Whole-body MRI in oncology: can a single anatomic T2 Dixon sequence replace the combination of T1 and STIR sequences to detect skeletal metastasis and myeloma?


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 09 02 2022
accepted: 30 06 2022
revised: 21 06 2022
pubmed: 5 8 2022
medline: 20 12 2022
entrez: 4 8 2022
Statut: ppublish

Résumé

To compare the diagnostic accuracy of a single T2 Dixon sequence to the combination T1+STIR as anatomical sequences used for detecting tumoral bone marrow lesions in whole-body MRI (WB-MRI) examinations. Between January 2019 and January 2020, seventy-two consecutive patients (55 men, 17 women, median age = 66 years) with solid (prostate, breast, neuroendocrine) cancers at high risk of metastasis or proven multiple myeloma (MM) prospectively underwent a WB-MRI examination including coronal T1, STIR, T2 Dixon and axial diffusion-weighted imaging sequences. Two radiologists independently assessed the combination of T1+STIR sequences and the fat+water reconstructions from the T2 Dixon sequence. The reference standard was established by consensus reading of WB-MRI and concurrent imaging available at baseline and at 6 months. Repeatability and reproducibility of MRI scores (presence and semi-quantitative count of lesions), image quality (SNR: signal-to-noise, CNR: contrast-to-noise, CRR: contrast-to-reference ratios), and diagnostic characteristics (Se: sensitivity, Sp: specificity, Acc: accuracy) were assessed per-skeletal region and per-patient. Repeatability and reproducibility were at least good regardless of the score, region, and protocol (0.67 ≤ AC1 ≤ 0.98). CRR was higher on T2 Dixon fat compared to T1 (p < 0.0001) and on T2 Dixon water compared to STIR (p = 0.0128). In the per-patient analysis, Acc of the T2 Dixon fat+water was higher than that of T1+STIR for the senior reader (Acc = +0.027 [+0.025; +0.029], p < 0.0001) and lower for the junior reader (Acc = -0.029 [-0.031; -0.027], p < 0.0001). A single T2 Dixon sequence with fat+water reconstructions offers similar reproducibility and diagnostic accuracy as the recommended combination of T1+STIR sequences and can be used for skeletal screening in oncology, allowing significant time-saving. • Replacement of the standard anatomic T1 + STIR WB-MRI protocol by a single T2 Dixon sequence drastically shortens the examination time without loss of diagnostic accuracy. • A protocol based on fat + water reconstructions from a single T2 Dixon sequence offers similar inter-reader agreement and a higher contrast-to-reference ratio for detecting lesions compared to the standard T1 + STIR protocol. • Differences in the accuracy between the two protocols are marginal (+ 3% in favor of the T2 Dixon with the senior reader; -3% against the T2 Dixon with the junior reader).

Identifiants

pubmed: 35925384
doi: 10.1007/s00330-022-09007-8
pii: 10.1007/s00330-022-09007-8
pmc: PMC9755082
doi:

Substances chimiques

Water 059QF0KO0R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

244-257

Informations de copyright

© 2022. The Author(s).

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Auteurs

Ophelye Chiabai (O)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Sandy Van Nieuwenhove (S)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Marie-Christiane Vekemans (MC)

Department of Internal Medicine, Hematology Unit, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Brussels, Belgium.

Bertrand Tombal (B)

Department of Surgery, Urology Unit, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Brussels, Belgium.

Frank Peeters (F)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Joris Wuts (J)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.
Department of Electronics and Informatics (ETRO), Vrije Universiteit Brussel, Brussels, Belgium.

Perrine Triqueneaux (P)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Patrick Omoumi (P)

Department of Radiology, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.

Thomas Kirchgesner (T)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Nicolas Michoux (N)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium.

Frédéric E Lecouvet (FE)

Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Institut de Recherche Expérimentale & Clinique (IREC), Université Catholique de Louvain (UCLouvain), Hippocrate Avenue, 10, B-1200, Brussels, Belgium. frederic.lecouvet@uclouvain.be.

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