Erschienen in:
01.03.2010 | Original Article
Randomized trial of response-oriented individualized versus fixed-schedule induction chemotherapy with idarubicin and cytarabine in adult acute myeloid leukemia: the JALSG AML95 study
verfasst von:
Shigeki Ohtake, Shuichi Miyawaki, Hitoshi Kiyoi, Yasushi Miyazaki, Hirokazu Okumura, Shin Matsuda, Tadashi Nagai, Yuji Kishimoto, Masaya Okada, Masatomo Takahashi, Hiroshi Handa, Jin Takeuchi, Shinichi Kageyama, Norio Asou, Fumiharu Yagasaki, Yasuhiro Maeda, Kazunori Ohnishi, Tomoki Naoe, Ryuzo Ohno
Erschienen in:
International Journal of Hematology
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Ausgabe 2/2010
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Abstract
A multicenter, prospective, randomized study was conducted to compare a response-oriented individualized remission induction therapy with a standard fixed-schedule induction therapy, using idarubicin (IDR) and cytarabine (Ara-C), in adult patients with acute myeloid leukemia (AML). Newly diagnosed patients with AML of age less than 65 were randomly assigned to receive either of the two schedules. Both groups received IDR (12 mg/m2) for 3 days and Ara-C (100 mg/m2) for 7 days. In the individualized group, if the bone marrow on day 8 did not become hypocellular with less than 15% blasts, patients received additional IDR for one more day and Ara-C for 2 or 3 more days. Patients achieving complete remission (CR) received the same post-remission therapy. The CR rate was 79.4% for the individualized group (n = 209) and 81.9% for the fixed group (n = 221) (p = 0.598). At a median follow-up of 81 months, 7-year predicted overall survival was 37% for the individualized group and 39% for the fixed group (p = 0.496), and 7-year predicted event-free survival was 22% for the individualized group and 23% for the fixed group (p = 0.546). Thus, the present study could not demonstrate any advantage of a response-oriented individualized induction therapy over a fixed-schedule induction therapy in this protocol setting.