Primary central nervous system lymphoma: advances in MRI and PET imaging.
Primary central nervous system lymphoma (PCNSL)
diffusion-weighted imaging (DWI)
magnetic resonance imaging (MRI)
positron emission tomography (PET)
Journal
Annals of lymphoma
Titre abrégé: Ann Lymphoma
Pays: China
ID NLM: 101718324
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
entrez:
22
8
2022
pubmed:
23
8
2022
medline:
23
8
2022
Statut:
ppublish
Résumé
Contrast enhanced magnetic resonance imaging (CE-MRI) remains the imaging modality of choice for initial workup, staging, and response assessment after therapy in patients with primary central nervous system lymphoma (PCNSL). While CE-MRI is a sensitive test to detect blood brain barrier (BBB) dysfunction, it does not biologically represent the true tumor burden. Current response assessment criteria relies heavily on two dimensional anatomical measurements on post contrast T1-weighted (T1W) images, as well as pre-contrast T2-weighted (T2W) imaging. Additional MRI features, such as diffusion-weighted imaging (DWI) and perfusion weighted imaging, can be routinely obtained at most centers with MRI capabilities. Emerging evidence supports the incorporation of these data to better define tumor physiology and provide additional valuable clinical tools capable of identifying high risk subgroups as well as early predictors of response to therapies. Further, novel advanced molecular and pathophysiologic characterization of PCNSL provides insights into promising targeted therapeutic approaches. However, significant institutional imaging variation and inconsistent clinical trial reporting diminishes the reliability, reproducibility and eventual translation in day to day management of patients with PCNSL. Here we review established neuroimaging concepts and provide an overview of published literature about novel imaging techniques that may improve diagnosis and response assessments. Finally, we highlight the need for standardization of image acquisition, post-processing, and incorporation of novel imaging biomarkers in early phase PCNSL clinical trials.
Identifiants
pubmed: 35994050
doi: 10.21037/aol-20-53
pmc: PMC9387672
mid: NIHMS1775723
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : NCI NIH HHS
ID : U01 CA220378
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS082609
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA250481
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA221938
Pays : United States
Organisme : NCI NIH HHS
ID : K08 CA237809
Pays : United States
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