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Comparison of high-dose cytarabine and timed-sequential chemotherapy as consolidation for younger adults with AML in first remission: the ALFA-9802 study.

Authors :
Thomas, Xavier
Elhamri, Mohamed
Raffoux, Emmanuel
Renneville, Aline
Pautas, Cécile
de Botton, Stéphane
de Revel, Thierry
Reman, Oumedaly
Terré, Christine
Gardin, Claude
Chelghoum, Youcef
Boissel, Nicolas
Quesnel, Bruno
Hicheri, Yosr
Bourhis, Jean-Henri
Fenaux, Pierre
Preudhomme, Claude
Michallet, Mauricette
Castaigne, Sylvie
Dombret, Hervé
Source :
Blood. 8/18/2011, Vol. 118 Issue 7, p1754-1762. 9p.
Publication Year :
2011

Abstract

To assess the value of administering timed-sequential chemotherapy (TSC; 2 therapeutic sequences separated by a 4-day interval-free chemotherapy) or high-dose cytarabine (HDAraC) cycles in consolidation therapy for acute myeloid leukemia (AML), 459 patients 15 to 50 years of age were enrolled in the prospective randomized Acute Leukemia French Association-9802 trial. Complete remission was achieved in 89%. A total of 237 patients were then randomized to either TSC consolidation (120 patients) or HDAraC consolidation cycles (117 patients). Overall, there was no significant difference between the 2 consolidation arms (5-year event-free survival [EFS]: 41% for HDAraC vs 35% for TSC), or cumulative incidence of relapse, or treatment-related mortality. Cytogenetically normal AML NPM1+ or CEBPA+ and FLT3-ITD- had the same outcome as those with favorable cytogenetics. When considering favorable and unfavorable risk groups, the trend was in favor of HDAraC. However, the difference became significant when considering intermediate cytogenetics (5-year EFS: 49% vs 29%; P = .02), especially cytogenetically normal AML (5-year EFS: 48% vs 31%; P = .04), which was related to lower relapse rate and less toxicity. This study demonstrates that TSC did not produce any benefit when used as consolidation therapy in younger adults compared with HDAraC. This trial was registered at www.clinicaltrials.gov as #NCT00880243. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00064971
Volume :
118
Issue :
7
Database :
Academic Search Index
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
66873659
Full Text :
https://doi.org/10.1182/blood-2011-04-349258