TY - JOUR
T1 - Low incidence of osteonecrosis in childhood acute lymphoblastic leukemia treated with ALL-97 and ALL-02 study of Japan association of childhood leukemia study group
AU - Sakamoto, Kenichi
AU - Imamura, Toshihiko
AU - Kihira, Kentaro
AU - Suzuki, Koji
AU - Ishida, Hisashi
AU - Morita, Hiromi
AU - Kanno, Miyako
AU - Mori, Takeshi
AU - Hiramatsu, Hidefumi
AU - Matsubara, Kousaku
AU - Terui, Kiminori
AU - Takahashi, Yoshihiro
AU - Suenobu, So Ichi
AU - Hasegawa, Daiichiro
AU - Kosaka, Yoshiyuki
AU - Kato, Koji
AU - Moriya-Saito, Akiko
AU - Sato, Atsushi
AU - Kawasaki, Hirohide
AU - Yumura-Yagi, Keiko
AU - Hara, Junichi
AU - Hori, Hiroki
AU - Horibe, Keizo
N1 - Publisher Copyright:
© 2018 by American Society of Clinical Oncology.
PY - 2018
Y1 - 2018
N2 - Purpose Osteonecrosis (ON) is a serious complication of the treatment of childhood acute lymphoblastic leukemia (ALL); however, data relating to ON in Asian pediatric patients with ALL are scarce. Therefore, we performed a retrospective analysis of cohorts of Japanese patients with ALL to clarify the incidence, clinical characteristics, and risk factors of ON. Patients and Methods The incidence and characteristics of ON were determined in patients with ALL (n = 1,662) enrolled in two studies from the Japan Association of Childhood Leukemia Study (JACLS) group (n = 635 and n = 1,027 patients treated with the ALL-97 and ALL-02 protocols, respectively). Results In total, 24 of 1,662 patients suffered from ON, of which 12 of 635 and 12 of 1,027 patients were treated with the ALL-97 and the ALL-02 protocol, respectively. Of the 24 patients, 23 were older than 10 years. In multivariate analysis, age ($ 10 years) was the sole significant risk factor for ON (P, .001). Separate evaluation of patients $ 10 years of age indicated a 5-year cumulative incidence of ON of 7.2% (95% CI, 4.0% to 12.6%) and 5.9% (95% CI, 3.3% to 10.4%) in the ALL-97 and the ALL-02 protocol, respectively, which was lower than reported previously, despite an administration of dexamethasone (DEX) similar to that in comparable studies; however, concomitant administration of DEX and L-asparaginase was reduced in the JACLS protocols. Conclusion We identified a low frequency of ON in the JACLS ALL-97 and ALL-02 studies. Although the sole risk factor for ON was age ($ 10 years), even among high-risk patients, ON incidence was significantly lower than that reported in previous studies. These results suggest that, not only the total amount of DEX, but also how DEX and L-asparaginase are administered, which affects the clearance of DEX, may be associated with ON incidence in patients with ALL.
AB - Purpose Osteonecrosis (ON) is a serious complication of the treatment of childhood acute lymphoblastic leukemia (ALL); however, data relating to ON in Asian pediatric patients with ALL are scarce. Therefore, we performed a retrospective analysis of cohorts of Japanese patients with ALL to clarify the incidence, clinical characteristics, and risk factors of ON. Patients and Methods The incidence and characteristics of ON were determined in patients with ALL (n = 1,662) enrolled in two studies from the Japan Association of Childhood Leukemia Study (JACLS) group (n = 635 and n = 1,027 patients treated with the ALL-97 and ALL-02 protocols, respectively). Results In total, 24 of 1,662 patients suffered from ON, of which 12 of 635 and 12 of 1,027 patients were treated with the ALL-97 and the ALL-02 protocol, respectively. Of the 24 patients, 23 were older than 10 years. In multivariate analysis, age ($ 10 years) was the sole significant risk factor for ON (P, .001). Separate evaluation of patients $ 10 years of age indicated a 5-year cumulative incidence of ON of 7.2% (95% CI, 4.0% to 12.6%) and 5.9% (95% CI, 3.3% to 10.4%) in the ALL-97 and the ALL-02 protocol, respectively, which was lower than reported previously, despite an administration of dexamethasone (DEX) similar to that in comparable studies; however, concomitant administration of DEX and L-asparaginase was reduced in the JACLS protocols. Conclusion We identified a low frequency of ON in the JACLS ALL-97 and ALL-02 studies. Although the sole risk factor for ON was age ($ 10 years), even among high-risk patients, ON incidence was significantly lower than that reported in previous studies. These results suggest that, not only the total amount of DEX, but also how DEX and L-asparaginase are administered, which affects the clearance of DEX, may be associated with ON incidence in patients with ALL.
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U2 - 10.1200/JCO.2017.75.5066
DO - 10.1200/JCO.2017.75.5066
M3 - Article
C2 - 29360413
AN - SCOPUS:85044188260
SN - 0732-183X
VL - 36
SP - 900
EP - 907
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 9
ER -