Our purpose was to evaluate an imaging parameter-response relationship between the extent of tumor hypoxia quantified by dynamic F-fluoromisonidazole (F-FMISO) PET/CT and the risk of relapse after radiotherapy in patients with head and neck cancer. Before a prospective cohort of 25 head and neck cancer patients started radiotherapy, they were examined with dynamic F-FMISO PET/CT 0-240 min after tracer injection. F-FMISO image parameters, including a hypoxia metric, derived from pharmacokinetic modeling of dynamic F-FMISO and maximum tumor-to-muscle ratio (TMR) at 4 h after injection, gross tumor volume (GTV), relative hypoxic volume based on and a logistic regression model combining GTV and TMR, were assessed and compared with a previous training cohort ( = 15). Dynamic F-FMISO was used to validate a tumor control probability model based on The prognostic potential with respect to local control of all potential parameters was validated using the concordance index for univariate Cox regression models determined from the training cohort, in addition to Kaplan-Meier analysis including the log-rank test. The tumor control probability model was confirmed, indicating that dynamic F-FMISO allows stratification of patients into different risk groups according to radiotherapy outcome. In this study, was the only parameter that was confirmed as prognostic in the independent validation cohort (concordance index, 0.71; = 0.004). All other investigated parameters, such as TMR, GTV, relative hypoxic volume, and the combination of GTV and TMR, were not able to stratify patient groups according to outcome in this validation cohort ( = not statistically significant). In this study, the relationship between and the risk of relapse was prospectively validated. The data support further evaluation and external validation of dynamic F-FMISO PET/CT as a promising method for patient stratification and hypoxia-based radiotherapy personalization, including dose painting.
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http://dx.doi.org/10.2967/jnumed.119.227744 | DOI Listing |
Clin Transl Imaging
January 2024
Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK; Faculty of Dentistry, Oral & Craniofacial Sciences and School of Cancer & Pharmaceutical Sciences, King's College London, London, United Kingdom.
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.
View Article and Find Full Text PDFNucl Med Biol
November 2023
Department of Oncology, University of Alberta, Cross Cancer Institute, Edmonton T6G 2R7, Alberta, Canada. Electronic address:
Background: Tumour hypoxia is associated with increased metastasis, invasion, poor therapy response and prognosis. Most PET radiotracers developed and used for clinical hypoxia imaging belong to the 2-nitroimidazole family. Recently we have developed novel 2-nitroimidazole-derived PET radiotracer [F]FBNA (N-(4-[F]fluoro-benzyl)-2-(2-nitro-1H-imidazol-1-yl)-acet-amide), an F-labeled analogue of antiparasitic drug benznidazole.
View Article and Find Full Text PDFNucl Med Mol Imaging
February 2023
Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA USA.
Purpose: We evaluated the kinetics of the hypoxia PET radiotracers, [18F]fluoromisonidazole ([18F]FMISO) and [18F]fluoroazomycin-arabinoside ([18F]FAZA), for tumor hypoxia detection and to assess the correlation of hypoxic kinetic parameters with static imaging measures in canine spontaneous tumors.
Methods: Sixteen dogs with spontaneous tumors underwent a 150-min dynamic PET scan using either [18F]FMISO or [18F]FAZA. The maximum tumor-to-muscle ratio (TMR) > 1.
Cancer Chemother Pharmacol
February 2023
Department of Nuclear Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.
The purpose of this study was to investigate the value of tumour-to-muscle (T/M) ratios and Patlak Ki images extracted from whole-body dynamic F-fluoromisonidazole (FMISO) PET/CT Patlak multi-parameter imaging for evaluating the early radiosensitizing effect of oleanolic acid (OA). Twenty-four rats with C6 gliomas were divided into 4 groups and treated with OA (group B), radiotherapy (group C), both (group D) or neither (group A). Whole-body dynamic F-FMISO PET/CT scans were performed for 120 min before treatment and 24 h following the treatment course.
View Article and Find Full Text PDFRadiother Oncol
June 2022
German Cancer Research Center (DKFZ), Heidelberg, Germany; and German Cancer Consortium (DKTK), partner site Tübingen, Germany; Section for Biomedical Physics, Department of Radiation Oncology, University Hospital Tübingen, University of Tübingen, Germany. Electronic address:
Background And Purpose: Tumor hypoxia is a major cause of resistance to radiochemotherapy in locally advanced head-and-neck cancer (LASCCHN). We present results of a randomized phase II trial on hypoxia dose escalation (DE) in LASCCHN based on dynamic [F]FMISO (dynFMISO) positron emission tomography (PET). The purpose was to confirm the prognostic value of hypoxia PET and assess feasibility, toxicity and efficacy of hypoxia-DE.
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