4.6 Article

Outcome of children with newly diagnosed acute lymphoblastic leukemia treated with CCLG-ALL 2008: The first nation-wide prospective multicenter study in China

期刊

AMERICAN JOURNAL OF HEMATOLOGY
卷 93, 期 7, 页码 913-920

出版社

WILEY
DOI: 10.1002/ajh.25124

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资金

  1. National Key Technology R&D Program of China [2007BAI04B03]
  2. National Science and Technology Major Project of the Ministry of Science and Technology of China [2017ZX09304029]
  3. National Natural Science Foundation of China [81200392, 81170504]
  4. Beijing Natural Science Foundation [7152054]
  5. Scientific Research Common Program of Beijing Municipal Commission of Education [KM201810025025]
  6. Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Grant [ZY201404]
  7. Beijing Municipal Administration of Hospitals DengFeng Program [DFL20151101]
  8. Capital Health and Development of Special Grant [2016-12091]
  9. Tianjin Science and Technology Program [12ZCDZSY18100]
  10. Children Cancer Foundation of Hong Kong
  11. New Sunshine Charity Foundation of China

向作者/读者索取更多资源

Acute lymphoblastic leukemia (ALL) is the most common malignancy among children. The trial Chinese Children Leukemia Group (CCLG)-ALL 2008 was a prospective clinical trial designed to improve treatment outcome of childhood ALL through the first nation-wide collaborative study in China. Totally 2231 patients were recruited from ten tertiary hospitals in eight cities. The patients were stratified according to clinical-biological characteristics and early treatment response. Standard risk (SR) and intermediate risk (IR) groups were treated with a modified BFM based protocol, and there was 25%-50% dose reduction during intensification phases in the SR group. Patients in high risk (HR) group received a more intensive maintenance treatment. Minimal residual disease (MRD) monitoring with treatment adjustment was performed in two hospitals (the MRD group). Complete remission (CR) was achieved in 2100 patients (94.1%). At five years, the estimate for overall survival (OS) and event-free survival (EFS) of the whole group was 85.3% and 79.9%, respectively. The cumulative incidence of relapse (CIR) was 15.3% at five years. The OS, EFS and CIR for the SR group were 91.5%, 87.9%, and 9.7%, respectively. The outcome of the MRD group is better than the non-MRD group (5y-EFS: 82.4% vs 78.3%, P=.038; 5y-CIR: 10.7% vs 18.0%, P<.001). Our results demonstrated that the large-scale multicenter trial for pediatric ALL was feasible in China. Dose reduction in the SR group could achieve high EFS. MRD-based risk stratification might improve the treatment outcome for childhood ALL.

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