TY - JOUR
T1 - Appropriate dose reduction in induction therapy is essential for the treatment of infants with acute myeloid leukemia
T2 - A report from the japanese pediatric leukemia/lymphoma study group
AU - Tomizawa, Daisuke
AU - Tawa, Akio
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 - Kiyokawa, Nobutaka
AU - Isoyama, Keiichi
AU - Mizutani, Shuki
AU - Hara, Junichi
AU - Horibe, Keizo
AU - Nakahata, Tatsutoshi
AU - Adachi, Souichi
N1 - Funding Information:
Acknowledgments This work was supported by a Grant for Clinical Cancer Research and a Grant-in-Aid for Cancer Research from the Ministry of Health, Labour, and Welfare of Japan.
PY - 2013/11
Y1 - 2013/11
N2 - Infants (<1 year old) with acute myeloid leukemia (AML) are particularly vulnerable to intensive cytotoxic therapy. Indeed, the mortality rate was high among infants enrolled in the Japanese Pediatric Leukemia/ Lymphoma Study Group AML-05 study, which prompted us to temporarily suspend patient enrollment and amend the protocol. Forty-five infants with AML were enrolled. For patients aged < 2 years, drug doses were adjusted for body weight. Following the protocol amendments, doses for infants were reduced by a further 33 % in the initial induction course. Six infants died during the induction phase (including five early deaths), mainly due to pulmonary complications. The 3-year probability of overall survival (pOS) in all 45 infants [55.9 %, 95 % confidence interval (CI) 37.9-70.6 %] was significantly lower than that of patients aged 1 to <2 years (77.0 %, 95 % CI 62.7-86.3 %) and those aged ≥ 2 years (74.7 %, 95 % CI 69.2-79.4 %) (P = 0.037), mainly due to the higher nonrelapse mortality rate in infants. No early deaths occurred after the protocol amendments, and the 3-year pOS of the 17 infants enrolled thereafter was 76.4 % (95 % CI 48.8-90.4 %). In conclusion, appropriate dose reduction is essential to avoid early deaths when treating infants with AML.
AB - Infants (<1 year old) with acute myeloid leukemia (AML) are particularly vulnerable to intensive cytotoxic therapy. Indeed, the mortality rate was high among infants enrolled in the Japanese Pediatric Leukemia/ Lymphoma Study Group AML-05 study, which prompted us to temporarily suspend patient enrollment and amend the protocol. Forty-five infants with AML were enrolled. For patients aged < 2 years, drug doses were adjusted for body weight. Following the protocol amendments, doses for infants were reduced by a further 33 % in the initial induction course. Six infants died during the induction phase (including five early deaths), mainly due to pulmonary complications. The 3-year probability of overall survival (pOS) in all 45 infants [55.9 %, 95 % confidence interval (CI) 37.9-70.6 %] was significantly lower than that of patients aged 1 to <2 years (77.0 %, 95 % CI 62.7-86.3 %) and those aged ≥ 2 years (74.7 %, 95 % CI 69.2-79.4 %) (P = 0.037), mainly due to the higher nonrelapse mortality rate in infants. No early deaths occurred after the protocol amendments, and the 3-year pOS of the 17 infants enrolled thereafter was 76.4 % (95 % CI 48.8-90.4 %). In conclusion, appropriate dose reduction is essential to avoid early deaths when treating infants with AML.
KW - Acute myeloid leukemia
KW - Acute respiratory distress syndrome
KW - Early death
KW - Infants
UR - http://www.scopus.com/inward/record.url?scp=84892916628&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84892916628&partnerID=8YFLogxK
U2 - 10.1007/s12185-013-1429-2
DO - 10.1007/s12185-013-1429-2
M3 - Article
C2 - 24068655
AN - SCOPUS:84892916628
SN - 0925-5710
VL - 98
SP - 578
EP - 588
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 5
ER -