TY - JOUR
T1 - Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors
T2 - A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG)
AU - Hasegawa, Daiichiro
AU - Tawa, Akio
AU - Tomizawa, Daisuke
AU - Watanabe, Tomoyuki
AU - Saito, Akiko Moriya
AU - Kudo, Kazuko
AU - Taga, Takashi
AU - Iwamoto, Shotaro
AU - Shimada, Akira
AU - Terui, Kiminori
AU - Moritake, Hiroshi
AU - Kinoshita, Akitoshi
AU - Takahashi, Hiroyuki
AU - Nakayama, Hideki
AU - Koh, Katsuyoshi
AU - Goto, Hiroaki
AU - Kosaka, Yoshiyuki
AU - Miyachi, Hayato
AU - Horibe, Keizo
AU - Nakahata, Tatsutoshi
AU - Adachi, Souichi
N1 - Funding Information:
This work was supported in part by a Grant‐in‐Aid for Cancer Research from the Ministry of Health, Labour and Welfare of Japan.
Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2020/12/1
Y1 - 2020/12/1
N2 - 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.
AB - 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.
KW - acute myeloid leukemia
KW - childhood
KW - noncore-binding factor
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U2 - 10.1002/pbc.28692
DO - 10.1002/pbc.28692
M3 - Article
C2 - 32886449
AN - SCOPUS:85090135758
SN - 1545-5009
VL - 67
JO - Medical and Pediatric Oncology
JF - Medical and Pediatric Oncology
IS - 12
M1 - e28692
ER -