Abstract
Glioma is the most common malignant brain tumor. Hypoxia is closely related to the malignancy of gliomas, and positron emission tomography (PET) can noninvasively visualize the degree and the expansion of hypoxia. Currently,18 F-fluoromisonidazole (FMISO) is the most common radiotracer for hypoxia imaging. The clinical usefulness of FMISO PET has been established; it can distinguish glioblastomas from lower-grade gliomas and can predict the microenvironment of a tumor, including necrosis, vascularization, and permeability. FMISO PET provides prognostic information, including survival and treatment response information. Because hypoxia decreases a tumor’s sensitivity to radiation therapy, dose escalation to an FMISO-positive volume is an attractive strategy. Although this idea is not new, an insufficient amount of evidence has been obtained regarding this concept. New tracers for hypoxia imaging such as18 F-DiFA are being tested. In the future, hypoxia imaging will play an important role in glioma management.
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Hirata, K., Yamaguchi, S., Shiga, T., Kuge, Y., & Tamaki, N. (2019, August 1). The roles of hypoxia imaging using18 f-fluoromisonidazole positron emission tomography in glioma treatment. Journal of Clinical Medicine. MDPI. https://doi.org/10.3390/jcm8081088
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