王雅静,徐竟益,刘影,任志忠,王天霄,汪桠琴,张跃伟.FOLFOX-肝动脉灌注化疗联合靶向及免疫治疗巴塞罗那临床肝癌C期肝细胞癌[J].中国介入影像与治疗学,2022,19(11):687-692
FOLFOX-肝动脉灌注化疗联合靶向及免疫治疗巴塞罗那临床肝癌C期肝细胞癌
FOLFOX hepatic artery infusion chemotherapy combined with targeted therapy and immunotherapy for Barcelona clinic liver cancer stage C hepatocellular carcinoma
投稿时间:2022-05-20  修订日期:2022-07-11
DOI:10.13929/j.issn.1672-8475.2022.11.004
中文关键词:  肝脏肿瘤  肝动脉  化学治疗,肿瘤,局部灌注  分子靶向治疗  免疫治疗
英文关键词:liver neoplasms  hepatic artery  chemotherapy,cancer,regional perfusion  molecular targeted therapy  immunotherapy
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作者单位E-mail
王雅静 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
 
徐竟益 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
 
刘影 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
 
任志忠 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
 
王天霄 清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218
山东大学齐鲁医学院第二医院肝胆外科, 山东 济南 250033 
 
汪桠琴 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
 
张跃伟 清华大学临床医学院, 北京 100084
清华大学附属北京清华长庚医院肝胆胰中心, 北京 102218 
zhangyuewei1121@sina.com 
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中文摘要:
      目的 观察以FOLFOX方案为核心的肝动脉灌注化疗(HAIC)联合靶向及免疫治疗巴塞罗那临床肝癌(BCLC)-C期肝细胞癌(HCC)的效果和安全性。方法 回顾性分析21例接受HAIC联合靶向及免疫治疗的BCLC-C期HCC患者,记录患者总生存期(OS)及无进展生存期(PFS),计算总缓解率(ORR)和疾病控制率(DCR),以及治疗及随访期间不良事件。结果 治疗后ORR、DCR分别为57.14%(12/21)和95.24%(20/21)。随访4~33个月、中位时间15个月,期间13例死于肿瘤进展;中位OS为11.0[95%CI(6.47,15.52)]个月,中位PFS为5.0[95%CI(4.23,5.76)]个月。不良事件中,1~2级较为常见;治疗期间16例出现3级不良事件,其中1例死于免疫相关性肺炎,15例均于下一治疗周期前恢复。结论 FOLFOX-HAIC联合靶向及免疫治疗BCLC-C期HCC安全、有效。
英文摘要:
      Objective To observe the efficacy and safety of FOLFOX regimen based hepatic arterial infusion chemotherapy (HAIC) combined with targeted therapy and immunotherapy for Barcelona clinic liver cancer (BCLC) C stage hepatocellular carcinoma (HCC). Methods Data of 21 BCLC-C HCC patients who underwent HAIC combined with targeted therapy and immunotherapy were retrospectively analyzed. The overall survival (OS) and progression-free survival (PFS) were recorded, and the overall response rate (ORR) and disease control rate (DCR) were calculated. Adverse events occurred during treatment and follow-up periods were recorded. Results ORR and DCR after treatment was 57.14% (12/21) and 95.24% (20/21), respectively. The total follow-up time was 4 to 33 months, with the median time of 15 months, and 13 cases died due to progression. The median OS was 11.0 (95%CI [6.47, 15.52]) months, and the median PFS was 5.0 (95%CI [4.23, 5.76]) months. Adverse events of grade 1 to 2 were common, while 16 cases experienced grade 3 adverse events during treatments, including 1 patient died of immune-associated pneumonia and the other 15 recovered before the next treatment cycle. Conclusion FOXFOL-HAIC combined with targeted therapy and immunotherapy was safe and effective for treating BCLC-C HCC.
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