VCD/IE方案联合阿帕替尼治疗化疗失败进展期尤因肉瘤的回顾性研究

叶挺 范丽 曹如波 彭玲 陈静

叶挺, 范丽, 曹如波, 彭玲, 陈静. VCD/IE方案联合阿帕替尼治疗化疗失败进展期尤因肉瘤的回顾性研究[J]. 中国肿瘤临床, 2023, 50(3): 125-129. doi: 10.12354/j.issn.1000-8179.2023.20220955
引用本文: 叶挺, 范丽, 曹如波, 彭玲, 陈静. VCD/IE方案联合阿帕替尼治疗化疗失败进展期尤因肉瘤的回顾性研究[J]. 中国肿瘤临床, 2023, 50(3): 125-129. doi: 10.12354/j.issn.1000-8179.2023.20220955
Ting Ye, Li Fan, Rubo Cao, Ling Peng, Jing Chen. A retrospective study on VCD/IE regimen combined with apatinib for advanced Ewing sarcoma unresponsive to chemotherapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2023, 50(3): 125-129. doi: 10.12354/j.issn.1000-8179.2023.20220955
Citation: Ting Ye, Li Fan, Rubo Cao, Ling Peng, Jing Chen. A retrospective study on VCD/IE regimen combined with apatinib for advanced Ewing sarcoma unresponsive to chemotherapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2023, 50(3): 125-129. doi: 10.12354/j.issn.1000-8179.2023.20220955

VCD/IE方案联合阿帕替尼治疗化疗失败进展期尤因肉瘤的回顾性研究

doi: 10.12354/j.issn.1000-8179.2023.20220955
基金项目: 本文课题受北京市希思科临床肿瘤学研究基金(编号:Y-HR2016-158)和华中科技大学同济医学院研究型临床医师资助计划资助
详细信息
    作者简介:

    叶挺:专业方向为肉瘤与黑色素瘤研究

    通讯作者:

    陈静 chenjingunion@163.com

A retrospective study on VCD/IE regimen combined with apatinib for advanced Ewing sarcoma unresponsive to chemotherapy

Funds: This work was supported by Beijing CSCO Clinical Oncology Research Fund (No. Y-HR2016-158) and Research Clinician Funding Program of Tongji Medical College, Huazhong University of Science and Technology
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  • 摘要:   目的  评估VCD/IE方案(长春新碱+环磷酰胺+多柔比星与异环磷酰胺+依托泊苷交替)联合阿帕替尼治疗化疗失败进展期尤因肉瘤的疗效与安全性。  方法  回顾性研究2017年1月至2021年12月于华中科技大学同济医学院附属协和医院,接受VCD/IE方案联合阿帕替尼治疗化疗失败的进展期尤因肉瘤11例患者的临床资料。与同期接受阿帕替尼单药治疗的尤因肉瘤患者对比,评估该方案的疗效及安全性。主要观察终点为疾病无进展生存期(progression-free survival,PFS),次要观察终点为客观缓解率(objective response rate,ORR)、疾病控制率(disease control rate,DCR)、总生存时间(overall survival,OS)和不良反应(adverse event,AE)。  结果  共筛选出符合入排标准的联合治疗患者11例,阿帕替尼单药组10例。两组患者中位随访时间分别为19.5个月和14.5个月。其中男性占比分别为72.7%(8/11)和70%(7/10),平均年龄分别为18.1±6.7岁和20.8±15.7岁。VCD/IE方案联合阿帕替尼的ORR、DCR、中位PFS、中位OS分别为27.3%(3/11)、81.8%(9/11)、 6.4个月和10.9个月。阿帕替尼单药治疗的ORR、DCR、中位PFS、中位OS分别为0、62.5%(5/8)、1.8个月和4.1个月。联合用药期间,3~4级AE主要为化疗相关的中性粒细胞减少、贫血、血小板减少、粒缺性发热等,而阿帕替尼相关AE均为1~2级。AE总体可以耐受。  结论  VCD/IE方案联合阿帕替尼治疗化疗失败的进展期尤因肉瘤疗效明显优于阿帕替尼单药,AE可控。

     

  • 图  1  以基线大小为参照达到最佳疗效时肿瘤体积变化瀑布图

    图  2  化疗联合阿帕替尼组和阿帕替尼单药组肿瘤大小相对于基线值随时间的变化趋势

    图  3  化疗联合阿帕替尼组和阿帕替尼单药组的PFS曲线

    图  4  化疗联合阿帕替尼组和阿帕替尼单药组的OS曲线

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出版历程
  • 收稿日期:  2022-06-22
  • 录用日期:  2022-11-04
  • 修回日期:  2022-11-04
  • 网络出版日期:  2023-02-14

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