医学
微小残留病
内科学
完全缓解
肿瘤科
胃肠病学
化疗
白血病
作者
Weina Zhang,Jiaoyang Cai,Xiang Wang,Yani Ma,Xiaofan Zhu,Jie Yu,Peifang Xiao,Ju Gao,Yongjun Fang,Changda Liang,Xue Li,Fen Zhou,Xiaowen Zhai,Xiaoxiao Xu,Xin Tian,Aiguo Liu,Ningling Wang,Jia‐Shi Zhu,Lingzhen Wang,Frankie Wai Tsoi Cheng
出处
期刊:Blood
[American Society of Hematology]
日期:2024-12-30
卷期号:145 (17): 1890-1902
被引量:2
标识
DOI:10.1182/blood.2024026381
摘要
Abstract We evaluated the prognostic and therapeutic significance of measurable residual disease (MRD) during remission induction in pediatric patients with acute lymphoblastic leukemia (ALL). In the Chinese Children Cancer Group ALL 2015 protocol, 7640 patients were categorized into low-, intermediate-, or high-risk groups based on clinical and genetic features. Final risk classification was determined by assessing MRD using flow cytometry on days 19 and 46 of remission induction with additional intensified chemotherapy for day 19 MRD ≥1%. Patients with B-ALL with negative MRD (<0.01%) on day 19 or day 46 had significantly better 5-year event-free survival (EFS) than those with MRD of between 0.01% and 0.99% who, in turn, had better EFS than patients with MRD of ≥1%. Provisional low-risk patients with day 19 MRD ≥1% but negative day 46 MRD who were reclassified as intermediate risk had a 5-year EFS that was comparable with that of low-risk patients with day 19 MRD of 0.3% to 0.99% and negative day 46 MRD (82.5% vs 83.0%) and better EFS than provisional low-risk patients with MRD on both days (83.0% vs 72.6%; P < .001). Similarly, patients with provisional intermediate-risk B-ALL with day 19 MRD ≥1% but negative day 46 MRD who received additional therapy had better 5-year EFS than those with day 19 MRD between 0.3% and 0.99% (70.7% vs 53.0%; P < .001). Among low-risk patients with negative day 46 MRD, those with negative day 19 MRD had superior EFS than those with positive day 19 MRD (91.7% vs 86.1%; P < .001). Optimal use of day 19 MRD could improve individualized treatment and outcomes. This trial was registered at www.chictr.org.cn as #ChiCTR-IPR-14005706.
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