TY - JOUR
T1 - Comparison of high-dose cytarabine and timed-sequential chemotherapy as consolidation for younger adults with AML in first remission
T2 - The alfa-9802 study
AU - Thomas, Xavier
AU - Elhamri, Mohamed
AU - Raffoux, Emmanuel
AU - Renneville, Aline
AU - Pautas, Cécile
AU - De Botton, Stéphane
AU - De Revel, Thierry
AU - Reman, Oumedaly
AU - Terré, Christine
AU - Gardin, Claude
AU - Chelghoum, Youcef
AU - Boissel, Nicolas
AU - Quesnel, Bruno
AU - Hicheri, Yosr
AU - Bourhis, Jean Henri
AU - Fenaux, Pierre
AU - Preudhomme, Claude
AU - Michallet, Mauricette
AU - Castaigne, Sylvie
AU - Dombret, Hervé
PY - 2011/8/18
Y1 - 2011/8/18
N2 - 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 LeukemiaFrench 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 normalAML (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.
AB - 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 LeukemiaFrench 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 normalAML (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.
UR - http://www.scopus.com/inward/record.url?scp=80051877778&partnerID=8YFLogxK
U2 - 10.1182/blood-2011-04-349258
DO - 10.1182/blood-2011-04-349258
M3 - Article
C2 - 21690555
AN - SCOPUS:80051877778
SN - 0006-4971
VL - 118
SP - 1754
EP - 1762
JO - Blood
JF - Blood
IS - 7
ER -