TY - JOUR
T1 - Neurocognitive functioning of children treated for high-risk B-acute lymphoblastic leukemia randomly assigned to different methotrexate and corticosteroid treatment strategies
T2 - A report from the children's oncology group
AU - Hardy, Kristina K.
AU - Embry, Leanne
AU - Kairalla, John A.
AU - Helian, Shanjun
AU - Devidas, Meenakshi
AU - Armstrong, Daniel
AU - Hunger, Stephen
AU - Carroll, William L.
AU - Larsen, Eric
AU - Raetz, Elizabeth A.
AU - Loh, Mignon L.
AU - Yang, Wenjian
AU - Relling, Mary V.
AU - Noll, Robert B.
AU - Winick, Naomi
N1 - Publisher Copyright:
Copyright © 2017 American Society of Clinical Oncology. All rights reserved.
PY - 2017/8/10
Y1 - 2017/8/10
N2 - Purpose Survivors of childhood acute lymphoblastic leukemia (ALL) are at risk for neurocognitive deficits that are associated with treatment, individual, and environmental factors. This study examined the impact of different methotrexate (MTX) and corticosteroid treatment strategies on neurocognitive functioning in children with high-risk B-lineage ALL. Methods Participants were randomly assigned to receive high-dose MTX with leucovorin rescue or escalating dose MTX with PEG asparaginase without leucovorin rescue. Patients were also randomly assigned to corticosteroid therapy that included either dexamethasone or prednisone. A neurocognitive evaluation of intellectual functioning (IQ), working memory, and processing speed (PS) was conducted 8 to 24 months after treatment completion (n = 192). Results The method of MTX delivery and corticosteroid assignment were unrelated to differences in neurocognitive outcomes after controlling for ethnicity, race, age, gender, insurance status, and time off treatment; however, survivors who were age <10 years at diagnosis (n = 89) had significantly lower estimated IQ (P < .001) and PS scores (P = .02) compared with participants age ≥ 10 years. In addition, participants who were covered by US public health insurance had estimated IQs that were significantly lower (P <.001) than those with US private or military insurance. Conclusion Children with high-risk B-lineage ALL who were age <10 years at diagnosis are at risk for deficits in IQ and PS in the absence of cranial radiation, regardless of MTX delivery or corticosteroid type. These data may serve as a basis for developing screening protocols to identify children who are at high risk for deficits so that early intervention can be initiated to mitigate the impact of therapy on neurocognitive outcomes.
AB - Purpose Survivors of childhood acute lymphoblastic leukemia (ALL) are at risk for neurocognitive deficits that are associated with treatment, individual, and environmental factors. This study examined the impact of different methotrexate (MTX) and corticosteroid treatment strategies on neurocognitive functioning in children with high-risk B-lineage ALL. Methods Participants were randomly assigned to receive high-dose MTX with leucovorin rescue or escalating dose MTX with PEG asparaginase without leucovorin rescue. Patients were also randomly assigned to corticosteroid therapy that included either dexamethasone or prednisone. A neurocognitive evaluation of intellectual functioning (IQ), working memory, and processing speed (PS) was conducted 8 to 24 months after treatment completion (n = 192). Results The method of MTX delivery and corticosteroid assignment were unrelated to differences in neurocognitive outcomes after controlling for ethnicity, race, age, gender, insurance status, and time off treatment; however, survivors who were age <10 years at diagnosis (n = 89) had significantly lower estimated IQ (P < .001) and PS scores (P = .02) compared with participants age ≥ 10 years. In addition, participants who were covered by US public health insurance had estimated IQs that were significantly lower (P <.001) than those with US private or military insurance. Conclusion Children with high-risk B-lineage ALL who were age <10 years at diagnosis are at risk for deficits in IQ and PS in the absence of cranial radiation, regardless of MTX delivery or corticosteroid type. These data may serve as a basis for developing screening protocols to identify children who are at high risk for deficits so that early intervention can be initiated to mitigate the impact of therapy on neurocognitive outcomes.
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U2 - 10.1200/JCO.2016.71.7587
DO - 10.1200/JCO.2016.71.7587
M3 - Article
C2 - 28671857
AN - SCOPUS:85028762924
SN - 0732-183X
VL - 35
SP - 2700
EP - 2707
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 23
ER -