Post-treatment FDG PET-CT in head and neck carcinoma: comparative analysis of 4 qualitative interpretative criteria in a large patient cohort.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 03 2020
Historique:
received: 04 09 2019
accepted: 12 02 2020
entrez: 7 3 2020
pubmed: 7 3 2020
medline: 24 11 2020
Statut: epublish

Résumé

There is no consensus regarding optimal interpretative criteria (IC) for Fluorine-18 fluorodeoxyglucose (FDG) Positron Emission Tomography - Computed Tomography (PET-CT) response assessment following (chemo)radiotherapy (CRT) for head and neck squamous cell carcinoma (HNSCC). The aim was to compare accuracy of IC (NI-RADS, Porceddu, Hopkins, Deauville) for predicting loco-regional control and progression free survival (PFS). All patients with histologically confirmed HNSCC treated at a specialist cancer centre with curative-intent non-surgical treatment who underwent baseline and response assessment FDG PET-CT between August 2008 and May 2017 were included. Metabolic response was assessed using 4 different IC harmonised into 4-point scales (complete response, indeterminate, partial response, progressive disease). IC performance metrics (sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), accuracy) were compared. Kaplan-Meier and Cox proportional hazards regression analyses were performed for survival analysis. 562 patients were included (397 oropharynx, 53 hypopharynx, 48 larynx, 64 other/unknown primary). 420 patients (75%) received CRT and 142 (25%) had radiotherapy alone. Median follow-up was 26 months (range 3-148). 156 patients (28%) progressed during follow-up. All IC were accurate for prediction of primary tumour (mean NPV 85.0% (84.6-85.3), PPV 85.0% (82.5-92.3), accuracy 84.9% (84.2-86.0)) and nodal outcome (mean NPV 85.6% (84.1-86.6), PPV 94.7% (93.8-95.1), accuracy 86.8% (85.6-88.0)). Number of indeterminate scores for NI-RADS, Porceddu, Deauville and Hopkins were 91, 25, 20, 13 and 55, 70, 18 and 3 for primary tumour and nodes respectively. PPV was significantly reduced for indeterminate uptake across all IC (mean PPV primary tumour 36%, nodes 48%). Survival analyses showed significant differences in PFS between response categories classified by each of the four IC (p <0.001). All four IC have similar diagnostic performance characteristics although Porceddu and Deauville scores offered the best trade off of minimising indeterminate outcomes whilst maintaining a high NPV.

Identifiants

pubmed: 32139722
doi: 10.1038/s41598-020-60739-3
pii: 10.1038/s41598-020-60739-3
pmc: PMC7058010
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4086

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Auteurs

Jim Zhong (J)

Department of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK. Jim.zhong@nhs.net.
Department of Nuclear Medicine, St James's Institute of Oncology, Leeds, UK. Jim.zhong@nhs.net.

Moses Sundersingh (M)

Department of Clinical Oncology, St James's Institute of Oncology, Leeds, UK.

Karen Dyker (K)

Department of Clinical Oncology, St James's Institute of Oncology, Leeds, UK.

Stuart Currie (S)

Department of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.

Sriram Vaidyanathan (S)

Department of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Department of Nuclear Medicine, St James's Institute of Oncology, Leeds, UK.

Robin Prestwich (R)

Department of Clinical Oncology, St James's Institute of Oncology, Leeds, UK.

Andrew Scarsbrook (A)

Department of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Department of Nuclear Medicine, St James's Institute of Oncology, Leeds, UK.
Leeds Institute of Medical Research at St James's, Faculty of Medicine & Health, University of Leeds, Leeds, UK.

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