Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG)

  • Daiichiro Hasegawa
  • , Akio Tawa
  • , Daisuke Tomizawa
  • , Tomoyuki Watanabe
  • , Akiko Moriya Saito
  • , Kazuko Kudo
  • , Takashi Taga
  • , Shotaro Iwamoto
  • , Akira Shimada
  • , Kiminori Terui
  • , Hiroshi Moritake
  • , Akitoshi Kinoshita
  • , Hiroyuki Takahashi
  • , Hideki Nakayama
  • , Katsuyoshi Koh
  • , Hiroaki Goto
  • , Yoshiyuki Kosaka
  • , Hayato Miyachi
  • , Keizo Horibe
  • , Tatsutoshi Nakahata
  • Souichi Adachi

Research output: Contribution to journalArticlepeer-review

Abstract

We previously reported that risk-stratified therapy and intensive postremission chemotherapy (PRC) contributed to the improved survival of childhood acute myeloid leukemia (AML) in the AML99 study, which led us to consider a reduction in the number of PRC courses with more restrictive indications for stem cell transplantation (SCT) in the successor AML-05 study. We here report the outcome of AML patients without core-binding factor mutation (non-CBF AML) in the AML-05 study. Two-hundred eighty-nine children (age < 18 years old) with non-CBF AML were eligible. Patients with unfavorable cytogenetics and/or poor bone marrow response to the first induction course were candidates for SCT in the AML-05 study. After two courses of induction, a further three courses of PRC were given in AML-05, while four courses were given in the AML99 study. The 3-year event-free survival (EFS) rate in the AML-05 study (46.7%, 95% CI: 40.6-52.6%) was comparable to that of non-CBF AML in the AML99 study (51.5%, 95% CI: 42.7-59.6%) (P =.16). However, the 3-year overall survival (OS) rate in the AML-05 study (62.9%, 95% CI: 56.3-68.8%) was slightly lower than that in the AML99 study (71.6%, 95% CI: 63.2-78.5%) (P =.060), mainly due to decreased remission induction rate and increased nonrelapsed mortality. In conclusion, reductions in the number of PRC courses from four to three, together with repetitive cycles of high-dose cytarabine, were acceptable for non-CBF childhood AML.

Original languageEnglish
Article numbere28692
JournalPediatric Blood and Cancer
Volume67
Issue number12
DOIs
Publication statusPublished - 01-12-2020
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Hematology
  • Oncology

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