期刊论文详细信息
Revista Brasileira de Hematologia e Hemoterapia
Risk stratification for indolent lymphomas
Abrahão Elias Hallack Neto2  Renata Oliveira Costa1  Angelo Atalla2  Frederico Luiz Dulley1  Dalton Alencar Fischer Chamone1  Juliana Pereira1 
[1] ,Universidade Federal de Juiz de Fora - UFJF Faculdade de Medicina Juiz de Fora MG ,Brasil
关键词: Lymphoma;    non-Hodgkin;    Prognosis;    Treatment outcome;    Biologic markers;    Lymphoma;    B-cell;    Lymphoma;    follicular;    Linfoma não Hodgkin;    Prognóstico;    Resultado de tratamento;    Marcadores biológicos;    Linfoma de células B;    Linfoma folicular;   
DOI  :  10.1590/S1516-84842010000500015
来源: SciELO
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【 摘 要 】

Indolent B-cell lymphomas account for approximately 40% of all non-Hodgkin lymphomas (NHLs). Advances in technology have contributed to improvements in the diagnosis and classification of indolent non-Hodgkin lymphomas. Follicular Lymphomas are the most common although the frequency varies significantly throughout the world. The description of the Follicular Lymphoma International Prognostic Index (FLIPI) was an important step in identifying patient subgroups, but its use in the clinical practice has not been established yet. The use of a larger number of paraffin active monoclonal antibodies for immunohistochemistry, molecular cytogenetic studies including standard cytogenetics, multi-color fluorescence in-situ hybridization (FISH), polymerase chain reaction and locus-specific fluorescence insitu hybridization as well as developments in high-resolution techniquesincluding microarray gene expression profiling allow more accurate diagnosis andprecise definition of biomarkers of value in risk stratification. The identification ofdiseasespecific gene lists resulting from expression profiling provides a number ofpotential protein targets that can be validated using immunohistochemistry. Analysesof gene expression profiles or constitutive gene variations may also provide additional insight for prognostication in the near future. A comprehensive understanding of the biology of these distinct lymphoid tumors will allow us to identify novel diseaserelated genes and should facilitate the development of improved diagnosis, outcome prediction, and personalized approaches to treatment.

【 授权许可】

CC BY-NC-ND   
 All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License

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