The Effect of 6-Mercaptopurine on the Duration of Steroid-induced Remissions in Acute Leukemia: A Model for Evaluation of Other Potentially Useful Therapy

ACUTE LEUKEMIA GROUP B(National Institutes of Health), Emil J. Freireich(National Institutes of Health), Edmund A. Gehan(National Institutes of Health), Emil Frei(National Institutes of Health), LESLIE R. SCHROEDER(Children's Hospital of Philadelphia), Irving J. Wolman(Children's Hospital of Philadelphia), RACHAD ANBARI(Children's Hospital of Philadelphia), E. OMAR BURGERT(Mayo Clinic in Arizona), Stephen D. Mills(Roswell Park Comprehensive Cancer Center), Donald Pinkel(Roswell Park Comprehensive Cancer Center), Oleg S. Selawry(Roswell Park Comprehensive Cancer Center), John H. Moon(Emory University), Benjamin R. Gendel(Emory University), Charles L. Spurr(Dartmouth–Hitchcock Medical Center), R. Storrs(Dartmouth–Hitchcock Medical Center), Farid I. Haurani(Mount Sinai Hospital), Barth Hoogstraten(Maimonides Medical Center), Stanley Chun-Wei Lee(Maimonides Medical Center)
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Abstract

Abstract The effect of 6-MP therapy on the duration of remissions induced by adrenal corticosteroids has been studied as a model for testing of new agents. Ninetytwo patients under age 20 entered the study and were accepted for analysis. Sixty-two (67 per cent) had complete or partial remissions induced by corticosteroids. Patients in remission were randomly assigned to maintenance therapy with either 6-MP or placebo. The median duration of 6-MP-maintained complete remissions was 33 weeks and for placebo, 9 weeks. A sequential experimental design was used to analyze remission times while the study was in progress. This resulted in the study being stopped after analysis of the remission times of 21 pairs of patients (42 patients). Overall survival was not significantly different for the two treatment programs, since patients maintained on placebo were treated with 6-MP when relapse occurred. The activity of the known active antileukemic compound 6-MP was readily detected by this experimental design without compromise of optimal survival. Such a design should prove useful for the evaluation of new agents and also permit study of the remission maintenance activity of a compound separately from its remission inducing activity.


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