Zhao Hong-Bin, Qiao Jia-Jia, He Xue-Hua
Department of Blood Transfusion, Shanxi Bethune Hospital, Taiyuan 030001, Shanxi Province, China.
Department of Blood Transfusion, Shanxi Bethune Hospital, Taiyuan 030001, Shanxi Province, China.E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Aug;32(4):1058-1062. doi: 10.19746/j.cnki.issn.1009-2137.2024.04.013.
To analyze the correlation between serum fibronectin 3 (Ficolin-3) levels and early severe bleeding in newly diagnosed acute promyelocytic leukemia (APL) patients.
A total of 125 patients with newly diagnosed APL admitted to Shanxi Bethune Hospital from January 2020 to August 2023 were selected. All patients were given all-trans retinoic acid+arsenic for induction therapy. The severe bleeding events within 30 days of induction therapy (assessed by WHO bleeding score, grade 0, grade 1 and grade 2 were no bleeding or mild bleeding, grade 3 and grade 4 were severe or fatal bleeding) were used as observation endpoints. The serum Ficolin-3 levels was dected by ELISA method, baseline data and other laboratory indicators were counted, and the correlation between serum Ficolin-3 levels and early severe bleeding in newly diagnosed APL patients was analyzed.
23 out of 125 APL patients experienced early severe bleeding during induction therapy, including 13 cases of grade 3 bleeding and 10 cases of grade 4 bleeding. There were 102 cases of non-serious bleeding, including 30 cases of grade 0, 24 cases of grade 1 bleeding, and 48 cases of grade 2 bleeding. The proportion of serum promyelocytes, white blood cell count, and D-D level in the severe bleeding group were significantly higher than those in the non severe bleeding group ( < 0.05), while the levels of PLT and FIB were significantly lower than those in the non-serious bleeding group ( < 0.05). The serum Ficolin-3 levels in the severe bleeding group were significantly lower than those in the non severe bleeding group before treatment, days of treatment, 14 days of treatment, and 30 days of treatment ( < 0.05). Confirmed by point two column correlation, serum Ficolin-3 levels were negatively correlated with early severe bleeding in newly diagnosed APL patients before treatment, 7 days, 14 days, and 30 days after treatment ( values were -0.485, -0.397, -0.304, and -0.183, respectively). The receiver operating characteristic curve (ROC) graph of the subjects was drawn, and the results showed that the area under the curve (AUC) of serum Ficolin-3 levels before treatment and at 7 and 14 days after treatment for predicting early severe bleeding in newly diagnosed APL patients was greater than 0.7, all of which had certain predictive efficacy, and the serum Ficolin-3 level before treatment had the best predictive efficacy.
The serum Ficolin-3 levels in newly diagnosed APL patients are associated with early severe bleeding, and the serum Ficolin-3 levels before treatment have a significant advantage in predicting early severe bleeding in newly diagnosed APL patients.
分析新诊断急性早幼粒细胞白血病(APL)患者血清纤维胶凝蛋白3(Ficolin-3)水平与早期严重出血之间的相关性。
选取2020年1月至2023年8月在山西白求恩医院收治的125例新诊断APL患者。所有患者均接受全反式维甲酸+砷剂诱导治疗。以诱导治疗30天内的严重出血事件(采用WHO出血评分评估,0级、1级和2级为无出血或轻度出血,3级和4级为严重或致命出血)作为观察终点。采用ELISA法检测血清Ficolin-3水平,统计基线数据及其他实验室指标,分析新诊断APL患者血清Ficolin-3水平与早期严重出血的相关性。
125例APL患者中23例在诱导治疗期间发生早期严重出血,其中3级出血13例,4级出血10例。非严重出血102例,包括0级30例、1级出血24例、2级出血48例。严重出血组血清早幼粒细胞比例、白细胞计数及D-D水平显著高于非严重出血组(P<0.05),而PLT及FIB水平显著低于非严重出血组(P<0.05)。严重出血组治疗前、治疗当天、治疗14天及治疗30天血清Ficolin-3水平均显著低于非严重出血组(P<0.05)。经点二列相关证实,新诊断APL患者治疗前、治疗7天、14天及30天血清Ficolin-3水平与早期严重出血呈负相关(r值分别为-0.485、-0.397、-0.304及-0.183)。绘制受试者工作特征曲线(ROC)图,结果显示治疗前及治疗后7天、14天血清Ficolin-3水平预测新诊断APL患者早期严重出血的曲线下面积(AUC)均大于0.7,均具有一定预测效能,其中治疗前血清Ficolin-3水平预测效能最佳。
新诊断APL患者血清Ficolin-3水平与早期严重出血相关,治疗前血清Ficolin-3水平在预测新诊断APL患者早期严重出血方面具有显著优势。