The goal of this study was to compare the value of contrast-enhanced MRI and O-(2-[F]fluoroethyl)-l-tyrosine (F-FET) PET for response assessment in glioma patients after adjuvant temozolomide chemotherapy (TMZ). After biopsy or resection and completion of radiotherapy with concomitant TMZ, 41 newly diagnosed and histomolecularly characterized glioma patients (glioblastoma, 90%; age range, 20-79 y) were subsequently treated with adjuvant TMZ. MR and F-FET PET imaging were performed at baseline and after the second cycle of adjuvant TMZ. We obtained F-FET metabolic tumor volumes (MTVs) as well as mean and maximum tumor-to-brain ratios (TBR and TBR, respectively). Threshold values of F-FET PET parameters to predict outcome were established by receiver-operating-characteristic analyses using a median progression-free survival (PFS) of ≥ 9 mo and overall survival (OS) of ≥ 15 mo as reference. MRI response assessment was based on the Response Assessment in Neuro-Oncology (RANO) working group criteria. The predictive value of changes of F-FET PET and MRI parameters on survival was evaluated subsequently using univariate and multivariate survival estimates. After 2 cycles of adjuvant TMZ chemotherapy, a treatment-induced reduction of MTV and TBR predicted a significantly longer PFS and OS (both ≤ 0.03; univariate survival analyses) whereas RANO criteria were not significant ( > 0.05). Multivariate survival analysis revealed that TBR changes predicted a prolonged PFS ( = 0.012) and changes of MTV a prolonged OS ( = 0.005) independent of O-methylguanine-DNA-methyltransferase promoter methylation and other strong prognostic factors. Changes of F-FET PET parameters appear to be helpful for identifying responders to adjuvant TMZ early after treatment initiation.
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http://dx.doi.org/10.2967/jnumed.120.254243 | DOI Listing |
Zh Vopr Neirokhir Im N N Burdenko
December 2024
Burdenko Neurosurgical Center, Moscow, Russia.
Unlabelled: The development of new drugs in nuclear medicine for diagnosis or treatment (chemotherapy) of brain tumors, in particular gliomas, is inextricably linked with the use of tumor models in animals (usually rats).
Objective: To compare the widely used glioma cell model C6 and the new experimental tissue model of glioblastoma 101.8.
Neurooncol Adv
November 2024
Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark.
Background: Magnetic resonance imaging (MRI) cerebral blood volume (CBV) measurements improve the diagnosis of recurrent gliomas. The study investigated the prognostic value of dynamic contrast-enhanced (DCE) CBV imaging in treated IDH wildtype glioblastoma when added to MRI or amino acid positron emission tomography (PET).
Methods: Hybrid [F]FET PET/MRI with 2CXM (2-compartment exchange model) DCE from 86 adult patients with suspected recurrent or residual glioblastoma were retrospectively analyzed.
Neurooncol Adv
October 2024
Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark.
Background: In the present study, early response assessment by o-(2-[F]fluoroethyl)-l-tyrosine (FET) positron emission tomography (PET) and contrast-enhanced magnetic resonance imaging (MRI) were investigated in a phase II open-label single-center study of nivolumab plus bevacizumab for recurrent high-grade astrocytic glioma.
Methods: Twenty patients with nonresectable first recurrence of high-grade astrocytic glioma after EORTC/NCIC protocol underwent [F]FET PET/MRI at baseline and after 2 cycles of treatment. Whole brain values of contrast-enhancing volume on MRI (CEV), of the mean (TBR) and maximal tumor-to-background ratio (TBR), and of metabolically active volume (MTV) on [F]FET PET were obtained.
Ann Nucl Med
November 2024
Department of Nuclear Medicine, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, 970423, Taiwan.
Neuroradiology
November 2024
Medical Cyclotron Facility, Board of Radiation and Isotope Technology (BRIT), Bhabha Atomic Research Center, Mumbai, India.
Purpose: The clinico-radiological dilemma in post-treatment high-grade gliomas, between disease recurrence (TR) and treatment-related changes (TRC), still persists. FET (Fluoro-ethyl-tyrosine) PET has been extensively used as problem-solving modality for cases where MR imaging is inconclusive. We incorporated a systematic imaging and clinical follow-up algorithm in a multi-disciplinary clinic (MDC) setting to analyse our cohort of FET PET in post-treatment gliomas.
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