Evidence map›Paper›PMID 35129651›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2022

The diagnostic accuracy and clinical impact of FDG-PET/CT follow-up for patients on adjuvant immunotherapy for high-risk malignant melanoma.

Jesper A S Andersen, Anders D Spatzek, Mie H Vilstrup, Peter Grupe, Søren Hess, Paw C Holdgaard, Lars Bastholt, Oke Gerke, Malene G Hildebrandt

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Article in European journal of nuclear medicine and molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Jesper A S AndersenDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Anders D SpatzekDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Mie H VilstrupDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Peter GrupeDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Søren HessDepartment of Radiology and Nuclear Medicine, Hospital South West Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark.
Paw C HoldgaardDepartment of Nuclear Medicine, University Hospital Lillebaelt, Vejle, Denmark.
Lars BastholtDepartment of Oncology, Odense University Hospital, Odense, Denmark.
Oke GerkeDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Malene G HildebrandtDepartment of Nuclear Medicine, Odense University Hospital, Odense, Denmark. Malene.Grubbe.Hildebrandt@rsyd.dk.
Odense University Hospital · DKUniversity of Southern Denmark · DKLillebaelt Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe benefit of FDG-PET/CT in follow-up of patients treated with adjuvant immunotherapy after resection of high-risk malignant melanoma (MM) is debated. This study evaluated the diagnostic accuracy and clinical impact of FDG-PET/CT for diagnosing MM recurrence during the first year after surgery.

methodsWe retrospectively included 124 patients with resected high-risk MM, who received adjuvant immunotherapy and follow-up FDG-PET/CT. Clinical information and AJCC-8 stage was obtained from patients' medical records. Recurrence was verified by biopsy/progression on a subsequent scan leading to change of treatment. Non-recurrence was assumed when no metastases were observed until the subsequent follow-up scan. Incidence of recurrence, sensitivity, specificity, positive and negative predictive values (PPV and NPV) were outcome measures.

resultsIncidence rate of MM recurrence was 0.27 [95% CI 0.17-0.37] per person-year during the first-year. Recurrence was detected in 13 patients (10%) at 3-month FDG-PET/CT, in 10 patients (8.1%) at 6 months, 1 patient (0.8%) at 9 months, 3 patients (2.4%) at 12 months. The overall sensitivity, specificity, PPV, and NPV were 97% [86-99], 82% [78-86], 39% [29-50], and 99% [98-99], respectively. The PPV trended towards higher values as disease stage increased. At the 3-month scan, the majority of actions derived from positive findings were surgery or earlier expedition of the subsequent follow-up scan.

conclusionThe high rate of recurrence in patients with high-risk MM treated with adjuvant immunotherapy emphasizes the need for follow-up. The potential harm by a moderately low specificity reflecting a high number of false-positive results must be weighed against the benefit of early detection of recurrence.

Indexed as

Fluorodeoxyglucose F18MelanomaCutaneous Malignant MelanomaFollow-Up StudiesHumansImmunotherapyNeoplasm Recurrence, LocalPositron Emission Tomography Computed TomographyRadiopharmaceuticalsRetrospective StudiesSensitivity and SpecificitySkin NeoplasmsFluorodeoxyglucose F18RadiopharmaceuticalsAdjuvant immunotherapyCohort studyFDG-PET/CTFollow-upMelanomaMonitoringRegister

Identifiers

PMID35129651
OpenAlexW4210834994

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Registered trials

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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.