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Purpose: Hypoxia is a major cause of radioresistance in head and neck cancer (HNC), resulting in treatment failure and disease recurrence. F-fluoromisonidazole [F]FMISO PET has been proposed as a means of localising intratumoural hypoxia in HNC so that radiotherapy can be specifically escalated in hypoxic regions. This concept may not be deliverable in routine clinical practice, however, given that [F]FMISO PET is costly, time consuming and difficult to access. The aim of this review was to summarise clinical studies involving [F]FMISO PET to ascertain whether it can be used to guide radiotherapy treatment in HNC.
Methods: A comprehensive literature search was conducted on PubMed and Web of Science databases. Studies investigating [F]FMISO PET in newly diagnosed HNC patients were considered eligible for review.
Results: We found the following important results from our literature review: 1)Studies have focussed on comparing [F]FMISO PET to other hypoxia biomarkers, but currently there is no evidence of a strong correlation between [F]FMISO and these biomarkers.2)The results of [F]FMISO PET imaging are not necessarily repeatable, and the location of uptake may vary during treatment.3)Tumour recurrences do not always occur within the pretreatment hypoxic volume on [F]FMISO PET.4)Dose modification studies using [F]FMISO PET are in a pilot phase and so far, none have demonstrated the efficacy of radiotherapy dose painting according to [F]FMISO uptake on PET.
Conclusions: Our results suggest it is unlikely [F]FMISO PET will be suitable for radiotherapy dose adaptation in HNC in a routine clinical setting. Part of the problem is that hypoxia is a dynamic phenomenon, and thus difficult to delineate on a single scan. Currently, it is anticipated that [F]FMISO PET will remain useful within the research setting only.
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http://dx.doi.org/10.1007/s40336-023-00607-y | DOI Listing |
J Labelled Comp Radiopharm
September 2025
State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Research, Investigation and Evaluation of Radiopharmaceuticals, NMPA Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Departmen
A peptide-based, hypoxia-inducible factor-1 α (HIF-1α) specific PET tracer for tumor hypoxia imaging is reported. It was prepared with a rapid AlF labeling method with high stability. AlF-CLLFVY specifically binds to HIF-1α with high affinity and shows higher uptake in cells under hypoxia.
View Article and Find Full Text PDFJ Comput Aided Mol Des
September 2025
Department of Medical Physics and Biomedical Nanotechnologies, V.N. Karazin Kharkiv National University, 4 Svobody Sq., Kharkiv, 61022, Ukraine.
Fluorine-18-labeled radiopharmaceuticals are central to PET-based oncology imaging, yet comparative evaluations of their mechanistic behavior and diagnostic potential remain fragmented. In this study, we present a multidimensional in silico framework integrating pharmacokinetic modeling, structural ADMET prediction, and unsupervised clustering to systematically evaluate five widely used F-labeled PET radiopharmaceuticals: [F]FDG, [F]FET, [F]DOPA, [F]FMISO, and [F]FLT. Each radiopharmaceutical was simulated using a harmonized three-compartment model in COPASI to capture uptake dynamics under both normal and pathological conditions.
View Article and Find Full Text PDFAsia Ocean J Nucl Med Biol
January 2025
Faculty of Medicine and Health, University of Sydney, Camperdown, Australia and Department of Medical Oncology, Royal North Shore Hospital, St Leonards, Australia.
Objectives: The phenomenon of peripheral [Ga]DOTATATE avidity without central avidity (which we have termed a "DONUT") has been observed in neuroendocrine neoplasm (NEN) lesions. There has been speculation as to whether this is due to hypoxia, de-differentiated disease or other causes. The presence of hypoxia may have prognostic and therapeutic implications, and was evaluated in these lesions using the PET hypoxia imaging biomarker [F]FMISO.
View Article and Find Full Text PDFPhys Imaging Radiat Oncol
April 2025
Department of Medical Physics, Memorial Sloan Kettering Cancer Center New York, 321 East 61st Street, NY 10065, USA.
Background And Purpose: Tumor hypoxia is linked to lower local control rates and increased distant disease progression during head and neck (HN) radiotherapy. F-fluoromisonidazole (F-FMISO) positron emission tomography (PET) imaging measured hypoxia can aid dose selection for HN patients, but its availability is limited. Hence, we tested the hypothesis that an artificial intelligence (AI) model could synthesize F-FMISO-like images from routinely acquired F-fluorodeoxyglucose (F-FDG) PET images in order to predict primary tumor or metastatic lymph node hypoxic volumes.
View Article and Find Full Text PDFClin Nucl Med
July 2025
Department of Radiology, Ankara University Medical School, Ankara, Turkey.
Background: Transarterial radioembolization (TARE) is a therapeutic option for patients with liver tumors. However, factors responsible for treatment resistance in TARE remain largely unknown. In this study, we aimed to investigate the role of hypoxia in the treatment response of liver tumors using 18 F-FMISO PET imaging before TARE.
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