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[Cancer Research 49, 4363-4368, August 1, 1989]
© 1989 American Association for Cancer Research

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In Vitro and in Vivo Killing of Acute Lymphoblastic Leukemia Cells by L-Asparaginase1

Barbara L. Asselin2, Daniel Ryan, Christopher N. Frantz, Samuel D. Bernal, Pearl Leavitt, Stephen E. Sallan and Harvey J. Cohen

Departments of Pediatrics [B. L. A., C. N. F., H. J. C.] and Pathology [D. R.], University of Rochester School of Medicine and Dentistry, Rochester, New York 14642 and Departments of Pediatrics [S. E. S.] and Medicine [S. D. B., P. L.], Dana-Farber Cancer Institute, Boston, Massachusetts 02115

L-Asparaginase (ASNase) is a potent antileukemic enzyme routinely used in the treatment of children with acute lymphoblastic leukemia. As part of investigations of the biological activity of ASNase, we have developed techniques which measure the in vitro and in vivo cell killing ability of ASNase. To study the effect of ASNase on in vitro survival of primary lymphoblasts, bone marrow mononuclear cells obtained from untreated patients with acute lymphoblastic leukemia were cultured with and without ASNase. After 5 days, viable cells were counted using trypan blue exclusion to calculate total cell kill due to ASNase. Propidium iodide exclusion, leukemia cell surface antigens, and flow cytometry were used to determine leukemia cell kill due to ASNase. Comparison of leukemia cell kill and total cell kill showed a direct linear relationship (n = 24, r = 0.7), preferential killing of leukemia cells by ASNase (slope = 0.66), and that use of leukemia cell surface markers yielded a more accurate measurement of leukemia cell killing. ASNase at concentrations from 0.0001 to 0.1 IU/ml had equal effects on extent of leukemia cell killing (P = 0.3 to 0.7), suggesting the absence of a dose response at the ASNase concentrations tested. As a measure of the in vivo response to ASNase treatment, the number of viable bone marrow leukemia cells in the patient prior to and 5 days after treatment with ASNase was measured as the product of (% of rhodamine 123 fluorescent [viable] cells) x (absolute leukemic infiltrate). The change which occurred in the viable leukemic infiltrate was the same for patients whether they received 25,000 or 2,500 IU/m2 of ASNase as a single drug. There was a linear correlation (n = 8, r = 0.9) between in vivo and in vitro leukemia cell killing by ASNase. Thus, the in vitro assay described here can be used to predict in vivo sensitivity to ASNase in acute lymphoblastic leukemia.

1 Supported by Program Project Grant 5P01CA34183-06 from the NIH, FDA Grant 000199-03, USPHS Training Grant HL 07152 (B. L. A.), and Wilmot Cancer Research Fellowship awarded by the James T. Wilmot Foundation (B. L. A.).

2 To whom requests for reprints should be addressed, at Department of Pediatrics, Box 777, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, NY 14642.

Received 12/28/88. Revised 4/27/89. Accepted 5/ 4/89.




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Copyright © 1989 by the American Association for Cancer Research.