Author:
Luz Arana-Luna Luara,Antonio De la Peña Celaya José,Hernández-Ruiz Eleazar,Luis Alvarez Vera José,Eugenia Espitia Ríos María,Manuel Pérez Zúñiga Juan,Montoya Jiménez Leire,Pelayo Mena Cynthia,Alvarado-Ibarra Martha
Abstract
Acute myeloid leukemia (AML) represents a significant therapeutic challenge despite progress; also, the management of patients aged below 60 remains challenging. This demographic typically exhibits a heterogeneous response to treatment, influenced by genetic, molecular, and clinical factors. The cornerstone of AML treatment encompasses induction chemotherapy aimed at achieving complete remission, followed by consolidation therapy to eliminate residual disease. Recent advances have introduced targeted therapies, such as FLT3 inhibitors and IDH1/2 inhibitors, which have shown promise in improving outcomes in specific patient subsets with relevant genetic mutations. Allogeneic hematopoietic stem cell transplantation (HSCT) remains a critical component for those at high risk of relapse, offering a potential cure in the post-remission phase. The decision-making process for treatment is complex, necessitating a personalized approach based on cytogenetic and molecular aberrations.