医学
急性早幼粒细胞白血病
重症监护医学
髓系白血病
造血干细胞移植
疾病
拉丁美洲
流行病学
移植
免疫学
内科学
政治学
生物化学
维甲酸
化学
法学
基因
作者
Andrés Gómez‐De León,Roberta Demichelis‐Gómez,Abel Costa-Neto,David Gómez‐Almaguer,Eduardo Magalhães Rego
出处
期刊:Hematology
[Informa]
日期:2023-01-06
卷期号:28 (1)
被引量:2
标识
DOI:10.1080/16078454.2022.2158015
摘要
to review the current diagnostic and therapeutic landscape of AML in Latin America as a reflection of other low- and middle-income countries and regions of the world. Encompassing both acute promyelocytic and non-promyelocytic disease types.We reviewed the literature and study registries concerning epidemiological features of patients with AML/APL treated in Latin America, as well as evaluated diagnostic and genetic stratification and patient fitness assessment challenges, the importance of early mortality and supportive care capacity, intensive and non-intensive chemotherapy alternatives, consolidation, and maintenance strategies including novel agents and hematopoietic stem cell transplantation.Although most of the current technologies and treatment options are available in the region, a significant fraction of patients have only limited access to them. In addition, mortality in the first weeks from diagnosis is higher in the region compared to developed countries.Disparities in access to technologies, supportive care capacity, and availability of novel agents and HSCT hinder results in our region, reflecting barriers common to other LMICs. Recent developments in the diagnosis and treatment of this disease must be implemented through education, collaborative clinical research, and advocacy to improve outcomes.
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