Correlation between rCBV Delineation Similarity and Overall Survival in a Prospective Cohort of High-Grade Gliomas Patients: The Hidden Value of Multimodal MRI?

MRI PET-FET [18F]-FET PET/CT delineation glioblastoma high-grade gliomas magnetic resonance imaging rCBV radiotherapy

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
03 Apr 2024
Historique:
received: 08 03 2024
revised: 18 03 2024
accepted: 26 03 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

The accuracy of target delineation in radiation treatment planning of high-grade gliomas (HGGs) is crucial to achieve high tumor control, while minimizing treatment-related toxicity. Magnetic resonance imaging (MRI) represents the standard imaging modality for delineation of gliomas with inherent limitations in accurately determining the microscopic extent of tumors. The purpose of this study was to assess the survival impact of multi-observer delineation variability of multiparametric MRI (mpMRI) and [ Thirty prospectively included patients with histologically confirmed HGGs underwent a PET/CT and mpMRI including diffusion-weighted imaging (DWI: b0, b1000, ADC), contrast-enhanced T1-weighted imaging (T1-Gado), T2-weighted fluid-attenuated inversion recovery (T2Flair), and perfusion-weighted imaging with computation of relative cerebral blood volume (rCBV) and K2 maps. Nine radiation oncologists delineated the PET/CT and MRI sequences. Spatial similarity (Dice similarity coefficient: DSC) was calculated between the readers for each sequence. Impact of the DSC on progression-free survival (PFS) and overall survival (OS) was assessed using Kaplan-Meier curves and the log-rank test. The highest DSC mean values were reached for morphological sequences, ranging from 0.71 +/- 0.18 to 0.84 +/- 0.09 for T2Flair and T1Gado, respectively, while metabolic volumes defined by PET/CT achieved a mean DSC of 0.75 +/- 0.11. rCBV variability (mean DSC0.32 +/- 0.20) significantly impacted PFS ( Our data suggest that the T1-Gado and T2Flair sequences were the most reproducible sequences, followed by PET/CT. Reproducibility for functional sequences was low, but rCBV inter-reader similarity significantly impacted PFS and OS.

Identifiants

pubmed: 38672146
pii: biomedicines12040789
doi: 10.3390/biomedicines12040789
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Amina Latreche (A)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Gurvan Dissaux (G)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Solène Querellou (S)

Nuclear Medicine Department, University Hospital, 29200 Brest, France.
Groupe d'Etude de la Thrombose Occidentale GETBO (INSERM UMR 1304), Université de Bretagne Occidentale, 29200 Brest, France.

Doria Mazouz Fatmi (D)

Radiology Department, University Hospital, 29200 Brest, France.

François Lucia (F)

Radiation Oncology Department, University Hospital, 29200 Brest, France.
LaTIM UMR 1101, INSERM, Université de Bretagne Occidentale, 29200 Brest, France.

Anais Bordron (A)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Alicia Vu (A)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Ruben Touati (R)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Victor Nguyen (V)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Mohamed Hamya (M)

Radiation Oncology Department, University Hospital, 29200 Brest, France.

Brieg Dissaux (B)

Groupe d'Etude de la Thrombose Occidentale GETBO (INSERM UMR 1304), Université de Bretagne Occidentale, 29200 Brest, France.
Radiology Department, University Hospital, 29200 Brest, France.

Vincent Bourbonne (V)

Radiation Oncology Department, University Hospital, 29200 Brest, France.
LaTIM UMR 1101, INSERM, Université de Bretagne Occidentale, 29200 Brest, France.

Classifications MeSH