Risk-Stratified Therapy and the Intensive Use of Cytarabine Improves the Outcome in Childhood Acute Myeloid Leukemia: The AML99 Trial From the Japanese Childhood AML Cooperative Study Group

Author:

Tsukimoto Ichiro1,Tawa Akio1,Horibe Keizo1,Tabuchi Ken1,Kigasawa Hisato1,Tsuchida Masahiro1,Yabe Hiromasa1,Nakayama Hideki1,Kudo Kazuko1,Kobayashi Ryoji1,Hamamoto Kazuko1,Imaizumi Masue1,Morimoto Akira1,Tsuchiya Shigeru1,Hanada Ryoji1

Affiliation:

1. From the Department of Pediatrics, Toho University School of Medicine, Tokyo; Department of Pediatrics, Osaka National Hospital, Osaka; Clinical Research Center, Nagoya Hospital Organization Nagoya Medical Center; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya; Division of Hematology, Kanagawa Children's Medical Center, Yokohama; Department of Pediatrics, Ibaraki Children's Hospital, Mito; Specialized Clinical Science, Pediatrics, Tokai University School of Medicine,...

Abstract

Purpose To improve the prognosis in children with newly diagnosed acute myeloid leukemia (AML) by introducing a dose-dense intensive chemotherapy regimen and an appropriate risk stratification system. Patients and Methods Two hundred forty children with de novo AML were treated with continuous cytarabine-based induction therapy and stratified to three risk groups based on the initial treatment response, age, and WBC at diagnosis and cytogenetics. All of the patients were treated with intensive consolidation chemotherapy including three or four courses of high-dose cytarabine. Allogeneic hematopoietic stem-cell transplantation (HSCT) was indicated for only the intermediate-risk patients with matched related donors and for all the high-risk subsets. Results Two hundred twenty-seven children (94.6%) achieved a complete remission (CR). Four children demonstrated induction death. The median follow-up of the live patients was 55 months (range, 37 to 73 months). The 5-year overall survival of all 240 children was 75.6% (95% CI, 70.3% to 81.4%) and event-free survival was 61.6% (95% CI, 55.8% to 68.1%). The 5-year disease-free survival in each risk group were 71.3% (95% CI, 63.4% to 80.2%) in the low-risk group (n = 112), 59.8% (95% CI, 50.6% to 70.7%) in the intermediate-risk group (n = 92), and 56.5% (95% CI, 39.5% to 80.9%) in the high-risk group (n = 23). Eight children died during the first CR, including four after HSCT. Conclusion A high survival rate, 75.6% at 5 years, was achieved for childhood with de novo AML in the AML99 trial. The treatment strategy was well tolerated with only 1.7% induction death rate and 3.5% remission death rate. Low-risk children were successfully treated with chemotherapy alone.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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