Comparison of the International Consensus and 5th WHO edition classifications of adult myelodysplastic syndromes and acute myeloid leukemia

被引:18
|
作者
Falini, Brunangelo [1 ,2 ,3 ]
Martelli, Maria Paola [1 ,2 ,3 ]
机构
[1] Univ Perugia, Inst Hematol, Perugia, Italy
[2] Univ Perugia, Ctr forHemato Oncol Res CREO, Perugia, Italy
[3] Santa Maria DellaMisericordia Hosp, Perugia, Italy
基金
欧洲研究理事会;
关键词
HEALTH-ORGANIZATION CLASSIFICATION; VARIANT ALLELE FREQUENCY; CLONAL HEMATOPOIESIS; TP53; MUTATIONS; PROGNOSTIC IMPACT; MULTILINEAGE DYSPLASIA; CLINICAL-SIGNIFICANCE; POTENTIAL PREDICTOR; MONOSOMAL KARYOTYPE; SOMATIC MUTATIONS;
D O I
10.1002/ajh.26812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several editions of the World Health Organization (WHO) classifications of lympho-hemopoietic neoplasms in 2001, 2008, and 2016 served as the international standard for diagnosis. Since the 4th WHO edition, here referred as WHO-HAEM4, significant clinico-pathological, immunophenotypic, and molecular advances have been made in the field of myeloid neoplasms, which have contributed to refine diagnostic criteria, to upgrade entities previously defined as provisional and to identify new entities. This process has resulted in two recent classification proposals of myeloid neoplasms: the International Consensus Classification (ICC) and the 5th edition of the WHO classification (WHO-HAEM5). In this paper, we review and compare the two classifications in terms of diagnostic criteria and entity definition, with a focus on adult myelodysplastic syndromes/neoplasms (MDS) and acute myeloid leukemia (AML). The goal is to provide a tool to facilitate the work of pathologists, hematologists and researchers involved in the diagnosis and treatment of these hematological malignancies.
引用
收藏
页码:481 / 492
页数:12
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