A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML

Abstract. The proportion of patients with acute myeloid leukemia (AML) cured is increased by administering high-dose cytarabine (HiDAC). It remains uncertain whether to administer HiDAC as induction or consolidation, and whether ≥1 cycle of HiDAC is required. Our retrospective study of 416 adult AML...

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Main Authors: Anthony P. Schwarer, Jason Butler, Kathryn Jackson, Ashanka Beligaswatte, Louisa Martin, Glen Kennedy, Zantomio Daniela, Ian Lewis, Devendra Hiwase, Joel Wight, Simon He, Andrew Grigg, Kirk Morris, Peter Mollee, Paula Marlton
Format: Article
Language:English
Published: Wiley 2018-12-01
Series:HemaSphere
Online Access:http://journals.lww.com/10.1097/HS9.0000000000000158
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author Anthony P. Schwarer
Jason Butler
Kathryn Jackson
Ashanka Beligaswatte
Louisa Martin
Glen Kennedy
Zantomio Daniela
Ian Lewis
Devendra Hiwase
Joel Wight
Simon He
Andrew Grigg
Kirk Morris
Peter Mollee
Paula Marlton
author_facet Anthony P. Schwarer
Jason Butler
Kathryn Jackson
Ashanka Beligaswatte
Louisa Martin
Glen Kennedy
Zantomio Daniela
Ian Lewis
Devendra Hiwase
Joel Wight
Simon He
Andrew Grigg
Kirk Morris
Peter Mollee
Paula Marlton
author_sort Anthony P. Schwarer
collection DOAJ
description Abstract. The proportion of patients with acute myeloid leukemia (AML) cured is increased by administering high-dose cytarabine (HiDAC). It remains uncertain whether to administer HiDAC as induction or consolidation, and whether ≥1 cycle of HiDAC is required. Our retrospective study of 416 adult AML patients, excluding good risk cytogenetics, compared a single cycle of HiDAC-based therapy followed by 2 cycles of standard-dose cytarabine (SDAC) (HiDAC induction cohort) with SDAC-based chemotherapy followed by 2 cycles of HiDAC-based chemotherapy (HiDAC consolidation cohort). Complete remission (CR) rate was greater in the HiDAC induction cohort (90% vs 78%, P < 0.01) which did not lead to an improved overall survival (48% vs 43%, P = 0.18) or disease-free survival (DFS) (39% vs 45%, P = 0.95). We noted that, after censoring for allogeneic hematopoetic stem cell transplant (alloHSCT) in CR1, the cumulative incidence of relapse was lower in the HiDAC consolidation cohort in patients with intermediate risk cytogenetics (68% vs 44%, P = 0.01), which lead to a greater DFS (30% vs 47%, P = 0.095). In the patients with adverse risk cytogenetics, the RR was numerically greater in the HiDAC consolidation cohort (52% vs 80%, P = 0.60) which lead to a lower DFS (27% vs 4%, P = 0.11). Our data show that, although the HiDAC induction cohort (1 cycle of HiDAC) achieved a greater CR rate, there were no overall survival differences between the 2 cohorts, and that the HiDAC consolidation cohort (2 cycles of HiDAC) had a lower RR and greater DFS in those patients with intermediate risk cytogenetics who did not undergo alloHSCT in CR1.
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spelling doaj.art-a833d18f98a24370b143cc52f3a42cf32024-03-03T00:26:18ZengWileyHemaSphere2572-92412018-12-012610.1097/HS9.0000000000000158201812000-00008A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AMLAnthony P. SchwarerJason ButlerKathryn JacksonAshanka BeligaswatteLouisa MartinGlen KennedyZantomio DanielaIan LewisDevendra HiwaseJoel WightSimon HeAndrew GriggKirk MorrisPeter MolleePaula MarltonAbstract. The proportion of patients with acute myeloid leukemia (AML) cured is increased by administering high-dose cytarabine (HiDAC). It remains uncertain whether to administer HiDAC as induction or consolidation, and whether ≥1 cycle of HiDAC is required. Our retrospective study of 416 adult AML patients, excluding good risk cytogenetics, compared a single cycle of HiDAC-based therapy followed by 2 cycles of standard-dose cytarabine (SDAC) (HiDAC induction cohort) with SDAC-based chemotherapy followed by 2 cycles of HiDAC-based chemotherapy (HiDAC consolidation cohort). Complete remission (CR) rate was greater in the HiDAC induction cohort (90% vs 78%, P < 0.01) which did not lead to an improved overall survival (48% vs 43%, P = 0.18) or disease-free survival (DFS) (39% vs 45%, P = 0.95). We noted that, after censoring for allogeneic hematopoetic stem cell transplant (alloHSCT) in CR1, the cumulative incidence of relapse was lower in the HiDAC consolidation cohort in patients with intermediate risk cytogenetics (68% vs 44%, P = 0.01), which lead to a greater DFS (30% vs 47%, P = 0.095). In the patients with adverse risk cytogenetics, the RR was numerically greater in the HiDAC consolidation cohort (52% vs 80%, P = 0.60) which lead to a lower DFS (27% vs 4%, P = 0.11). Our data show that, although the HiDAC induction cohort (1 cycle of HiDAC) achieved a greater CR rate, there were no overall survival differences between the 2 cohorts, and that the HiDAC consolidation cohort (2 cycles of HiDAC) had a lower RR and greater DFS in those patients with intermediate risk cytogenetics who did not undergo alloHSCT in CR1.http://journals.lww.com/10.1097/HS9.0000000000000158
spellingShingle Anthony P. Schwarer
Jason Butler
Kathryn Jackson
Ashanka Beligaswatte
Louisa Martin
Glen Kennedy
Zantomio Daniela
Ian Lewis
Devendra Hiwase
Joel Wight
Simon He
Andrew Grigg
Kirk Morris
Peter Mollee
Paula Marlton
A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
HemaSphere
title A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
title_full A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
title_fullStr A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
title_full_unstemmed A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
title_short A Comparison of High-Dose Cytarabine During Induction Versus Consolidation Therapy in Newly Diagnosed AML
title_sort comparison of high dose cytarabine during induction versus consolidation therapy in newly diagnosed aml
url http://journals.lww.com/10.1097/HS9.0000000000000158
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