Evidence map›Paper›PMID 38062278›Full record

ArticleEJNMMI physics2023

Clinical application of a population-based input function (PBIF) for a shortened dynamic whole-body FDG-PET/CT protocol in patients with metastatic melanoma treated by immunotherapy.

Mathieu Pavoine, Philippe Thuillier, Nicolas Karakatsanis, Delphine Legoupil, Karim Amrane, Romain Floch, Romain Le Pennec, Pierre-Yves Salaün, Ronan Abgral, David Bourhis

Abstract read
In one paragraph

Article in EJNMMI physics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

10 authors.

Mathieu PavoineDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France.ORCID http://orcid.org/0009-0006-9972-3912
Philippe ThuillierUMR INSERM 1304 GETBO, Brest, France.
Nicolas KarakatsanisDepartment of Radiology, Weil Cornell Medical College of Cornell University, New York, NY, USA.
Delphine LegoupilDepartment of Dermatology, University Hospital, Brest, France.
Karim AmraneDepartment of Oncology, Regional Hospital, Morlaix, France.
Romain FlochDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France.
Romain Le PennecDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France.
Pierre-Yves SalaünDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France.
Ronan AbgralDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France.
David BourhisDepartment of Nuclear Medicine, University Hospital, 2 Avenue Foch, 29200, Brest, France. david.bourhis@chu-brest.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim was to investigate the feasibility of a shortened dynamic whole-body (dWB) FDG-PET/CT protocol and Patlak imaging using a population-based input function (PBIF), instead of an image-derived input function (IDIF) across the 60-min post-injection period, and study its effect on the FDG influx rate (Ki) quantification in patients with metastatic melanoma (MM) undergoing immunotherapy.

methodsThirty-seven patients were enrolled, including a PBIF modeling group (n = 17) and an independent validation cohort (n = 20) of MM from the ongoing prospective IMMUNOPET2 trial. All dWB-PET data were acquired on Vision 600 PET/CT systems. The PBIF was fitted using a Feng's 4-compartments model and scaled to the individual IDIF tail's section within the shortened acquisition time. The area under the curve (AUC) of PBIFs was compared to respective IDIFs AUC within 9 shortened time windows (TW) in terms of linear correlation (R

resultsThe mean ± SD relative AUC bias was calculated at 0.5 ± 3.8% (R

conclusionOur study showed the feasibility of a shortened dWB-PET imaging protocol with a PBIF approach, allowing to reduce acquisition duration from 70 to 20 min with reasonable bias. These findings open perspectives for its clinical use in routine practice such as treatment response assessment in oncology.

Indexed as

18F-FDGDynamic whole-body PETParametric imagingPBIF

Identifiers

PMID38062278
PMCPMC10703763

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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.