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2
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Retinoic acid and arsenic trioxide in the treatment of acute promyelocytic leukemia: current perspectives.维甲酸与三氧化二砷治疗急性早幼粒细胞白血病:当前观点
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Acute Promyelocytic Leukemia (APL): Comparison Between Children and Adults.急性早幼粒细胞白血病(APL):儿童与成人的比较
Mediterr J Hematol Infect Dis. 2014 Apr 15;6(1):e2014032. doi: 10.4084/MJHID.2014.032. eCollection 2014.

本文引用的文献

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Huang ME, Ye YC, Chen SR, et al. Use of all-trans retinoic acid in the treatment of acute promyelocytic leukemia. Blood. 1988;72(2):567-572.黄玫,叶玉成,陈赛娟等。全反式维甲酸治疗急性早幼粒细胞白血病。《血液》。1988年;72(2):567 - 572。
Blood. 2016 Dec 29;128(26):3017. doi: 10.1182/blood-2016-11-750182.
2
AIDA 0493 protocol for newly diagnosed acute promyelocytic leukemia: very long-term results and role of maintenance.AIDA 0493 方案治疗初发急性早幼粒细胞白血病:极长期结果和维持治疗的作用。
Blood. 2011 May 5;117(18):4716-25. doi: 10.1182/blood-2010-08-302950. Epub 2011 Mar 8.
3
Front-line treatment of acute promyelocytic leukemia with AIDA induction followed by risk-adapted consolidation for adults younger than 61 years: results of the AIDA-2000 trial of the GIMEMA Group.AIDA 诱导后适应风险的巩固治疗用于年龄小于 61 岁的成人急性早幼粒细胞白血病的一线治疗:意大利血液与骨髓移植组 AIDA-2000 试验的结果。
Blood. 2010 Oct 28;116(17):3171-9. doi: 10.1182/blood-2010-03-276196. Epub 2010 Jul 19.
4
Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: long-term follow-up data.三氧化二砷单药治疗初发急性早幼粒细胞白血病:长期随访数据。
J Clin Oncol. 2010 Aug 20;28(24):3866-71. doi: 10.1200/JCO.2010.28.5031. Epub 2010 Jul 19.
5
Risk-adapted treatment of acute promyelocytic leukemia based on all-trans retinoic acid and anthracycline with addition of cytarabine in consolidation therapy for high-risk patients: further improvements in treatment outcome.基于全反式维甲酸和蒽环类药物联合阿糖胞苷巩固治疗高危患者的急性早幼粒细胞白血病的风险适应性治疗:治疗结果的进一步改善。
Blood. 2010 Jun 24;115(25):5137-46. doi: 10.1182/blood-2010-01-266007. Epub 2010 Apr 14.
6
Very long-term outcome of acute promyelocytic leukemia after treatment with all-trans retinoic acid and chemotherapy: the European APL Group experience.全反式维甲酸和化疗治疗急性早幼粒细胞白血病的极长期疗效:欧洲 APL 组的经验。
Blood. 2010 Mar 4;115(9):1690-6. doi: 10.1182/blood-2009-07-233387. Epub 2009 Dec 17.
7
How I treat acute promyelocytic leukemia.我如何治疗急性早幼粒细胞白血病。
Blood. 2009 Dec 10;114(25):5126-35. doi: 10.1182/blood-2009-07-216457.
8
Improved outcome of acute promyelocytic leukemia with high WBC counts over the last 15 years: the European APL Group experience.过去15年中高白细胞计数的急性早幼粒细胞白血病患者预后改善:欧洲急性早幼粒细胞白血病协作组的经验
J Clin Oncol. 2009 Jun 1;27(16):2668-76. doi: 10.1200/JCO.2008.18.4119. Epub 2009 May 4.
9
Long-term efficacy and safety of all-trans retinoic acid/arsenic trioxide-based therapy in newly diagnosed acute promyelocytic leukemia.全反式维甲酸/三氧化二砷疗法在新诊断急性早幼粒细胞白血病中的长期疗效与安全性
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3342-7. doi: 10.1073/pnas.0813280106. Epub 2009 Feb 18.
10
Effective treatment of acute promyelocytic leukemia with all-trans-retinoic acid, arsenic trioxide, and gemtuzumab ozogamicin.全反式维甲酸、三氧化二砷和吉妥珠单抗奥唑米星对急性早幼粒细胞白血病的有效治疗。
J Clin Oncol. 2009 Feb 1;27(4):504-10. doi: 10.1200/JCO.2008.18.6130. Epub 2008 Dec 15.

