首都医科大学学报 ›› 2025, Vol. 46 ›› Issue (3): 420-426.doi: 10.3969/j.issn.1006-7795.2025.03.004

• 肿瘤研究进展:从基础到临床 • 上一篇    下一篇

海曲泊帕治疗生殖细胞肿瘤治疗后血小板减少症的临床疗效分析

李亚伟1,杨守博2,尹硕2,李文斌2,陈峰2*   

  1. 1.贵阳市第二人民医院肿瘤科,贵州贵阳 550000;2.首都医科大学附属北京天坛医院肿瘤综合治疗中心神经肿瘤综合治疗病区,北京 100070
  • 收稿日期:2025-02-27 出版日期:2025-06-21 发布日期:2025-06-24
  • 通讯作者: 陈峰 E-mail:chenfeng406@sina .com
  • 基金资助:
    国家重点研发计划项目(2021YFF0901404)。

Clinical efficacy analysis of hetrombopag in the treatment of cancer therapy included thrombocytopenia for germ cell tumors

Li Yawei1, Yang Shoubo2,  Yin Shuo2, Li Wenbin2, Chen Feng2*   

  1. 1.Department of Oncology, The Second People's Hospital of Guiyang City, Guiyang 550000, Guizhou Province, China; 2. Department of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China
  • Received:2025-02-27 Online:2025-06-21 Published:2025-06-24
  • Supported by:
    This study was supported by the National Key Research & Development Program of China (2021YFF0901404).

摘要: 目的  分析联合海曲泊帕治疗生殖细胞肿瘤治疗后血小板减少症 (cancer therapy induced thrombocytopenia,CTIT) 的疗效及安全性。方法  收集并分析2021年1月至2024年3月收治的颅内生殖细胞肿瘤化学药物治疗(以下简称化疗)后合并CTIT≥Ⅲ级患者的资料,筛选符合入组标准的患者33例,其中研究组为口服海曲泊帕联合皮下注射重组人血小板生成素(recombinant human thrombopoietin, rhTPO)或白细胞介素-11(interleukin-11, IL-11)治疗,对照组为皮下注射rhTPO或IL-11,对比两组患者治疗前后血小板计数、升血小板应答率、平均起效时间、下一周期治疗延长发生率的差异,并统计两组不良反应。结果  两组患者在接受上述治疗后,血小板计数均有提高,用药后第1、2、3天血小板计数升高两组之间差异无统计学意义(P>0.05),研究组用药后第(7±3)天血小板升高计数对比对照组有显著升高,差异有统计学意义(P<0.05),随着时间延长升血小板应答率有所升高。研究组用药平均起效时间3(3,5)d,对照组平均起效时间为4(3,7)d,差异无统计学意义(P>0.05)。研究组导致下一周期治疗时间延长发生率为54.5%,对照组下一周期治疗时间延长发生率为81.8%,两组之间差异无统计学意义(P>0.05)。研究组有2名患者出现轻度可逆性肝功能异常。结论  海曲泊帕联合rhTPO或IL-11治疗颅内生殖细胞肿瘤化疗后CTIT症的疗效可靠,可显著提升血小板计数,不良反应可耐受。

关键词: 海曲泊帕, 颅内生殖细胞肿瘤, 肿瘤治疗后血小板减少症, 重组人血小板生成素, 白细胞介素-11

Abstract: Objective  To retrospectively analyze the efficacy and safety of combined hetrombopag in the treatment of cancer therapy induced thrombocytopenia (CTIT) after chemotherapy for germ cell tumors. Methods  The data of patients with CTIT ≥ grade Ⅲ combined with chemotherapy for intracranial germ cell tumors admitted from January 2021 to March 2024 were collected and analyzed, and 33 patients met the enrollment criteria. The patients in the study group were treated with oral hetrombopag combined with subcutaneous injections of recombinant human thrombopoietin (rhTPO) or interleukin-11 (IL-11), and those in the control group were treated with subcutaneous injections of rhTPO or IL-11. The differences of the two groups of patients in platelet counts, platelet-raising response rate, mean onset of action time, and prolongation of the next cycle of treatment before and after the treatment were compared to each other, and the adverse reactions of the two groups were also counted. Results  The platelet counts of patients in both groups were improved post-treatment, with no statistical significance between the two groups for platelet count elevation on days d1, d2, and d3 of the medication (P>0.05). The platelet elevation counts of the study group were significantly elevated on day d(7 ± 3) after the medication compared with the control group, with a statistically significant difference (P<0.05), and the rate of platelet elevation response increased with time prolongation. The mean time to onset of drug administration was 3(3,5) in the study group and 4(3,7)in the control group, with no statistically significant difference (P>0.05). The incidence of prolongation of the time to the next cycle of treatment was 54.5% in the study group and 81.8% in the control group, and the difference between the two groups was not statistically significant (P>0.05). Two patients in the study group developed mild reversible liver function abnormalities. Conclusion  The efficacy of hetrombopag combined with subcutaneous injection of t rhTPO or IL-11 in the treatment of thrombocytopenia after chemotherapy for intracranial germ cell tumors is reliable, and it can significantly elevate platelet counts with tolerable adverse effects.

Key words: hetrombopag, intracranial germ cell tumors, cancer therapy induced thrombocytopenia, recombinant human thrombopoietin, interleukin-11.

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