNon-Hodgkin lymphomaPET/CTPET/MRI

Identifiers

PMID36694244
PMCPMC9872391
OpenAlexW4317908165

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.