Interrater Agreement and Reliability of PERCIST and Visual Assessment When Using 18F-FDG-PET/CT for Response Monitoring of Metastatic Breast Cancer.

PERCIST PET/CT SULpeak agreement breast neoplasm inter-observer intra-observer

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
24 Nov 2020
Historique:
received: 07 10 2020
revised: 15 11 2020
accepted: 21 11 2020
entrez: 1 12 2020
pubmed: 2 12 2020
medline: 2 12 2020
Statut: epublish

Résumé

Response evaluation at regular intervals is indicated for treatment of metastatic breast cancer (MBC). FDG-PET/CT has the potential to monitor treatment response accurately. Our purpose was to: (a) compare the interrater agreement and reliability of the semi-quantitative PERCIST criteria to qualitative visual assessment in response evaluation of MBC and (b) investigate the intrarater agreement when comparing visual assessment of each rater to their respective PERCIST assessment. We performed a retrospective study on FDG-PET/CT in women who received treatment for MBC. Three specialists in nuclear medicine categorized response evaluation by qualitative assessment and standardized one-lesion PERCIST assessment. The scans were categorized into complete metabolic response, partial metabolic response, stable metabolic disease, and progressive metabolic disease. 37 patients with 179 scans were included. Visual assessment categorization yielded moderate agreement with an overall proportion of agreement (PoA) between raters of 0.52 (95% CI 0.44-0.66) and a Fleiss kappa estimate of 0.54 (95% CI 0.46-0.62). PERCIST response categorization yielded substantial agreement with an overall PoA of 0.65 (95% CI 0.57-0.73) and a Fleiss kappa estimate of 0.68 (95% CI 0.60-0.75). The difference in PoA between overall estimates for PERCIST and visual assessment was 0.13 (95% CI 0.06-0.21;

Identifiants

pubmed: 33255442
pii: diagnostics10121001
doi: 10.3390/diagnostics10121001
pmc: PMC7759893
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jonas S Sørensen (JS)

Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Mie H Vilstrup (MH)

Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Jorun Holm (J)

Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Marianne Vogsen (M)

Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.
Department of Oncology, Odense University Hospital, 5000 Odense, Denmark.
Odense Patient Data Explorative Network (OPEN), Odense University Hospital, 5000 Odense, Denmark.

Jakob L Bülow (JL)

Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Lasse Ljungstrøm (L)

Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Poul-Erik Braad (PE)

Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Oke Gerke (O)

Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.

Malene G Hildebrandt (MG)

Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, 5000 Odense, Denmark.
Odense Patient Data Explorative Network (OPEN), Odense University Hospital, 5000 Odense, Denmark.
Centre for Personalized Response Monitoring in Oncology (PREMIO), Odense University Hospital, 5000 Odense, Denmark.
Centre for Innovative Medical Technology (CIMT), Odense University Hospital, 5000 Odense, Denmark.

Classifications MeSH