FLAG-IDA as frontline induction improves outcomes in pediatric patients with core-binding factor or KMT2A-rearranged acute myeloid leukemia: A multicenter cohort study in southern China

Y Yongzhi Zheng (2Fujian Medical University Union Hospital, Fuzhou, China) J Jian Li H Huiping Li M Mincui Zheng (4Hunan Children's Hospital, Changsha, China) B Benshan Zhang (4Hunan Children's Hospital, Changsha, China) H Huirong Mai (5Shenzhen Children's Hospital, Shenzhen, China) S Sixi Liu (5Shenzhen Children's Hospital, Shenzhen, China) C Changgang Li L Lihua Yang L L Yu (6Zhujiang Hospital of Southern Medical University, Guangzhou, China) H Hua Jiang Y Yingyi He (7Guangzhou Women and Children's Medical Center, Guangzhou, China) X Xiangling He K Keke Chen H Hong Wen H Honggui Xu (10Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China) N Nainong Li (1Fujian Institute of Hematology, Fujian Provincial Key Laboratory on Hematology, Fujian Medical University Union Hospital, fuzhou, China) Z Zhiyong Peng (State Key Laboratory of Radiation Medicine and Protection, School for Radiological and Interdisciplinary Sciences (RAD-X) and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions) C Chunfu Li (1Nanfang-Chunfu Children's Institute of Hematology & Oncology, Dongguan TaiXin Hospital, Dongguan City, China) X Xiaoqin Feng

Abstract

Abstract Background: The FLAG-IDA (fludarabine, high-dose cytarabine, granulocyte colony-stimulating factor, and idarubicin) regimen is rarely used as frontline induction therapy for pediatric patients with de novo acute myeloid leukemia (AML). Therefore, this study aimed to assess the efficacy and safety of FLAG-IDA for frontline induction in pediatric patients with de novo AML and to analyze the treatment responses across various molecular subgroups. Methods: In this multicenter retrospective study, we evaluated the efficacy of FLAG-IDA (n=681; Group A) versus DAE (daunorubicin, Ara-C, and etoposide; n=194; Group B) induction as induction therapy, followed by two courses of consolidation therapy in 875 pediatric patients with de novo AML (2015–2023) in southern China. High-risk patients were advised to undergo hematopoietic stem cell transplantation (HSCT). Outcomes assessed included complete remission (CR), overall survival (OS), event-free survival, and treatment-related mortality. Results: In total, 875 patients were included in this study [median age at diagnosis: 6.4 years (range, 0.5–14.0 years)]. Although cumulative CR and treatment-related mortality rates after two induction cycles did not differ significantly between Group A and Group B (CR rate: 92.4%vs. 88.9%, p=0.134; treatment-related mortality rate: 4.3% vs. 6.0%, p=0.324); Group A demonstrated a better 5-year OS (79.6% vs. 69.3%, p=0.006). Among patients with core-binding factor AML (CBF-AML), FLAG-IDA induction significantly improved OS compared with DAE (5-year OS: 90.4% vs. 78.4%; p=0.031). Similarly, superior outcomes were observed in KMT2A-rearranged AML (80.8% vs. 61.3%; p=0.044). FLT3-ITD patients derived significant benefit from HSCT in first CR. However, non-MLLT3 KMT2A-rearranged patients who achieved first CR demonstrated comparable outcomes whether consolidated with chemotherapy alone or HSCT. Conclusions: These findings indicate that frontline induction with FLAG-IDA, followed by two courses of consolidation, shortens chemotherapy duration, confers a significant survival advantage in pediatric CBF-AML, and achieves long-term outcomes, comparable with those achieved with HSCT in non-MLLT3 KMT2A-rearranged AML.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 5152-5152
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (20)

Y

Yongzhi Zheng

2Fujian Medical University Union Hospital, Fuzhou, China

J

Jian Li

H

Huiping Li

M

Mincui Zheng

4Hunan Children's Hospital, Changsha, China

B

Benshan Zhang

4Hunan Children's Hospital, Changsha, China

H

Huirong Mai

5Shenzhen Children's Hospital, Shenzhen, China

S

Sixi Liu

5Shenzhen Children's Hospital, Shenzhen, China

C

Changgang Li

L

Lihua Yang

L

L Yu

6Zhujiang Hospital of Southern Medical University, Guangzhou, China

H

Hua Jiang

Y

Yingyi He

7Guangzhou Women and Children's Medical Center, Guangzhou, China

X

Xiangling He

K

Keke Chen

H

Hong Wen

H

Honggui Xu

10Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China

N

Nainong Li

1Fujian Institute of Hematology, Fujian Provincial Key Laboratory on Hematology, Fujian Medical University Union Hospital, fuzhou, China

Z

Zhiyong Peng

State Key Laboratory of Radiation Medicine and Protection, School for Radiological and Interdisciplinary Sciences (RAD-X) and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions

C

Chunfu Li

1Nanfang-Chunfu Children's Institute of Hematology & Oncology, Dongguan TaiXin Hospital, Dongguan City, China

X

Xiaoqin Feng