Phase I study of intravenous bromodeoxyuridine used concomitantly with radiation therapy in patients with primary malignant brain tumors
The authors report here the results of a Phase I study conducted to determine the toxicity and serum levels that could be tolerated by patients receiving i.v. bromodeoxyuridine (BUdR) concomitantly with radiation therapy. Because of severe thrombocytopenia and leukopenia that was produced in three patients treated by a 96 hour infusion of BUdR at a dose of 1.5 g/m/sup 2//24 hours, the dose was reduced to 0.8 g/m/sup 2//24 hours in these patients and the remaining 9 patients in the study group. Even at this dosage, myelotoxicity was observed. BUdR levels were measured by an isocratic high performance liquid chromatographic (HPLC) method developed for this study. Results of in vitro studies conducted by others suggest that serum levels produced in our patients by administration of doses of 0.6 to 0.8 g/m/sup 2//24 hours should be adequate to achieve a therapeutic effect.
- Research Organization:
- Univ. of California, San Francisco
- OSTI ID:
- 6166468
- Journal Information:
- Int. J. Radiat. Oncol., Biol. Phys.; (United States), Vol. 10:9
- Country of Publication:
- United States
- Language:
- English
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62 RADIOLOGY AND NUCLEAR MEDICINE
BUDR
RADIOSENSITIVITY EFFECTS
LEUKOPENIA
RADIOINDUCTION
RADIOTHERAPY
SIDE EFFECTS
BLOOD PLATELETS
BRAIN
FRACTIONATED IRRADIATION
GLIOMAS
LIQUID COLUMN CHROMATOGRAPHY
PATIENTS
ANTIMETABOLITES
AZINES
BIOLOGICAL MATERIALS
BLOOD
BLOOD CELLS
BODY
BODY FLUIDS
BROMOURACILS
CENTRAL NERVOUS SYSTEM
CHROMATOGRAPHY
DISEASES
DRUGS
HEMIC DISEASES
HETEROCYCLIC COMPOUNDS
HYDROXY COMPOUNDS
IRRADIATION
MATERIALS
MEDICINE
NEOPLASMS
NERVOUS SYSTEM
NUCLEAR MEDICINE
NUCLEOSIDES
NUCLEOTIDES
ORGANIC BROMINE COMPOUNDS
ORGANIC COMPOUNDS
ORGANIC HALOGEN COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANS
PYRIMIDINES
RADIOLOGY
RIBOSIDES
SEPARATION PROCESSES
THERAPY
URACILS
560151* - Radiation Effects on Animals- Man
550603 - Medicine- External Radiation in Therapy- (1980-)