Evaluation of various apparent diffusion coefficient measurement techniques in pre-operative staging of early cervical carcinoma.


Journal

European journal of radiology
ISSN: 1872-7727
Titre abrégé: Eur J Radiol
Pays: Ireland
ID NLM: 8106411

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 08 02 2019
revised: 21 06 2019
accepted: 25 06 2019
entrez: 24 8 2019
pubmed: 24 8 2019
medline: 18 12 2019
Statut: ppublish

Résumé

DW-MRI parameters such as ADC hold the potential for more reliable staging of cervical cancer. We compared 2D region of interest (ROI) measurement techniques to 3D tumor analysis in the evaluation of ADC for cervical cancer. Secondly, we evaluated the utility of ADC for assessing parametrial and/or lymph node involvement. This prospective patient cohort registered cervical cancer patients who underwent pre-operative MRI with T1, T2W, and axial DWI. Retrospectively, two observers independently and blindly scored mean, minimum, and maximum ADC using three methods: a) 3D-Tumor analysis, b) single freehand ROI (2D-Slice), and c) single circular ROI (2D-Circle). Another observer scored parametrial and lymph node involvement on T1/T2W sequences. Parametrial and/or lymph node involvement were determined by surgical-pathologic results. The diagnostic performance of ADC for predicting the latter was evaluated by ROC curve, uni and multivariate analyses. Of 58 included patients, parametrial and/or lymph node involvement was found in 9 and 11 patients, respectively. Mean ADC (ADC Single ROI measurements are a reliable method for determining ADC

Identifiants

pubmed: 31439228
pii: S0720-048X(19)30225-6
doi: 10.1016/j.ejrad.2019.06.021
pii:
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101-106

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

J E Mongula (JE)

Maastricht University Medical Center, Department of Obstetrics and Gynecology, Postbus 5800, 6202 AZ, Maastricht, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: jordy.mongula@mumc.nl.

F Bakers (F)

Maastricht University Medical Center, Department of Radiology, Maastricht, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: fch.bakers@mumc.nl.

B F M Slangen (BFM)

Maastricht University Medical Center, Department of Obstetrics and Gynecology, Postbus 5800, 6202 AZ, Maastricht, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: brigitte.slangen@mumc.nl.

S M J van Kuijk (SMJ)

Maastricht University Medical Center, Department of Clinical Epidemiology and Medical Technology Assessment, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: sander.van.kuijk@mumc.nl.

R F P M Kruitwagen (RFPM)

Maastricht University Medical Center, Department of Obstetrics and Gynecology, Postbus 5800, 6202 AZ, Maastricht, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: r.kruitwagen@mumc.nl.

C Mihl (C)

Maastricht University Medical Center, Department of Radiology, Maastricht, the Netherlands; GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, the Netherlands. Electronic address: casper.mihl@mumc.nl.

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