| Literature DB >> 29675840 |
Lei Cui1,2, Zhi-Gang Li1,2, Yi-Huan Chai3, Jie Yu4, Ju Gao5, Xiao-Fan Zhu6, Run-Ming Jin7, Xiao-Dong Shi8, Le-Ping Zhang9, Yi-Jin Gao10, Rui-Dong Zhang1, Hu-Yong Zheng1, Shao-Yan Hu3, Ying-Hui Cui4, Yi-Ping Zhu5, Yao Zou6, Margaret H L Ng11, Yan Xiao7, Jun-Hui Li8, Yong-Hong Zhang1, Hai-Long He3, Ying Xian4, Tian-You Wang1, Chi-Kong Li12, Min-Yuan Wu1.
Abstract
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.Entities:
Mesh:
Year: 2018 PMID: 29675840 DOI: 10.1002/ajh.25124
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047