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[Cancer Research 52, 719-725, February 1, 1992]
© 1992 American Association for Cancer Research

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Measurement of Thymidine Replacement in Patients with High Grade Gliomas, Head and Neck Tumors, and High Grade Sarcomas after Continuous Intravenous Infusions of 5-Iododeoxyuridine

John A. Cook, Joseph Glass, Robert Lebovics, Hunt Bobo, Harvey Pass, Thomas F. DeLaney, Edward H. Oldfield, James B. Mitchell, Eli Glatstein and Thomas E. Goffman1

Radiation Oncology [J.A.C., J.G., T.F.D., J.B.M., E.G., T.E.G.], Surgical Neurology [R.L.], and Thoracic Surgery [H.P.] Branches, National Cancer Institute, and Otolaryngology Branch [H.B., E.H.O.], National Institute for Deafness, NIH, Bethesda, Maryland 20892

Based upon the radiation sensitization properties of the halogenated pyrimidines, 5-iododeoxyuridine (IdUrd) and 5-bromodeoxyuridine, long term i.v. infusions of halogenated pyrimidines in conjunction with fractionated radiation therapy have been evaluated in the treatment of a variety of human malignancies. While clinical studies have attempted to measure the halogenated pyrimidine incorporation, few have successfully related tumor response to the incorporation of IdUrd by the tumor. The present study reports the continuous IdUrd labeling index (number of cells labeled) and the IdUrd corrected replacement (percentage of thymidine replacement in the labeled cells of the population) from the tumors of 17 patients who received continuous infusions of IdUrd (1000 mg/m2/24 h). The tumors treated included four high grade gliomas, five head and neck tumors, four high grade sarcomas, and five other tumors of varying types. Less than 25% of the cells in three of four gliomas incorporated IdUrd after 5–7-day IdUrd infusion time. Corrected replacement for the gliomas ranged from 0 to 4%. In contrast, 63–85% of the cells in the head and neck biopsies were labeled with IdUrd after 3–7-day IdUrd infusions suggesting that these large tumors (3–12 cm diameter) have a high fraction of dividing cells. Corrected replacements values for the head and neck tumor patients ranged from 2.9 to 26.3%. The high grade sarcomas also demonstrated a high percentage of IdUrd labeled cells (57–79%) with three patients having corrected replacements of 7.5–14.2%. The continuous labeling and thymidine replacement data for four patients from whom serial biopsies were taken during IdUrd infusion demonstrated both an increasing IdUrd replacement and continuous labeling index with an increasing duration of IdUrd infusion. The clinical response of both the high grade glioma and head and neck tumor patients indicate that the IdUrd replacement and labeling data may provide some important predictive information with regard to the successful use of the halogenated pyrimidines in clinical radiation trials.

1 To whom requests for reprints should be addressed, at Radiation Oncology Branch/NCI, Bldg. 10, Room B3-B69, Bethesda, MD 20892.

Received 7/16/91. Accepted 11/13/91.




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A. Doiron, D. T. T. Yapp, M. Olivares, J. X. X. Zhu, and S. Lehnert
Tumor Radiosensitization by Sustained Intratumoral Release of Bromodeoxyuridine
Cancer Res., August 1, 1999; 59(15): 3677 - 3681.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1992 by the American Association for Cancer Research.