Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention
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[Cancer Research 54, 5251-5254, October 15, 1994]
© 1994 American Association for Cancer Research

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Expression of µ Class Glutathione S-Transferase Correlates with Event-free Survival in Childhood Acute Lymphoblastic Leukemia1

Andrew G. Hall2, Pernille Autzen, Alex R. Cattan, Archibald J. Malcolm, Michael Cole, Jennifer Kernahan and Michael M. Reid

Leukaemia Research Fund Remission Unit, 4th Floor, Cookson Building, Medical School, Framlington Place [A. G. H.] and Department of Haematology, Royal Victoria Infirmary [A. R. C., M. M. R., J. K.], Newcastle upon Tyne NE2 4HH; Department of Pathology, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH [P. A., A. J. M.]; and Departments of Child Health and Medical Statistics [M. C.], Newcastle upon Tyne, NE2 4HH United Kingdom

Expression of the main classes ({pi}, µ, and {alpha}) of glutathione S-transferase (GST) was assessed in the blasts of children presenting with acute lymphoblastic leukemia using an immunohistochemical technique. Bone marrow trephine biopsies obtained at presentation from 71 cases were studied (42 boys, 29 girls; age range, 6 months-14 years; median age, 4 years) and expression was correlated with event-free survival. The period of follow-up was 12–108 months, during which time 21 patients (30%) relapsed. All the samples examined were negative for {alpha} class GST. Samples from 8 patients, all of whom remained in remission at the time of analysis, were found to be negative for {pi} class GST at presentation. Samples from 44 (patients were negative for µ class GST (62%); of these, 36 patients (82%) remained in remission. In comparison, of the 27 patients who were positive for µ class GST, only 14 (52%) remained in remission. Analysis of event-free survival demonstrated that expression of µ class GST predicts a 3-fold increased risk of relapse (95% confidence interval, 1.25–7.26). This risk factor appears to be independent of other recognized prognostic factors.

1 This work was supported by the Leukaemia Research Fund and the Tyneside Leukaemia Research Association.

2 To whom requests for reprints should be addressed.

Received 6/ 9/94. Accepted 8/31/94.




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Copyright © 1994 by the American Association for Cancer Research.