临床和实验医学杂志2024,Vol.23Issue(15) :1606-1610.DOI:10.3969/j.issn.1671-4695.2024.15.011

艾曲波帕与利妥昔单抗二线治疗成人原发性免疫性血小板减少症的疗效研究

Observation of curative effect of eltrombopag and rituximab in second-line treatment of adult primary immune thrombocytopenia

张司琪 丰江舟 邢明泉 葛洪峰 孙晓星
临床和实验医学杂志2024,Vol.23Issue(15) :1606-1610.DOI:10.3969/j.issn.1671-4695.2024.15.011

艾曲波帕与利妥昔单抗二线治疗成人原发性免疫性血小板减少症的疗效研究

Observation of curative effect of eltrombopag and rituximab in second-line treatment of adult primary immune thrombocytopenia

张司琪 1丰江舟 1邢明泉 1葛洪峰 1孙晓星1
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作者信息

  • 1. 亳州市人民医院血液内科 安徽 亳州 236800
  • 折叠

摘要

目的 探讨艾曲波帕与利妥昔单抗二线治疗成人原发性免疫性血小板减少症(ITP)的疗效.方法 前瞻性选取2021年5月至2024年3月亳州市人民医院血液内科收治的80例成人ITP患者作为研究对象,按照随机数字表法将其分为对照组和试验组,每组各40例.对照组给予利妥昔单抗治疗,剂量为100 mg,每周静脉滴注1次,分别在第1、8、15、22天进行,持续4周.试验组在对照组基础上给予艾曲波帕治疗,最初剂量为每日25~50 mg的空腹口服给药,根据患者的病情、血小板计数以及药物说明书调整给药剂量,最大剂量为每日75 mg,持续12周.比较两组治疗疗效,比较两组患者治疗前、治疗后7 d、治疗后14 d、治疗后1个月、治疗后3个月的血小板计数,比较两组患者治疗前、治疗后3个月的外周血调节性T细胞(Treg)、辅助性T细胞17(Th17)细胞百分比及Treg/Th17水平,两组的不良反应发生率.结果 试验组治疗总有效率为72.50%,高于对照组(50.00%),差异有统计学意义(P<0.05).治疗后7 d、14 d、1个月、3个月,两组患者的血小板计数均高于治疗前,且试验组治疗后3个月的血小板计数为(133.26±40.23)× 109/L,高于对照组[(85.73±22.24)× 109/L],差异均有统计学意义(P<0.05);试验组与对照组治疗后7 d、14 d、1个月的血小板计数比较,差异均无统计学意义(P>0.05).治疗后3个月,两组患者的外周血Treg及Treg/Th17均高于治疗前,Th17细胞百分比低于治疗前,差异均有统计学意义(P<0.05);且试验组患者治疗后3个月的外周血Treg及Treg/Th17 分别为(5.47±0.50)%、(3.42±0.36),均高于对照组[(5.06±0.49)%、2.89±0.40],Th17 细胞百分比为(1.60±0.11)%,低于对照组[(1.75±0.16)%],差异均有统计学意义(P<0.05).对照组的总不良反应发生率(17.50%)与试验组(27.50%)比较,差异无统计学意义(P>0.05).结论 艾曲波帕与利妥昔单抗二线治疗成人ITP疗效显著,可提高患者的血小板计数,改善患者的免疫调节状态,安全性良好.

Abstract

Objective To explore the efficacy of second-line treatment with eltrombopag and rituximab in adult primary immune throm-bocytopenia(ITP).Methods A total of 80 adult ITP patients admitted to the Department of Hematology,Bozhou People's Hospital from May 2021 to March 2024 were prospectively selected as the research objects.They were divided into the control group and the experimental group ac-cording to the random number table method,with 40 cases in each group.The control group was given rituximab treatment,the dose was 100 mg and was administered intravenously once a week on days 1,8,15,and 22,continuous for 4 weeks.The experimental group was treated with el-trombopag on the basis of the control group,the initial dose was 25 to 50 mg per day of fasting oral administration,and the maximum dose was 75 mg per day according to the patient's condition,platelet count and drug instructions,continuous for 12 weeks.The therapeutic effect of the two groups was compared,the platelet counts before treatment,7 d,14 d,1 month and 3 months after treatment,and the percentage of peripheral blood regulatory T cells(Treg)and helper T cell 17(Th17)and Treg/Th17 levels were compared between the two groups before treatment and 3 months after treatment,the incidence of adverse reactions of the two groups were compared.Results The total effective rate of treatment in the ex-perimental group was 72.50%,which was higher than that in the control group(50.00%),and the difference was statistically significant(P<0.05).At 7 d,14 d,1 month and 3 months after treatment,the platelet counts of the two groups were higher than those before treatment,and the platelet count of the experimental group at 3 months after treatment was(133.26±40.23)× 109/L,which was higher than that of the control group[(85.73±22.24)× 109/L],the differences were statistically significant(P<0.05);there were no significant differences in platelet count between the experimental group and the control group at 7 days,14 days and 1 month after treatment(P>0.05).The peripheral blood Treg and Treg/Th17 in the two groups at 3 months after treatment were higher than those before treatment,and the percentage of Th17 cells in the two groups was lower than that before treatment,the differences were statistically significant(P<0.05).The peripheral blood Treg and Treg/Th17 in the experimental group at 3 months after treatment were(5.47±0.50)%and(3.42±0.36),respectively,which were higher than those in the control group[(5.06±0.49)%and 2.89±0.40],and the percentage of Th17 cells in the experimental group was(1.60±0.11)%,which was lower than that in the control group[(1.75±0.16)%],the differences were statistically significant(P<0.05).There was no sig-nificant difference in the total incidence of adverse reactions between the control group(17.50%)and the experimental group(27.50%)(P>0.05).Conclusion The efficacy of second-line treatment with eltrombopag and rituximab in adult primary immune thrombocytopenia is signifi-cant,which can improve the platelet count of patients,improve the immune regulation status of patients,and has good safety.

关键词

艾曲波帕/利妥昔单抗/成人原发性免疫性血小板减少症/疗效

Key words

Eltrombopag/Rituximab/Adult primary immune thrombocytopenia/Curative effect

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基金项目

安徽医科大学青年基金项目(2023xkj090)

出版年

2024
临床和实验医学杂志
首都医科大学附属北京友谊医院

临床和实验医学杂志

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影响因子:1.504
ISSN:1671-4695
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