Prospective Randomized Comparison of Idarubicin and High-Dose Daunorubicin in Induction Chemotherapy for Newly Diagnosed Acute Myeloid Leukemia

Author:

Lee Je-Hwan1,Kim Hawk1,Joo Young-Don1,Lee Won-Sik1,Bae Sung Hwa1,Zang Dae Young1,Kwon Jihyun1,Kim Min Kyoung1,Lee Junglim1,Lee Gyeong Won1,Lee Jung-Hee1,Choi Yunsuk1,Kim Dae-Young1,Hur Eun-Hye1,Lim Sung-Nam1,Lee Sang-Min1,Ryoo Hun Mo1,Kim Hyo Jung1,Hyun Myung Soo1,Lee Kyoo-Hyung1,

Affiliation:

1. Je-Hwan Lee, Jung-Hee Lee, Dae-Young Kim, Eun-Hye Hur, and Kyoo-Hyung Lee, Asan Medical Center, University of Ulsan College of Medicine, Seoul; Hawk Kim and Yunsuk Choi, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan; Young-Don Joo and Sung-Nam Lim, Haeundae Paik Hospital, Inje University College of Medicine; Won-Sik Lee and Sang-Min Lee, Busan Paik Hospital, Inje University College of Medicine, Busan; Sung Hwa Bae and Hun Mo Ryoo, Daegu Catholic University Medical Center,...

Abstract

Purpose We compared two induction regimens, idarubicin (12 mg/m2/d for 3 days) versus high-dose daunorubicin (90 mg/m2/d for 3 days), in young adults with newly diagnosed acute myeloid leukemia (AML). Patients and Methods A total of 299 patients (149 randomly assigned to cytarabine plus idarubicin [AI] and 150 assigned to cytarabine plus high-dose daunorubicin [AD]) were analyzed. All patients received cytarabine (200 mg/m2/d for 7 days). Results Complete remission (CR) was induced in 232 patients (77.6%), with no difference in CR rates between the AI and AD arms (80.5% v 74.7%, respectively; P = .224). At a median follow-up time of 34.9 months, survival and relapse rates did not differ between the AI and AD arms (4-year overall survival, 51.1% v 54.7%, respectively; P = .756; cumulative incidence of relapse, 35.2% v 25.1%, respectively; P = .194; event-free survival, 45.5% v 50.8%, respectively; P = .772). Toxicity profiles were also similar in the two arms. Interestingly, overall and event-free survival times of patients with FLT3 internal tandem duplication (ITD) mutation were significantly different (AI v AD: median overall survival, 15.5 months v not reached, respectively; P = .030; event-free survival, 11.9 months v not reached, respectively; P = .028). Conclusion This phase III trial comparing idarubicin with high-dose daunorubicin did not find significant differences in CR rates, relapse, and survival. Significant interaction between the treatment arm and the FLT3-ITD mutation was found, and high-dose daunorubicin was more effective than idarubicin in patients with FLT3-ITD mutation.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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