首页 | 本学科首页   官方微博 | 高级检索  
检索        


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 Shuichi  Ohtake Shigeki  Fujisawa Shin  Kiyoi Hitoshi  Shinagawa Katsuji  Usui Noriko  Sakura Toru  Miyamura Koichi  Nakaseko Chiaki  Miyazaki Yasushi  Fujieda Atsushi  Nagai Tadashi  Yamane Takahisa  Taniwaki Masafumi  Takahashi Masatomo  Yagasaki Fumiharu  Kimura Yukihiko  Asou Norio  Sakamaki Hisashi  Handa Hiroshi  Honda Sumihisa  Ohnishi Kazunori  Naoe Tomoki  Ohno Ryuzo
Institution:Leukemia Research Center, Saiseikai Maebashi Hospital, Maebashi, Japan. miyawaki@mail.wind.ne.jp
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.
Keywords:
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号