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Reduced Dose Intensity of Daunorubicin During Remission Induction for Low-Risk Patients With Acute Lymphoblastic Leukemia: A Retrospective Cohort Study of the Chinese Children's Cancer Group. | LitMetric

AI Article Synopsis

  • The study aimed to find a way to reduce the negative effects of chemotherapy in children with low-risk acute lymphoblastic leukemia (ALL) while still achieving high cure rates.
  • Researchers analyzed data from 2396 patients in the CCCG-ALL-2015 study, comparing outcomes between those receiving a single dose and those receiving a double dose of daunorubicin during the remission-induction phase.
  • Results showed no significant differences in overall survival or early death rates between the groups, but the double-dose group had better event-free survival and lower relapse risk, indicating the possibility of dosage reduction for specific low-risk patients with positive or hyperdiploid ALL.

Article Abstract

Unlabelled: It is urgently necessary to reduce the adverse effects of chemotherapy while maintaining their cure high rates for children with acute lymphoblastic leukemia (ALL). The present study aimed to determine whether the dose intensity of daunorubicin during the remission-induction phase could be reduced for low-risk patients with ALL. A total of 2396 eligible patients, who participated in CCCG-ALL-2015 study and were provisionally assigned to the low-risk group, were included and divided into single-dose group and double-dose group according to the dosage of daunorubicin during the remission-induction phase. For patients with positive ALL or hyperdiploidy ALL, there were no significant differences in outcomes between the two groups. For other patients, the 5-year event-free survival rate was significantly better and the 5-year cumulative risk of any relapse was significantly lower in the double-dose group compared with the single-dose group. Both the 5-year overall survival rate and the risk of early deaths were not significantly different between the two groups. Our results suggested that only B-lineage ALL patients with positivity or hyperdiploidy who achieved an early negative minimal residual disease status were suitable candidates for dosage reduction of daunorubicin during the remission-induction phase.

Clinical Trial Registration: http://www.chictr.org.cn/showproj.aspx?proj=10115, identifier ChiCTR-IPR-14005706.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209708PMC
http://dx.doi.org/10.3389/fonc.2022.911567DOI Listing

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