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Clinical Trial
. 1984 Feb 18;1(8373):359-62.
doi: 10.1016/s0140-6736(84)90411-2.

Methotrexate systemic clearance influences probability of relapse in children with standard-risk acute lymphocytic leukaemia

Clinical Trial

Methotrexate systemic clearance influences probability of relapse in children with standard-risk acute lymphocytic leukaemia

W E Evans et al. Lancet. .

Abstract

108 children with standard-risk acute lymphocytic leukaemia (ALL) were randomised to a post-induction treatment protocol including 15 doses of intermediate-dose methotrexate (1000 mg/m2) in addition to conventional oral therapy of mercaptopurine and low-dose methotrexate. After median follow-up of 26 months, 22 patients have had relapses. Among the 108 patients, rates of methotrexate systemic clearance ranged from 44.7 to 132 ml/min/m2. When the group was divided into three subgroups according to the patients' rates of methotrexate clearance, statistical analysis of the Kaplan-Meier curves estimating the probability of complete remission showed significant differences (p = 0.016) among the subgroups, patients with faster clearance having higher probability of relapse. Multivariate Cox's regression analysis incorporating other potential prognostic variables identified three significant variables influencing the risk of relapse--methotrexate clearance and white-blood-cell count and haemoglobin level at diagnosis (p = 0.0015). This study has demonstrated the potential clinical importance of the rate of drug clearance in children with ALL.

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