Cargando…

成人急性早幼粒细胞白血病预后相关因素分析

OBJECTIVE: To explore the prognostic value of CD34, CD2, CD56 expressions and FLT3-ITD mutation in adults with acute promyelocytic leukemia (APL). METHODS: The immuno-phenotypic and molecular characteristics of 137 adult patients with APL (from January 2010 to March 2016, in Henan Provincial People&...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342290/
https://www.ncbi.nlm.nih.gov/pubmed/28810326
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.07.007
_version_ 1783555433901850624
collection PubMed
description OBJECTIVE: To explore the prognostic value of CD34, CD2, CD56 expressions and FLT3-ITD mutation in adults with acute promyelocytic leukemia (APL). METHODS: The immuno-phenotypic and molecular characteristics of 137 adult patients with APL (from January 2010 to March 2016, in Henan Provincial People's Hospital) were investigated. And the relationships between CD34, CD2, CD56 expressions, FLT3-ITD mutation and the outcomes of high WBC counts at onset, complete remission (CR) rate, early mortality, relapse rate (RR), overall survival (OS), disease free survival (DFS) were explored. RESULTS: ①Among the 137 patients, the positive ratios of CD34, CD2, CD56 expressions and mutation rate of FLT3-ITD were 26.3%, 25.5%, 10.2% and 17.5%, respectively. The morbidities of positive CD34, CD2, CD56 expressions and FLT3-ITD mutation in the high-risk group were 43.2%, 47.7%, 18.2% and 27.3% respectively, while those in the low-/intermediate-risk groups were 18.3%, 15.1%, 6.5% and 12.9%, respectively (P<0.05). ②At a median follow-up of 41 months, the total CR rate of the 137 adults APL patients was 96.9%, early mortality 6.6% and relapse rate 7.3% respectively. And RR of positive CD34 or CD2 expression patients was higher than negative CD34/CD2 expression ones (18.8% vs 3.3%, χ(2)=8.462, P=0.004; 16.1% vs 4.3%, χ(2)=4.382, P=0.028, respectively). In addition, the early mortality of patients with positive CD56 expression or FLT3-ITD mutation was extremely higher than in negative ones (21.4% vs 4.9%, χ(2)=5.610, P=0.018; 16.7% vs 4.4%, χ(2)=4.833, P=0.028, respectively). ③The whole OS and DFS were 88.3% and 84.7%, respectively. Wherein, OS and DFS in patients with CD34(+), CD56(+) or FLT3-ITD mutation were worse (P<0.05). CONCLUSION: Positive CD34, CD2, CD56 expression and FLT3-ITD mutation were latent poor prognostic factors in adults with APL.
format Online
Article
Text
id pubmed-7342290
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Editorial office of Chinese Journal of Hematology
record_format MEDLINE/PubMed
spelling pubmed-73422902020-07-16 成人急性早幼粒细胞白血病预后相关因素分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To explore the prognostic value of CD34, CD2, CD56 expressions and FLT3-ITD mutation in adults with acute promyelocytic leukemia (APL). METHODS: The immuno-phenotypic and molecular characteristics of 137 adult patients with APL (from January 2010 to March 2016, in Henan Provincial People's Hospital) were investigated. And the relationships between CD34, CD2, CD56 expressions, FLT3-ITD mutation and the outcomes of high WBC counts at onset, complete remission (CR) rate, early mortality, relapse rate (RR), overall survival (OS), disease free survival (DFS) were explored. RESULTS: ①Among the 137 patients, the positive ratios of CD34, CD2, CD56 expressions and mutation rate of FLT3-ITD were 26.3%, 25.5%, 10.2% and 17.5%, respectively. The morbidities of positive CD34, CD2, CD56 expressions and FLT3-ITD mutation in the high-risk group were 43.2%, 47.7%, 18.2% and 27.3% respectively, while those in the low-/intermediate-risk groups were 18.3%, 15.1%, 6.5% and 12.9%, respectively (P<0.05). ②At a median follow-up of 41 months, the total CR rate of the 137 adults APL patients was 96.9%, early mortality 6.6% and relapse rate 7.3% respectively. And RR of positive CD34 or CD2 expression patients was higher than negative CD34/CD2 expression ones (18.8% vs 3.3%, χ(2)=8.462, P=0.004; 16.1% vs 4.3%, χ(2)=4.382, P=0.028, respectively). In addition, the early mortality of patients with positive CD56 expression or FLT3-ITD mutation was extremely higher than in negative ones (21.4% vs 4.9%, χ(2)=5.610, P=0.018; 16.7% vs 4.4%, χ(2)=4.833, P=0.028, respectively). ③The whole OS and DFS were 88.3% and 84.7%, respectively. Wherein, OS and DFS in patients with CD34(+), CD56(+) or FLT3-ITD mutation were worse (P<0.05). CONCLUSION: Positive CD34, CD2, CD56 expression and FLT3-ITD mutation were latent poor prognostic factors in adults with APL. Editorial office of Chinese Journal of Hematology 2017-07 /pmc/articles/PMC7342290/ /pubmed/28810326 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.07.007 Text en 2017年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
成人急性早幼粒细胞白血病预后相关因素分析
title 成人急性早幼粒细胞白血病预后相关因素分析
title_full 成人急性早幼粒细胞白血病预后相关因素分析
title_fullStr 成人急性早幼粒细胞白血病预后相关因素分析
title_full_unstemmed 成人急性早幼粒细胞白血病预后相关因素分析
title_short 成人急性早幼粒细胞白血病预后相关因素分析
title_sort 成人急性早幼粒细胞白血病预后相关因素分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342290/
https://www.ncbi.nlm.nih.gov/pubmed/28810326
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.07.007
work_keys_str_mv AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī
AT chéngrénjíxìngzǎoyòulìxìbāobáixuèbìngyùhòuxiāngguānyīnsùfēnxī