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A randomized comparison of 4 courses of standard-dose multiagent chemotherapy versus 3 courses of high-dose cytarabine alone in postremission therapy for acute myeloid leukemia in adults: the JALSG AML201 Study.

Authors :
Miyawaki S
Ohtake S
Fujisawa S
Kiyoi H
Shinagawa K
Usui N
Sakura T
Miyamura K
Nakaseko C
Miyazaki Y
Fujieda A
Nagai T
Yamane T
Taniwaki M
Takahashi M
Yagasaki F
Kimura Y
Asou N
Sakamaki H
Handa H
Honda S
Ohnishi K
Naoe T
Ohno R
Source :
Blood [Blood] 2011 Feb 24; Vol. 117 (8), pp. 2366-72. Date of Electronic Publication: 2010 Dec 29.
Publication Year :
2011

Abstract

We conducted a prospective randomized study to assess the optimal postremission therapy for adult acute myeloid leukemia in patients younger than 65 years in the first complete remission. A total of 781 patients in complete remission were randomly assigned to receive consolidation chemotherapy of either 3 courses of high-dose cytarabine (HiDAC, 2 g/m(2) twice daily for 5 days) alone or 4 courses of conventional standard-dose multiagent chemotherapy (CT) established in the previous JALSG AML97 study. Five-year disease-free survival was 43% for the HiDAC group and 39% for the multiagent CT group (P = .724), and 5-year overall survival was 58% and 56%, respectively (P = .954). Among the favorable cytogenetic risk group (n = 218), 5-year disease-free survival was 57% for HiDAC and 39% for multiagent CT (P = .050), and 5-year overall survival was 75% and 66%, respectively (P = .174). In the HiDAC group, the nadir of leukocyte counts was lower, and the duration of leukocyte less than 1.0 × 10(9)/L longer, and the frequency of documented infections higher. The present study demonstrated that the multiagent CT regimen is as effective as our HiDAC regimen for consolidation. Our HiDAC regimen resulted in a beneficial effect on disease-free survival only in the favorable cytogenetic leukemia group. This trial was registered at www.umin.ac.jp/ctr/ as #C000000157.

Details

Language :
English
ISSN :
1528-0020
Volume :
117
Issue :
8
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
21190996
Full Text :
https://doi.org/10.1182/blood-2010-07-295279