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初诊t(8;21)急性髓系白血病中白血病干细胞相关抗原的表达特征及预后意义

OBJECTIVE: To investigate the characteristic and prognostic significance of leukemia stem cells associated antigens expressions including CD34, CD38, CD123, CD96 and TIM-3 in t(8;21) AML. METHODS: Bone marrow samples of 47 t(8;21) AML patients were collected at diagnosis from October 2015 to April 2...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364990/
https://www.ncbi.nlm.nih.gov/pubmed/31775482
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.10.007
Descripción
Sumario:OBJECTIVE: To investigate the characteristic and prognostic significance of leukemia stem cells associated antigens expressions including CD34, CD38, CD123, CD96 and TIM-3 in t(8;21) AML. METHODS: Bone marrow samples of 47 t(8;21) AML patients were collected at diagnosis from October 2015 to April 2018 in Peking University Peoples' Hospital, then flow cytometry method was performed to detect the expression frequencies of CD34, CD38, CD123, CD96 and TIM-3 to analyze the relationship between leukemia stem cells associated antigens expressions and relapse. RESULTS: Of 47 t(8;21) AML patients tested, the median percentages of CD34(+)CD38(−), CD34(+) CD38(−)CD123(+), CD34(+)CD38(−) CD96(+) and CD34(+) CD38(−) TIM-3(+) cells among nucleated cells were 2.37%, 0.24%, 0.27% and 0.06%, respectively. All the frequencies of CD34(+)CD38(−), CD34(+)CD38(−)CD123(+), CD34(+)CD38(−)CD96(+) and CD34(+) CD38(−)TIM-3(+)cells had no impact on the achievement of CR after the first course of induction. All higher frequencies of CD34(+)CD38(−), CD34(+)CD38(−)CD123(+), CD34(+)CD38(−)CD96(+) cells were related to higher 2-year CIR rate. Whereas, the frequency of CD34(+) CD38(−) TIM-3(+) cells had no impact on CIR rate. Both high frequency of CD34(+) CD38(−) cells and the high level of minimal residual diseases (patients with <3-log reduction in the RUNX1-RUNX1T1 transcript level after the second consolidation therapy) were independent poor prognostic factors of CIR[P=0.025, HR=6.9 (95%CI1.3–37.4) ; P=0.031, HR=11.1 (95%CI 1.2–99.2) ]. CONCLUSION: Different leukemia stem cells associated antigens had distinct prognostic significance in t(8;21) AML. High frequencies of CD34(+) CD38(−), CD34(+) CD38(−) CD123(+) and CD34(+)CD38(−)CD96(+) cells at diagnosis predicted relapse in patients with t(8;21) AML.