初诊急性早幼粒细胞白血病。

Newly diagnosed acute promyelocytic leukemia.

机构信息

Unità Operativa Complessa di Ematologia, Trapianto di cellule staminali, Medicina trasfusionale e Terapia cellulare. Università Campus Bio-Medico, Roma, Italy.

出版信息

Mediterr J Hematol Infect Dis. 2011;3(1):e2011064. doi: 10.4084/MJHID.2011.064. Epub 2011 Dec 20.

DOI:10.4084/MJHID.2011.064
PMID:22220261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3248341/
Abstract

Acute promyelocytic leukemia (APL) represents a medical emergency with a high rate of early mortality. As a consequence, as soon as the diagnosis is suspected based upon cytologic criteria, it is necessary to start all- trans retinoic acid (ATRA) treatment without delay. For patients with newly diagnosed APL, induction therapy with ATRA plus anthracycline based chemotherapy is recommended. At present the combination of arsenic trioxide plus ATRA should be considered for patients who are not candidates for anthracycline-based therapy. For pediatric and adult patients with APL aged < 60 years who achieve a CR with induction, I recommend 3 intensive courses of consolidation chemotherapy associated to ATRA, targeted on the basis of the risk group at diagnosis. In patients treated with a very intensive consolidation chemotherapy maintenance treatment can be omitted. However If a maintenance treatment has to be adopted I suggest the use of intermittent ATRA for 15 days every 3 months for a period of 2 years, rather than ATRA associated to chemotherapy. Moreover, taking into account the medical literature, a reduced dosage of ATRA ( 25 mg/m(2)) in pediatric patients and a consolidation chemotherapy of reduced intensity in elderly patients is recommended. Furthermore, in order to maximize survival, careful attention should be reserved to the coagulopathy and to the appearance of the differentiation syndrome. Finally, PCR for the PML/RARA fusion gene on a bone marrow specimen every three months for two years, and then every six months for additional three years are needed during the follow-up.

摘要

急性早幼粒细胞白血病(APL)是一种具有高早期死亡率的医学急症。因此,一旦根据细胞学标准怀疑诊断,就必须立即开始全反式维甲酸(ATRA)治疗。对于新诊断的 APL 患者,推荐使用 ATRA 加蒽环类药物化疗进行诱导治疗。目前,对于不适合蒽环类药物治疗的患者,应考虑使用三氧化二砷加 ATRA 的联合治疗。对于年龄 < 60 岁且诱导缓解后达到完全缓解的儿科和成人 APL 患者,我建议根据诊断时的风险组,进行 3 个强化巩固化疗联合 ATRA。对于接受非常强化巩固化疗的患者,可以省略维持治疗。然而,如果必须采用维持治疗,我建议每 3 个月使用 ATRA(15 天)进行间歇性治疗,持续 2 年,而不是 ATRA 联合化疗。此外,根据医学文献,建议在儿科患者中使用较低剂量的 ATRA(25mg/m²),并在老年患者中进行强度降低的巩固化疗。此外,为了最大限度地提高生存率,应仔细注意凝血功能障碍和分化综合征的出现。最后,在随访期间,需要每 3 个月对骨髓样本进行 PML/RARA 融合基因的 PCR 检测,持续 2 年,然后每 6 个月检测 3 年。