TY - JOUR
T1 - Treatment of relapsed acute lymphoblastic leukemia in children
T2 - an observational study of the Japan Children’s Cancer Group
AU - Goto, Hiroaki
AU - Kada, Akiko
AU - Ogawa, Chitose
AU - Nishiuchi, Ritsuo
AU - Yamanaka, Junko
AU - Iguchi, Akihiro
AU - Nishi, Masanori
AU - Sakaguchi, Kimiyoshi
AU - Kumamoto, Tadashi
AU - Mochizuki, Shinji
AU - Ueki, Hideaki
AU - Kosaka, Yoshiyuki
AU - Saito, Akiko M.
AU - Toyoda, Hidemi
N1 - Publisher Copyright:
© Japanese Society of Hematology 2024.
PY - 2024/11
Y1 - 2024/11
N2 - The Japan Children’s Cancer Group Relapsed Acute Lymphoblastic Leukemia (ALL) Committee conducted a prospective observational study (ALL-R14) to explore promising reinduction therapy regimens for relapsed ALL to investigate in future trials. In Japan, clofarabine- and bortezomib-based regimens were of interest since they were newly introduced for ALL in the study period (2015–2018). Seventy-five pediatric patients were enrolled in total. The 2-year event-free/overall survival rates in patients with first (n = 59) or second (n = 11) relapse were 40.1% (95% confidence interval [CI]: 25.5–52.3%)/66.3% (95% CI 52.3–77.0%) and 34.1% (95% CI 9.1–61.6%)/62.3% (95% CI 27.7–84.0%), respectively. Clofarabine- or bortezomib-based regimens were used only in patients with high-risk disease. The first reinduction therapy used in the 41 patients with early or multiple relapsed B-cell precursor ALL was clofarabine in 7 patients and bortezomib in 9 patients. The odds ratio for reinduction failure risk with a clofarabine- or bortezomib-based regimen compared with other regimens was 9.0 (95% CI 0.9–86.4, P = 0.057) or 1.9 (95% CI 0.4–8.7, P = 0.42), respectively. Thus, clofarabine- or bortezomib-based regimens had no obvious advantage as reinduction therapy for relapsed ALL in children.
AB - The Japan Children’s Cancer Group Relapsed Acute Lymphoblastic Leukemia (ALL) Committee conducted a prospective observational study (ALL-R14) to explore promising reinduction therapy regimens for relapsed ALL to investigate in future trials. In Japan, clofarabine- and bortezomib-based regimens were of interest since they were newly introduced for ALL in the study period (2015–2018). Seventy-five pediatric patients were enrolled in total. The 2-year event-free/overall survival rates in patients with first (n = 59) or second (n = 11) relapse were 40.1% (95% confidence interval [CI]: 25.5–52.3%)/66.3% (95% CI 52.3–77.0%) and 34.1% (95% CI 9.1–61.6%)/62.3% (95% CI 27.7–84.0%), respectively. Clofarabine- or bortezomib-based regimens were used only in patients with high-risk disease. The first reinduction therapy used in the 41 patients with early or multiple relapsed B-cell precursor ALL was clofarabine in 7 patients and bortezomib in 9 patients. The odds ratio for reinduction failure risk with a clofarabine- or bortezomib-based regimen compared with other regimens was 9.0 (95% CI 0.9–86.4, P = 0.057) or 1.9 (95% CI 0.4–8.7, P = 0.42), respectively. Thus, clofarabine- or bortezomib-based regimens had no obvious advantage as reinduction therapy for relapsed ALL in children.
KW - Acute lymphoblastic leukemia
KW - Bortezomib
KW - Children
KW - Clofarabine
KW - Relapse
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U2 - 10.1007/s12185-024-03838-5
DO - 10.1007/s12185-024-03838-5
M3 - Article
C2 - 39190256
AN - SCOPUS:85202195221
SN - 0925-5710
VL - 120
SP - 631
EP - 638
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 5
ER -