Quantitative evaluation of the influence of multiple MRI sequences and of pathological tissues on the registration of longitudinal data acquired during brain tumor treatment.

MRI brain convolutional neural network deep learning image registration tumor

Journal

Frontiers in neuroimaging
ISSN: 2813-1193
Titre abrégé: Front Neuroimaging
Pays: Switzerland
ID NLM: 9918402387106676

Informations de publication

Date de publication:
2022
Historique:
received: 24 06 2022
accepted: 15 08 2022
medline: 9 8 2023
pubmed: 9 8 2023
entrez: 9 8 2023
Statut: epublish

Résumé

Registration methods facilitate the comparison of multiparametric magnetic resonance images acquired at different stages of brain tumor treatments. Image-based registration solutions are influenced by the sequences chosen to compute the distance measure, and the lack of image correspondences due to the resection cavities and pathological tissues. Nonetheless, an evaluation of the impact of these input parameters on the registration of longitudinal data is still missing. This work evaluates the influence of multiple sequences, namely T1-weighted (T1), T2-weighted (T2), contrast enhanced T1-weighted (T1-CE), and T2 Fluid Attenuated Inversion Recovery (FLAIR), and the exclusion of the pathological tissues on the non-rigid registration of pre- and post-operative images. We here investigate two types of registration methods, an iterative approach and a convolutional neural network solution based on a 3D U-Net. We employ two test sets to compute the mean target registration error (mTRE) based on corresponding landmarks. In the first set, markers are positioned exclusively in the surroundings of the pathology. The methods employing T1-CE achieves the lowest mTREs, with a improvement up to 0.8 mm for the iterative solution. The results are higher than the baseline when using the FLAIR sequence. When excluding the pathology, lower mTREs are observable for most of the methods. In the second test set, corresponding landmarks are located in the entire brain volumes. Both solutions employing T1-CE obtain the lowest mTREs, with a decrease up to 1.16 mm for the iterative method, whereas the results worsen using the FLAIR. When excluding the pathology, an improvement is observable for the CNN method using T1-CE. Both approaches utilizing the T1-CE sequence obtain the best mTREs, whereas the FLAIR is the least informative to guide the registration process. Besides, the exclusion of pathology from the distance measure computation improves the registration of the brain tissues surrounding the tumor. Thus, this work provides the first numerical evaluation of the influence of these parameters on the registration of longitudinal magnetic resonance images, and it can be helpful for developing future algorithms.

Identifiants

pubmed: 37555157
doi: 10.3389/fnimg.2022.977491
pmc: PMC10406206
doi:

Types de publication

Journal Article

Langues

eng

Pagination

977491

Informations de copyright

Copyright © 2022 Canalini, Klein, Waldmannstetter, Kofler, Cerri, Hering, Heldmann, Schlaeger, Menze, Wiestler, Kirschke and Hahn.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Luca Canalini (L)

Fraunhofer Institute for Digital Medicine MEVIS, Bremen, Germany.

Jan Klein (J)

Fraunhofer Institute for Digital Medicine MEVIS, Bremen, Germany.

Diana Waldmannstetter (D)

Image-Based Biomedical Modeling, Department of Informatics, Technical University of Munich, Munich, Germany.
Department of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.

Florian Kofler (F)

Image-Based Biomedical Modeling, Department of Informatics, Technical University of Munich, Munich, Germany.
Department of Neuroradiology, Technical University of Munich (TUM) School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
TranslaTUM - Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.
Helmholtz AI, Helmholtz Zentrum Munich, Munich, Germany.

Stefano Cerri (S)

Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

Alessa Hering (A)

Fraunhofer Institute for Digital Medicine MEVIS, Lübeck, Germany.
Diagnostic Image Analysis Group, Radboud University Medical Center, Nijmegen, Netherlands.

Stefan Heldmann (S)

Fraunhofer Institute for Digital Medicine MEVIS, Lübeck, Germany.

Sarah Schlaeger (S)

Department of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.
TranslaTUM - Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.

Bjoern H Menze (BH)

Image-Based Biomedical Modeling, Department of Informatics, Technical University of Munich, Munich, Germany.
Department of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.

Benedikt Wiestler (B)

Department of Neuroradiology, Technical University of Munich (TUM) School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
TranslaTUM - Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.

Jan Kirschke (J)

Department of Neuroradiology, Technical University of Munich (TUM) School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
TranslaTUM - Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.

Horst K Hahn (HK)

Fraunhofer Institute for Digital Medicine MEVIS, Bremen, Germany.

Classifications MeSH