Please use this identifier to cite or link to this item: https://hdl.handle.net/1/1031
Title: Idarubicin dose escalation during consolidation therapy for adult Acute Myeloid Leukemia
Authors: Tiley, Campbell ;Bradstock, K.F.;Link, E.;Di Iulio, J.;Szer, J.;Marlton, P.;Wei, A.H.;Enno, A.;Schwarer, A.;Lewis, I.D.;D'Rozario, J.;Coyle, L.;Cull, G.;Campbell, P.;Leahy, M.F.;Hahn, U.;Cannell, P.;Lowenthal, R.M.;Moore, J.;Cartwright, K.;Cunningham, I.;Taper, J.;Grigg, A.;Roberts, A.W.;Benson, W.;Hertzberg, M.;Deveridge, S.;Rowlings, P.;Mills, A.K.;Gill, Devinder S ;Bardy, P.;Campbell, L.J.;Seymour, J.F.
Affliation: Central Coast Local Health District
Gosford Hospital
Issue Date: May-2017
Source: 35(15):1678-1685
Journal title: Journal of Clinical Oncology
Department: Haematology
Abstract: Purpose Higher doses of the anthracycline daunorubicin during induction therapy for acute myeloid leukemia (AML) have been shown to improve remission rates and survival. We hypothesized that improvements in outcomes in adult AML may be further achieved by increased anthracycline dose during consolidation therapy. Patients and Methods Patients with AML in complete remission after induction therapy were randomly assigned to receive two cycles of consolidation therapy with cytarabine 100 mg/m2 daily for 5 days, etoposide 75 mg/m2 daily for 5 days, and idarubicin 9 mg/m2 daily for either 2 or 3 days (standard and intensive arms, respectively). The primary end point was leukemia-free survival (LFS). Results Two hundred ninety-three patients 16 to 60 years of age, excluding those with core binding factor AML and acute promyelocytic leukemia, were randomly assigned to treatment groups (146 to the standard arm and 147 to the intensive arm). Both groups were balanced for age, karyotypic risk, and FLT3-internal tandem duplication and NPM1 gene mutations. One hundred twenty patients in the standard arm (82%) and 95 patients in the intensive arm (65%) completed planned consolidation ( P < .001). Durations of severe neutropenia and thrombocytopenia were prolonged in the intensive arm, but there were no differences in serious nonhematological toxicities. With a median follow-up of 5.3 years (range, 0.6 to 9.9 years), there was a statistically significant improvement in LFS in the intensive arm compared with the standard arm (3-year LFS, 47% [95% CI, 40% to 56%] v 35% [95% CI, 28% to 44%]; P = .045). At 5 years, the overall survival rate was 57% in the intensive arm and 47% in the standard arm ( P = .092). There was no evidence of selective benefit of intensive consolidation within the cytogenetic or FLT3-internal tandem duplication and NPM1 gene mutation subgroups. Conclusion An increased cumulative dose of idarubicin during consolidation therapy for adult AML resulted in improved LFS, without increased nonhematologic toxicity.
URI: https://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/1031
DOI: 10.1200/JCO.2016.70.6374
Pubmed: https://www.ncbi.nlm.nih.gov/pubmed/28368672
ISSN: 0732-183x
Publicaton type: Journal Article
Keywords: Leukaemia
Leukemia
Cancer
Study or Trial: Clinical Trial
Appears in Collections:Oncology / Cancer

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