Your browser doesn't support javascript.
loading
Relationship between Immune Differentiation Antigen and Minimal Residual Disease in Childhood B-ALL / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1301-1308, 2018.
Artigo em Chinês | WPRIM | ID: wpr-689939
ABSTRACT
<p><b>OBJECTIVE</b>To determine whether immune differentiation antigen is related with clinical features and minimal residual disease (MRD) in childhood B-cell precursor acute lymphoblastic leukemia (B-ALL), who were treated with CCCG-ALL-2015 protocol.</p><p><b>METHODS</b>A retrospective analysis was conducted in 132 B-ALL children, Multiparametric flow cytometry was used to analyze the immunophenotypes. The children were divided into 2 groups by MRD>0.1% on d 19 and / or d 46 after chemotherapy. The Wilcoxon rank-sum test and χ test were used for the comparison between groups, and P<0.05 was considered statistically significant.</p><p><b>RESULTS</b>CD19 (100%), CD22 (99.3%) and cCD79a (97.9%) were specific markers for patients with B-ALL, the CD13 and CD33 were mainly cross myeloid antigen. The significant differences were found between CD45 and CD45 in WBC counts when being firstly diagnosed (Z=6.845, P<0.01), risk stratification (χ=8.260, P<0.05) and prednisone poor responder (χ=18.420, P<0.01). Significant differences were found between CD10 and CD10 in age (Z=6.253, P<0.05), risk stratification (χ=6.699, P<0.05) and MRD (χ=4.951, P<0.05).</p><p><b>CONCLUSION</b>In CCCG-ALL-2015 protocol, the CD10 relates with the early MRD, suggesting a better prognosis, and reducing the adverse effects of CD20 and cross myeloid antigen on prognosis.</p>
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Tipo de estudo: Guia de Prática Clínica Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2018 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Tipo de estudo: Guia de Prática Clínica Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2018 Tipo de documento: Artigo