{"title":"Insights into Acute Myeloid Leukemia: Critical Analysis on its Wide Aspects","authors":"","doi":"10.34091/ajls.3.2.1","DOIUrl":null,"url":null,"abstract":"Acute myeloid leukaemia (AML) is a heterogeneous, most common type of acute leukaemia that involves mutation in haematopoietic and progenitors stem cells (HPSCs) leading to uncontrolled division, self-renewal and differentiation. Though it was untreatable about a half century ago, AML is now considered to be treatable in up to 40% of adults and those who are at or under 60 years of age. For the post-induction treatment, the mutation testing and cytogenetics are still an important prognostic tool. The AML treatment remains unchanged for almost three decades, although the field is advanced with the discovery of new drugs and deep understanding of the disease biology. Still, many people are relapsing and are dying eventually from the disease. This review discusses the broader aspects of AML, reflecting some of the most important and productive areas of research on the subject and was conducted using thoroughly searching databases, including Health Research and Development Information network Plus (HERDIN Plus), google scholar and PubMed to critically analyses the recent advances, available treatments and future prospectives of AML.","PeriodicalId":371643,"journal":{"name":"Abasyn Journal Life Sciences","volume":"351 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Abasyn Journal Life Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34091/ajls.3.2.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Acute myeloid leukaemia (AML) is a heterogeneous, most common type of acute leukaemia that involves mutation in haematopoietic and progenitors stem cells (HPSCs) leading to uncontrolled division, self-renewal and differentiation. Though it was untreatable about a half century ago, AML is now considered to be treatable in up to 40% of adults and those who are at or under 60 years of age. For the post-induction treatment, the mutation testing and cytogenetics are still an important prognostic tool. The AML treatment remains unchanged for almost three decades, although the field is advanced with the discovery of new drugs and deep understanding of the disease biology. Still, many people are relapsing and are dying eventually from the disease. This review discusses the broader aspects of AML, reflecting some of the most important and productive areas of research on the subject and was conducted using thoroughly searching databases, including Health Research and Development Information network Plus (HERDIN Plus), google scholar and PubMed to critically analyses the recent advances, available treatments and future prospectives of AML.
急性髓性白血病(AML)是一种异质性的、最常见的急性白血病类型,涉及造血干细胞和祖干细胞(HPSCs)的突变,导致不受控制的分裂、自我更新和分化。虽然大约半个世纪前AML是无法治疗的,但现在认为高达40%的成年人和60岁以下的人是可以治疗的。对于诱导后治疗,突变检测和细胞遗传学仍然是一个重要的预后工具。尽管随着新药的发现和对疾病生物学的深入了解,AML的治疗方法在近三十年来一直保持不变。尽管如此,许多人仍在复发,最终死于这种疾病。本综述讨论了AML的更广泛方面,反映了该主题研究的一些最重要和最富有成效的领域,并使用全面搜索数据库,包括健康研究与发展信息网络Plus (HERDIN Plus), google scholar和PubMed,以批判性地分析AML的最新进展,可用的治疗方法和未来前景。