Advances in the Diagnosis and Treatment of Pediatric Acute Lymphoblastic Leukemia

被引:141
作者
Inaba, Hiroto [1 ,2 ]
Pui, Ching-Hon [1 ,2 ]
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, Memphis, TN 38105 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Pediat, Memphis, TN 38163 USA
基金
美国国家卫生研究院;
关键词
acute lymphoblastic leukemia; pediatric; advances; diagnosis; treatment; MINIMAL RESIDUAL DISEASE; RECEPTOR T-CELLS; HIGH-RISK; INTRACHROMOSOMAL AMPLIFICATION; INOTUZUMAB OZOGAMICIN; PROGNOSTIC IMPORTANCE; THERAPEUTIC TARGET; GENOMIC LANDSCAPE; FREE SURVIVAL; YOUNG-ADULTS;
D O I
10.3390/jcm10091926
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The outcomes of pediatric acute lymphoblastic leukemia (ALL) have improved remarkably during the last five decades. Such improvements were made possible by the incorporation of new diagnostic technologies, the effective administration of conventional chemotherapeutic agents, and the provision of better supportive care. With the 5-year survival rates now exceeding 90% in high-income countries, the goal for the next decade is to improve survival further toward 100% and to minimize treatment-related adverse effects. Based on genome-wide analyses, especially RNA-sequencing analyses, ALL can be classified into more than 20 B-lineage subtypes and more than 10 T-lineage subtypes with prognostic and therapeutic implications. Response to treatment is another critical prognostic factor, and detailed analysis of minimal residual disease can detect levels as low as one ALL cell among 1 million total cells. Such detailed analysis can facilitate the rational use of molecular targeted therapy and immunotherapy, which have emerged as new treatment strategies that can replace or reduce the use of conventional chemotherapy.
引用
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页数:24
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