新诊断的急性早幼粒细胞白血病的无化疗方法:口服三氧化二砷/全反式维甲酸/抗坏血酸是答案吗?

IF 2.3 4区 医学 Q2 HEMATOLOGY Expert Review of Hematology Pub Date : 2024-10-01 Epub Date: 2024-08-12 DOI:10.1080/17474086.2024.2391098
Harinder Gill
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引用次数: 0

摘要

简介:急性早幼粒细胞白血病(APL)是急性髓性白血病的一种独特形式,其特征是存在 t(15;17)(q24;21)和 PML:RARA 基因融合。静脉注射三氧化二砷(i.v.-ATO)和全反式维甲酸(ATRA)大大提高了 APL 的治愈率。香港的研究人员发明了三氧化二砷口服制剂(口服三氧化二砷),并证实其生物利用度与静脉注射三氧化二砷相当。大量研究证实,在一线治疗和复发治疗中,以口服 ATO 为基础的治疗方案具有安全性和有效性:讨论了在一线和复发情况下开发基于口服ATO的APL治疗方案的各个方面。讨论了口服ATO治疗方案的短期和长期安全性和有效性。重点介绍了口服ATO联合ATRA和抗坏血酸(AAA)在 "无化疗 "诱导中的一线应用:专家意见:在APL中使用以口服ATO为基础的治疗方案的现有数据支持使用口服ATO作为静脉注射ATO的替代方案,从而以更方便、更经济的方法治疗APL。
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Chemotherapy-free approaches to newly-diagnosed acute promyelocytic leukaemia: is oral-arsenic trioxide/all-trans retinoic acid/ascorbic acid the answer?

Introduction: Acute promyelocytic leukemia (APL) is a distinct form of acute myeloid leukemia characterized by the presence of t(15;17)(q24;21) and the PML:RARA gene fusion. Frontline use of intravenous arsenic trioxide (i.v.-ATO) and all-trans retinoic acid (ATRA) has vastly improved cure rates in APL. Researchers in Hong Kong invented the oral formulation of ATO (oral-ATO) and have confirmed a bioavailability comparable to i.v.-ATO. A plethora of studies have confirmed the safety and efficacy of oral-ATO-based regimens in the frontline and relapsed setting.

Areas covered: Aspects on the development of oral-ATO-based regimens for APL in the frontline and relapsed setting are discussed. The short-term and long-term safety and efficacy of oral-ATO-based regimens are discussed. The frontline use of oral-ATO in combination with ATRA and ascorbic acid (AAA) induction in a 'chemotherapy-free' is highlighted.

Expert opinion: Current and ongoing data on the use of oral-ATO-based regimens in APL support the use of oral-ATO as an alternative to i.v.-ATO allowing a more convenient and economical approach to the management of APL.

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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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