[单核细胞计数在非重度再生障碍性贫血患者中的预后意义]。

Q4 Medicine
Xue-Dong Shi, Li Han, Shu-Qi Wang, Qiu-Shuang Wang, Zhen-Yu Li, Kai-Lin Xu, Hai Cheng
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引用次数: 0

摘要

目的:探讨外周血绝对单核细胞计数(AMC)在非严重再生障碍性贫血(NSAA)患者中的预后价值。方法:回顾性分析2008年4月至2020年9月在徐州医科大学附属医院就诊的178例NSAA患者,根据受试者的受试者工作特征曲线确定外周血AMC的最佳临界值,将其分为低AMC组(48例)和正常AMC组(130例),比较两组患者临床特征的差异。Kaplan-Meier分析总生存期(OS)和无进展生存期(PFS)。采用单因素和多因素Cox回归分析确定AMC的独立预后价值。结果178例NSAA患者中,男性105例(59.0%),女性73例(41.0%),中位年龄31(18-87)岁,中位随访时间58个月(范围:6个月~ 175个月),中位AMC为0.15×109/L[范围:(0.01-0.59)×109/L]。低AMC组粒细胞比例(27.5% vs 36.0%, P < 0.05)、成熟单核细胞比例(1% vs 2%, P < 0.05)低于正常AMC组;低AMC组成熟淋巴细胞比例高于正常AMC组(54% vs 50%, P < 0.05)。但两组红细胞比例及红细胞分期差异无统计学意义(P < 0.05)。正常AMC组CR (27.7% vs 10.4%)和ORR (75.4% vs 56.3%)均高于低AMC组。与低AMC组相比,正常AMC组AA患者的5年OS (98.5% vs 86.9%, P < 0.01)和5年PFS (86.0% vs 58.9%, P < 0.01)优于低AMC组。正常AMC组患者10年生存率高于低AMC组(98.5% vs 60.5%,P < 0.01)。单因素分析显示,年龄、网织网细胞计数、AMC9/L、骨髓成熟单核细胞比例与患者生存率相关。多因素Cox回归分析显示,单核细胞计数减少不是NSAA患者预后不良的独立因素(HR =4.474,95%CI:0.508 ~ 44.390; P =0.172)。结论:初诊时AMC低并不是NSAA患者的独立预后因素,但仍提示AMC具有潜在的预后价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prognostic Significance of Monocyte Count in Patients with Non-Severe Aplastic Anemia].

Objective: To investigate the prognostic value of peripheral blood absolute monocyte count(AMC) in non-severe aplastic anaemia(NSAA) patients.

Methods: 178 patients with NSAA who attended the Affiliated Hospital of Xuzhou Medical University from April 2008 to September 2020 were retrospectively analyzed, and the optimal cut-off value of peripheral blood AMC was determined by the receiver operating characteristic curve of the subjects, and they were divided into low AMC group (48 patients) and normal AMC group (130 patients), and the differences in clinical characteristics between the two groups were compared. Overall survival(OS) and progression-free survival(PFS) were analyzed by Kaplan-Meier. Univariate and multivariate Cox regression analysis were used to determine the independent prognostic value of AMC.

Results: Among 178 NSAA patients, 105(59.0%) were male and 73(41.0%) were female, with a median age of 31(18-87) years old, a median follow-up time of 58 months (range: 6 months-175 months), and a median AMC of 0.15×109/L [range: (0.01-0.59)×109/L)]. The proportion of granulocytes (27.5% vs 36.0%, P < 0.05), and the proportion of mature monocytes (1% vs 2%, P < 0.05) in the low AMC group were lower than that in the normal AMC group; the proportion of mature lymphocytes in the low AMC group was higher than that in the normal AMC group (54% vs 50%, P < 0.05). However, there was no significantly different in the proportion of erythropoietic cells and stages of the erythropoietic cells between the two groups ( P >0.05). CR (27.7% vs 10.4%) and ORR (75.4% vs 56.3%) in the normal AMC group were higher than that in the low AMC group. Compared with patients in the low AMC group, AA patients in the normal AMC had better 5-year OS (98.5% vs 86.9%, P < 0.01), and the 5-year PFS (86.0% vs 58.9%, P < 0.01). Also, the 10-year survival rate of patients in the normal AMC group was higher than that in the low AMC group (98.5% vs 60.5%,P < 0.01). Univariate analysis showed that age, reticulocyte count, AMC<0.1×109/L and the proportion of bone marrow mature monocytes were related with patients survival. Multivariate Cox regression analysis showed that monocyte count reduction was not an independent poor prognostic factor in NSAA patients (HR =4.474,95%CI :0.508-44.390; P =0.172).

Conclusion: Low AMC level at initial diagnosis is not an independent prognostic factor for NSAA patients, but still suggest potential prognostic value of AMC.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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