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基于微小残留病和方案驱动的早期反应风险分类强化治疗可提高儿童急性淋巴细胞白血病的生存率。

Improved survival in pediatric acute lymphoblastic leukemia through therapy intensification based on minimal residual disease and protocol-driven early response risk classification.

作者信息

Kim Hyery, Yoon Su Hyun, Kang Sunghan, Koh Kyung-Nam, Im Ho Joon, Chu Daehyun, Kim Mi Young, Cho Young-Uk, Hwang Sang-Hyun, Jang Seongsoo

机构信息

Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.

Department of Laboratory Medicine, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.

出版信息

Blood Res. 2025 Jul 9;60(1):40. doi: 10.1007/s44313-025-00085-3.

Abstract

PURPOSE

Minimal residual disease (MRD)-guided therapy is the global standard treatment for pediatric acute lymphoblastic leukemia (ALL). We assessed the impact of MRD-driven intensification along with protocol-defined risk groups in pediatric ALL treatment.

METHODS

This retrospective analysis included 209 patients with ALL (treated between January 2013 to June 2023). MRD was assessed using six- to eight-color flow cytometry at the end of each phase before the maintenance phase. Post-induction treatment was determined based on early response, National Cancer Institute risk, and cytogenetics. High-risk (HR) patients followed the Korean HR or CCG-1882 protocols and standard-risk (SR) patients followed the modified COG-AALL0331 protocol. Treatment was intensified if flow-MRD ≥ 0.1% was identified.

RESULTS

Overall, 103 and 106 patients were classified as having SR and HR, respectively. The 5-year overall survival (OS) and event-free survival (EFS) were 92.5% and 84.3%, respectively. Thirty SR and 18 HR patients received intensified chemotherapy. Treatment intensification significantly improved EFS in patients with high MRD (94.2% vs. 75.5%, p = 0.04), particularly in post-induction patients with high MRD (90.0% vs. 19.0%, p = 0.035). The difference in survival between rapid early responder (RER) and slow early responder (SER) groups was eliminated after MRD-based intensification. The implementation rates of treatment intensification varied over time (9.1% before 2015, 28.6% during 2016-2019, and 13.9% during 2020-2023), reflecting improved risk stratification and therapy selection.

CONCLUSION

MRD-guided therapy intensification markedly improved survival outcomes in patients with pediatric ALL when combined with risk-based protocols, highlighting the importance of MRD monitoring for optimizing risk-adapted treatment strategies.

摘要

目的

微小残留病(MRD)指导的治疗是儿童急性淋巴细胞白血病(ALL)的全球标准治疗方法。我们评估了MRD驱动的强化治疗以及方案定义的风险组在儿童ALL治疗中的影响。

方法

这项回顾性分析纳入了209例ALL患者(2013年1月至2023年6月期间接受治疗)。在维持期前每个阶段结束时,使用六至八色流式细胞术评估MRD。诱导后治疗根据早期反应、美国国立癌症研究所风险和细胞遗传学确定。高危(HR)患者遵循韩国HR或CCG-1882方案,标准风险(SR)患者遵循改良的COG-AALL0331方案。如果确定流式MRD≥0.1%,则加强治疗。

结果

总体而言,分别有103例和106例患者被分类为SR和HR。5年总生存率(OS)和无事件生存率(EFS)分别为92.5%和84.3%。30例SR患者和18例HR患者接受了强化化疗。治疗强化显著改善了高MRD患者的EFS(94.2%对75.5%,p = 0.04),特别是诱导后高MRD患者(90.0%对19.0%,p = 0.035)。基于MRD的强化治疗后,快速早期反应者(RER)和缓慢早期反应者(SER)组之间的生存差异消除。治疗强化的实施率随时间变化(2015年前为9.1%,2016 - 2019年期间为28.6%,2020 - 2023年期间为13.9%),这反映了风险分层和治疗选择的改善。

结论

MRD指导的治疗强化与基于风险的方案相结合时,显著改善了儿童ALL患者的生存结果,突出了MRD监测对优化风险适应性治疗策略的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c513/12240913/9e581d576b78/44313_2025_85_Fig1_HTML.jpg

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