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Glucose Uptake by Gliomas After TreatmentA Positron Emission Tomographic Study
Jack M. Rozental, MD, PhD;
Ross L. Levine, MD;
Robert J. Nickles, PhD;
Jeffrey A. Dobkin, MD
Arch Neurol. 1989;46(12):1302-1307.
Abstract
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Positron emission tomographic scanning with fludeoxyglucose F 18 (18F-fluorodeoxyglucose) was used to study acute changes in gliomas after chemotherapy. In six experimental subjects, scans were obtained before and at days 1, 7, and 30 after treatment. Five control patients with gliomas who did not undergo chemotherapy had two scans, 1 month apart. Ratios were calculated between peak tumor regional cerebral metabolic rate for glucose and contralateral white matter. The percent change in ratios relative to each patient's baseline scan was calculated. Ratios in three stable controls remained unchanged over the study interval; in two controls it increased 155% and 36% and both died of tumor progression. In experimental subjects, ratios increased 20% to 100% 24 hours after chemotherapy and then decreased until at 28 days they varied between 22% above and 35% below baseline. The increased fludeoxyglucose F 18 uptake at 24 hours could be from uncoupling oxidative phosphorylation or shunting glucose to ribose phosphates for salvage nucleoside synthesis.
Author Affiliations
From the Neurology and Research Services (Drs Rozental and Levine) and the Division of Nuclear Medicine (Dr Dobkin), William S. Middleton Memorial Veterans Administration (VA) Hospital, Madison, Wis; and the Departments of Neurology (Drs Rozental and Levine), Neurosurgery (Dr Rozental), Radiology (Dr Levine), and Medical Physics (Dr Nickles), University of Wisconsin Medical School, Madison.
Footnotes
Accepted for publication May 22, 1989.
Reprint requests to Neurology Service, William S. Middleton Memorial VA Hospital, 2500 Overlook Terr, Madison, WI 53705 (Dr Rozental).
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