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对于在经动脉化疗栓塞术联合阿帕替尼治疗后出现进展的不可切除肝细胞癌患者,添加卡瑞利珠单抗是有效且安全的。

The addition of camrelizumab is effective and safe among unresectable hepatocellular carcinoma patients who progress after drug-eluting bead transarterial chemoembolization plus apatinib therapy.

作者信息

Wang Manzhou, Sun Limin, Han Xinwei, Ren Jianzhuang, Li Hao, Wang Wenhui, Xu Wenze, Liang Chao, Duan Xuhua

机构信息

Department of Interventional Radiology, The First Affiliated Hospital, Zhengzhou University, No. 1 Jianshe Road, Zhengzhou, Henan 450052, China.

Department of General ICU, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Clin Res Hepatol Gastroenterol. 2023 Jan;47(1):102060. doi: 10.1016/j.clinre.2022.102060. Epub 2022 Dec 5.

Abstract

OBJECTIVE

Camrelizumab synergizes with apatinib or transarterial chemoembolization via tumor immunity and chemosensitivity. This study aimed to investigate the efficacy and safety of camrelizumab plus apatinib with or without drug-eluting bead transarterial chemoembolization (DEB-TACE) in unresectable hepatocellular carcinoma (HCC) patients after progression to DEB-TACE plus apatinib.

METHODS

Eighty-nine unresectable HCC patients accepted previous DEB-TACE plus apatinib therapy, then further received second-line camrelizumab plus apatinib with or without DEB-TACE treatment. Treatment responses were calculated at 3 months (M3) and 6 months (M6). Survival and treatment-related adverse events were documented.

RESULTS

Objective response rate and disease control rate were 39.3% and 80.9% at M3; meanwhile, they were 22.4% and 54.1% at M6. Furthermore, the median progression-free survival (PFS) (95% confidence interval (CI)) was 7.0 (6.2-7.8) months with a 1-year PFS rate of 18.4%; the median overall survival (OS) (95% CI) was 17.0 (15.3-18.7) months with a 1-year OS rate of 73.9%. Multivariable Cox's proportional hazards regression analysis presented that 3-4 times (vs. 0 time) of DEB-TACE, apatinib dose duration> 4 months, and camrelizumab dose duration> 5 months independently predicted longer PFS (all P<0.05); meanwhile, declined ECOG PS score, new lesions as progression pattern, 1-2 and 3-4 times (vs. 0 time) of DEB-TACE, apatinib dose duration> 4 months independently predicted prolonged OS (all P<0.05). Moreover, treatment-related adverse events mainly included grade 1-2 fever, gastrointestinal reaction, fatigue, hand-foot skin reaction, and hypertension.

CONCLUSION

After progression to DEB-TACE plus apatinib treatment, the addition of camrelizumab is effective and safe among unresectable HCC patients.

摘要

目的

卡瑞利珠单抗通过肿瘤免疫和化疗敏感性与阿帕替尼或经动脉化疗栓塞协同作用。本研究旨在探讨卡瑞利珠单抗联合阿帕替尼加或不加载药微球经动脉化疗栓塞术(DEB-TACE)在不可切除肝细胞癌(HCC)患者中进展至DEB-TACE加阿帕替尼治疗后的疗效和安全性。

方法

89例不可切除的HCC患者接受了先前的DEB-TACE加阿帕替尼治疗,然后进一步接受二线卡瑞利珠单抗联合阿帕替尼加或不加DEB-TACE治疗。在3个月(M3)和6个月(M6)时计算治疗反应。记录生存情况和治疗相关不良事件。

结果

M3时客观缓解率和疾病控制率分别为39.3%和80.9%;同时,M6时分别为22.4%和54.1%。此外,中位无进展生存期(PFS)(95%置信区间(CI))为7.0(6.2-7.8)个月,1年PFS率为18.4%;中位总生存期(OS)(95%CI)为17.0(15.3-18.7)个月,1年OS率为73.9%。多变量Cox比例风险回归分析显示,3-4次(vs.0次)DEB-TACE、阿帕替尼剂量持续时间>4个月和卡瑞利珠单抗剂量持续时间>5个月独立预测更长的PFS(均P<0.05);同时,ECOG PS评分下降、以新病灶为进展模式、1-2次和3-4次(vs.0次)DEB-TACE以及阿帕替尼剂量持续时间>4个月独立预测OS延长(均P<0.05)。此外,治疗相关不良事件主要包括1-2级发热、胃肠道反应、疲劳、手足皮肤反应和高血压。

结论

在进展至DEB-TACE加阿帕替尼治疗后,加用卡瑞利珠单抗在不可切除的HCC患者中有效且安全。

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