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Leuk Lymphoma. 2019 Mar;60(3):711-719. doi: 10.1080/10428194.2018.1504941. Epub 2018 Nov 8.
2
Risk-adapted treatment of acute promyelocytic leukemia: results from the International Consortium for Childhood APL.急性早幼粒细胞白血病的风险适应性治疗:来自国际儿童急性早幼粒细胞白血病联盟的研究结果。
Blood. 2018 Jul 26;132(4):405-412. doi: 10.1182/blood-2018-03-836528. Epub 2018 May 22.
3
Difference in causes and prognostic factors of early death between cohorts with de novo and relapsed acute promyelocytic leukemia.初发和复发急性早幼粒细胞白血病队列早期死亡原因及预后因素的差异。
Ann Hematol. 2018 Mar;97(3):409-416. doi: 10.1007/s00277-017-3216-2. Epub 2017 Dec 30.
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Retinoic acid and arsenic trioxide sensitize acute promyelocytic leukemia cells to ER stress.维甲酸和三氧化二砷使急性早幼粒细胞白血病细胞对 ER 应激敏感。
Leukemia. 2018 Feb;32(2):285-294. doi: 10.1038/leu.2017.231. Epub 2017 Aug 4.
5
Maintenance therapy with all-trans retinoic acid and arsenic trioxide improves relapse-free survival in adults with low- to intermediate-risk acute promyelocytic leukemia who have achieved complete remission after consolidation therapy.对于低至中危急性早幼粒细胞白血病成人患者,在巩固治疗后已实现完全缓解的情况下,采用全反式维甲酸和三氧化二砷进行维持治疗可提高无复发生存率。
Onco Targets Ther. 2017 Apr 26;10:2305-2313. doi: 10.2147/OTT.S135013. eCollection 2017.
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[SCMC APL - 2010方案治疗儿童急性早幼粒细胞白血病的临床疗效:44例分析]

[Clinical effect of the SCMC APL-2010 regimen in treatment of acute promyelocytic leukemia in children: an analysis of 44 cases].

作者信息

Wang Zhuo, Shen Shu-Hong, Tang Yan-Jing, Xue Hui-Liang, Hu Wen-Ting, Pan Ci, Tang Jing-Yan, Gu Long-Jun, Chen Jing

机构信息

Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2019 Nov;21(11):1073-1078. doi: 10.7499/j.issn.1008-8830.2019.11.004.

DOI:10.7499/j.issn.1008-8830.2019.11.004
PMID:31753087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7389303/
Abstract

OBJECTIVE

To study the clinical effect of the SCMC APL-2010 regimen in the treatment of acute promyelocytic leukemia (APL) in children.

METHODS

A retrospective analysis was performed for the clinical data of 44 children with APL who received treatment with the SCMC APL-2010 regimen between April 2010 and July 2016. The Kaplan-Meier survival analysis was used to evaluate event-free survival (EFS) rate and overall survival (OS) rate.

RESULTS

Of the 44 children with APL, 42 (95%) achieved a complete remission (CR) after one course of treatment and 1 achieved CR after two courses of treatment, with an overall CR rate of 98%. The 9-year EFS and OS rates were 96%±3% and 97.7%±2.2% respectively. As for adverse events, 41 (93%) had infection, 29 (66%) had granulocyte reduction, 12 (27%, 1 died) had differentiation syndrome, 16 (36%) had liver dysfunction, 12 (27%) had adverse gastrointestinal reactions, and 7 (16%) had QT prolongation, 1 (2%) had orchitis, and no secondary neoplasm was observed.

CONCLUSIONS

Children with APL receiving the SCMC APL-2010 regimen have a good prognosis and can achieve a long-term survival, while treatment-related infection is commonly seen.

摘要

目的

研究SCMC APL - 2010方案治疗儿童急性早幼粒细胞白血病(APL)的临床疗效。

方法

对2010年4月至2016年7月期间接受SCMC APL - 2010方案治疗的44例儿童APL患者的临床资料进行回顾性分析。采用Kaplan - Meier生存分析评估无事件生存率(EFS)和总生存率(OS)。

结果

44例儿童APL患者中,42例(95%)在一个疗程后达到完全缓解(CR),1例在两个疗程后达到CR,总CR率为98%。9年EFS率和OS率分别为96%±3%和97.7%±2.2%。不良事件方面,41例(93%)发生感染,29例(66%)出现粒细胞减少,12例(27%,1例死亡)发生分化综合征,16例(36%)出现肝功能障碍,12例(27%)出现胃肠道不良反应,7例(16%)出现QT间期延长,1例(2%)发生睾丸炎,未观察到继发性肿瘤。

结论

接受SCMC APL - 2010方案治疗的儿童APL患者预后良好,可实现长期生存,但治疗相关感染较为常见。