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Straight to the Point-The Novel Strategies to Cure Pediatric AML
被引:10
|作者:
Lejman, Monika
[1
]
Dziatkiewicz, Izabela
[2
]
Jurek, Mateusz
[2
]
机构:
[1] Med Univ Lublin, Fac Pediat 2, Lab Genet Diagnost, A Gebali 6, PL-20093 Lublin, Poland
[2] Med Univ Lublin, Fac Pediat 2, Lab Genet Diagnost, Student Sci Soc, A Gebali 6, PL-20093 Lublin, Poland
关键词:
AML;
pediatric;
targeted therapy;
CAR-T;
ACUTE MYELOID-LEUKEMIA;
ACUTE MYELOGENOUS LEUKEMIA;
ACUTE MEGAKARYOBLASTIC LEUKEMIA;
ACUTE PROMYELOCYTIC LEUKEMIA;
GENE-MUTATIONS;
PROGNOSTIC IMPACT;
NUCLEOPHOSMIN MUTATIONS;
GEMTUZUMAB OZOGAMICIN;
MOLECULAR LANDSCAPE;
ECTOPIC EXPRESSION;
D O I:
10.3390/ijms23041968
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Although the outcome has improved over the past decades, due to improved supportive care, a better understanding of risk factors, and intensified chemotherapy, pediatric acute myeloid leukemia remains a life-threatening disease, and overall survival (OS) remains near 70%. According to French-American-British (FAB) classification, AML is divided into eight subtypes (M0-M7), and each is characterized by a different pathogenesis and response to treatment. However, the curability of AML is due to the intensification of standard chemotherapy, more precise risk classification, improvements in supportive care, and the use of minimal residual disease to monitor response to therapy. The treatment of childhood AML continues to be based primarily on intensive, conventional chemotherapy. Therefore, it is essential to identify new, more precise molecules that are targeted to the specific abnormalities of each leukemia subtype. Here, we review abnormalities that are potential therapeutic targets for the treatment of AML in the pediatric population.
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页数:25
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