Abstract
Hypoxia is a major risk factor of prostate cancer radioresistance. We evaluated hypoxia non-invasively, using 18F-Misonidazole PET/CT prior to radiotherapy and after a dose of 20 Gy in intermediate-risk prostate cancer patients. Decreased hypoxic volumes were observed in all patients, suggesting that radiotherapy induces early prostate tumor reoxygenation.
Keywords:
Dose painting radiotherapy; FAZA; IMRT; Misonidazole; Radioresistance.
Copyright © 2019 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell Hypoxia / drug effects
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Cell Hypoxia / radiation effects*
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Fluorine Radioisotopes
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Humans
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Male
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Middle Aged
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Misonidazole / administration & dosage
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Oxygen / metabolism
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Positron Emission Tomography Computed Tomography
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Prostatic Neoplasms / diagnostic imaging
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Prostatic Neoplasms / metabolism*
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Prostatic Neoplasms / pathology
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Prostatic Neoplasms / radiotherapy*
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Radiation-Sensitizing Agents / administration & dosage
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Radiopharmaceuticals / administration & dosage
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Radiotherapy, Intensity-Modulated
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Retrospective Studies
Substances
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Fluorine Radioisotopes
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Radiation-Sensitizing Agents
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Radiopharmaceuticals
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Misonidazole
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Fluorine-18
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Oxygen