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Article: A hybrid [18F]fluoropivalate PET-multiparametric MRI to detect and characterise brain tumour metastases based on a permissive environment for monocarboxylate transport

TitleA hybrid [18F]fluoropivalate PET-multiparametric MRI to detect and characterise brain tumour metastases based on a permissive environment for monocarboxylate transport
Authors
KeywordsContrast-enhanced magnetic resonance imaging
Intracranial metastatic disease
Metabolomics
Positron emission tomography
Stereotactic radiosurgery
[18F]fluoropivalate
Issue Date1-Jan-2025
PublisherSpringer
Citation
European Journal of Nuclear Medicine and Molecular Imaging, 2025 How to Cite?
AbstractThe incidence of Intracranial Metastatic Disease (IMD) continues to increase in part due to improvements in systemic therapy resulting in durable control of extra-cranial disease (ECD). Contrast-enhanced Magnetic Resonance Imaging (CE-MRI) is the preferred method for imaging IMD, but has limitations particularly in follow-up surveillance scans to optimise patient care. We investigate a new diagnostic approach of hybrid ([18]F]fluoropivalate (FPIA) Positron Emission Tomography-multiparametric MRI (PET-mpMRI), in 12 treatment-naïve and 10 stereotactic radiosurgery (SRS)-treated patients (± combination therapy within 4–8 weeks). High FPIA uptake was seen in all IMD compared to contralateral white matter, regardless of ECD tumour-of-origin (p = 0.0001) and FPIA-PET volumes extended beyond CE-MRI volumes in treatment-naïve but not SRS-treated tumours. Patients with maximum PET Standardised Uptake Value, (SUVmax) ≥ 2.0 showed particularly short overall-survival (median 4 v 15 months, p = 0.0136), while CE-MRI was uninformative regarding outcome; a PET-mpMRI grade-measure also provided non-invasive prediction of overall-survival, warranting larger studies of PET-mpMRI. Independent metabolomics analyses were consistent with shared adaptation of IMD to utilise or accumulate monocarboxylates and acylcarnitines, respectively, providing a common phenotypic basis to FPIA-PET. Reprogrammed monocarboxylate metabolism-related FPIA-PET provides new insights into annotating IMD, to be expounded in future opportunities for therapy decisions for the growing number of cancer patients with IMD [Trial registration reference: Clinicaltrials.gov NCT04807582; 3rd November 2021, retrospectively registered].
Persistent Identifierhttp://hdl.handle.net/10722/355726
ISSN
2023 Impact Factor: 8.6
2023 SCImago Journal Rankings: 2.280
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorIslam, S.-
dc.contributor.authorInglese, M.-
dc.contributor.authorAravind, P.-
dc.contributor.authorBarwick, T. D.-
dc.contributor.authorMauri, F.-
dc.contributor.authorMcLeavy, L.-
dc.contributor.authorÅrstad, E.-
dc.contributor.authorWang, J.-
dc.contributor.authorPuccio, I.-
dc.contributor.authorHung, L.-
dc.contributor.authorLu, H.-
dc.contributor.authorO’Neill, K.-
dc.contributor.authorWaldman, A. D.-
dc.contributor.authorWilliams, M.-
dc.contributor.authorAboagye, E. O.-
dc.date.accessioned2025-05-06T00:35:06Z-
dc.date.available2025-05-06T00:35:06Z-
dc.date.issued2025-01-01-
dc.identifier.citationEuropean Journal of Nuclear Medicine and Molecular Imaging, 2025-
dc.identifier.issn1619-7070-
dc.identifier.urihttp://hdl.handle.net/10722/355726-
dc.description.abstractThe incidence of Intracranial Metastatic Disease (IMD) continues to increase in part due to improvements in systemic therapy resulting in durable control of extra-cranial disease (ECD). Contrast-enhanced Magnetic Resonance Imaging (CE-MRI) is the preferred method for imaging IMD, but has limitations particularly in follow-up surveillance scans to optimise patient care. We investigate a new diagnostic approach of hybrid ([18]F]fluoropivalate (FPIA) Positron Emission Tomography-multiparametric MRI (PET-mpMRI), in 12 treatment-naïve and 10 stereotactic radiosurgery (SRS)-treated patients (± combination therapy within 4–8 weeks). High FPIA uptake was seen in all IMD compared to contralateral white matter, regardless of ECD tumour-of-origin (p = 0.0001) and FPIA-PET volumes extended beyond CE-MRI volumes in treatment-naïve but not SRS-treated tumours. Patients with maximum PET Standardised Uptake Value, (SUVmax) ≥ 2.0 showed particularly short overall-survival (median 4 v 15 months, p = 0.0136), while CE-MRI was uninformative regarding outcome; a PET-mpMRI grade-measure also provided non-invasive prediction of overall-survival, warranting larger studies of PET-mpMRI. Independent metabolomics analyses were consistent with shared adaptation of IMD to utilise or accumulate monocarboxylates and acylcarnitines, respectively, providing a common phenotypic basis to FPIA-PET. Reprogrammed monocarboxylate metabolism-related FPIA-PET provides new insights into annotating IMD, to be expounded in future opportunities for therapy decisions for the growing number of cancer patients with IMD [Trial registration reference: Clinicaltrials.gov NCT04807582; 3rd November 2021, retrospectively registered].-
dc.languageeng-
dc.publisherSpringer-
dc.relation.ispartofEuropean Journal of Nuclear Medicine and Molecular Imaging-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectContrast-enhanced magnetic resonance imaging-
dc.subjectIntracranial metastatic disease-
dc.subjectMetabolomics-
dc.subjectPositron emission tomography-
dc.subjectStereotactic radiosurgery-
dc.subject[18F]fluoropivalate-
dc.titleA hybrid [18F]fluoropivalate PET-multiparametric MRI to detect and characterise brain tumour metastases based on a permissive environment for monocarboxylate transport-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1007/s00259-025-07118-0-
dc.identifier.scopuseid_2-s2.0-85218008262-
dc.identifier.eissn1619-7089-
dc.identifier.isiWOS:001415642700001-
dc.identifier.issnl1619-7070-

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