肝脏 ›› 2024, Vol. 29 ›› Issue (4): 395-399.

• 肝癌 • 上一篇    下一篇

卡瑞利珠单抗对不可切除肝癌DTACE术后肿瘤进展的疗效和安全性

常冬冬, 殷荣华, 张燕, 周锐   

  1. 226600 江苏省海安市人民医院肿瘤科(常冬冬,殷荣华,张燕);430030 湖北 武汉市第四医院普外科(周锐)
  • 收稿日期:2023-07-23 出版日期:2024-04-30 发布日期:2024-08-27
  • 通讯作者: 周锐,Email:chunhuihavip@163.com
  • 基金资助:
    武汉市卫生健康委员会医学科研项目(WX20B15)

An evaluation on the efficacy and safety of carrilizumab on tumor progression of unresectable hepatocellular carcinoma after DTACE surgery

CHANG Dong-dong1, YIN Rong-hua1, ZHANG Yan1, ZHOU Rui2   

  1. 1. Department of Oncology, Hai ′an People′s Hospital, Jiangsu, 226600, China;
    2. Department of General Surgery, Wuhan Fourth Hospital, Hubei 430030, China
  • Received:2023-07-23 Online:2024-04-30 Published:2024-08-27
  • Contact: ZHOU Rui, Email: chunhuihavip@163.com

摘要: 目的 探讨卡瑞利珠单抗对不可切除肝细胞癌(HCC)行载药微球肝动脉化疗栓塞(DTACE)联合索拉非尼治疗后肿瘤进展患者的疗效和安全性。方法 选择海安市人民医院和武汉市第四医院2020年1月至2021年12月收治的接受DTACE联合索拉非尼治疗的不可切除中晚期HCC患者56例,随机分为观察组和对照组。对照组采用DTACE联合索拉非尼治疗,观察组在其基础上加用卡瑞利珠单抗治疗,疗程均为无法忍受的TRAE或再次疾病进展或随访截止日。观察治疗后3个月的客观有效率(ORR)和疾病控制率(DCR),随访截止日的总生存期(OS)和无进展生存期(PFS);治疗前后肿瘤标志物和肝功能指标的变化,以及相关不良事件(TRAE)发生率。结果 治疗3个月后,观察组的转化手术率、ORR、DCR、OS和PFS为17.86%、57.14%、82.14%、(13.83±2.24)个月和(8.38±1.56)个月,高于对照组的7.14%、35.71%、60.71%、(9.75±1.79)个月和(6.36±1.27)个月,差异均有统计学意义(χ2=4.039、3.853、3.481,t=8.273、8.015,均P<0.05)。治疗3个月后,观察组的血清甲胎蛋白异质体3(AFP-L3)、α-L-岩藻糖苷酶(AFU)和肿瘤特异性生长因子(TSGF)水平为(47.19±11.84)μg/L、(34.39±5.08)U/L和(52.30±5.84)U/mL,低于对照组的(80.35±16.72)μg/L、(51.46±7.35)U/L和(63.47±6.37)U/mL,差异均有统计学意义(t=9.514,8.392,8.315,均P<0.05);血清丙氨酸氨基转移酶(ALT)、γ-谷氨酰转肽酶(γ-GT)和总胆红素(TBil)为(59.46±5.28)U/L、(61.69±5.47)U/L和(19.26±3.05)μmol/L,低于对照组的(74.08±6.04)U/L、(76.25±6.29)U/L和(24.41±3.83)μmol/L,差异均有统计学意义(t=7.416、7.395、6.735,均P<0.05)。两组的TRAE均为1~2级,组间比较差异无统计学意义(P>0.05)。结论 卡瑞利珠单抗可提高DTACE联合索拉非尼靶向治疗后肿瘤进展的HCC患者疗效,且安全可控。

关键词: 肝细胞癌, 载药微球肝动脉化疗栓塞, 肿瘤进展, 卡瑞利珠单抗, 化疗相关不良事件

Abstract: Objective To investigate the efficacy and safety of carrellizumab on tumor progression in patients with unresectable hepatocellular carcinoma (HCC) after the treatment of drug-loaded microspheres of hepatic artery chemoembolization (DTACE) and sorafenib. Methods Fifty-six advanced patients with unresectable HCC treated with DTACE in combination with sorafenib from January 2020 to December 2021 in Haian People’s Hospital and Wuhan Fourth Hospital were selected and randomly divided into an observation group and a control group. The control group continually received DTACE treatment in combination with sorafenib. The observation group was additionally treated with carrilizumab. All with intolerable TRAE, or disease re-progression, or follow-up till deadline as the course of treatment. Both groups of patients were observed and compared about their objective response rate (ORR) and disease control rate (DCR) in 3 months after treatment, their overall survival (OS) and progression-free survival (PFS) at follow-up deadline, the changes in tumor markers and liver function indicators before and after the treatments, and the incidence of chemotherapy-related adverse events (TRAE). Results In three months after treatment, the conversion operation rate, ORR, DCR, OS and PFS in the observation group were 17.86%, 57.14%, 82.14%, 13.83±2.24 months and 8.38±1.56 months, respectively, which were higher than those of 7.14%, 35.71%, 60.71%, 9.75±1.79 months and 6.36±1.27 months in the control group, with statistical significance (χ2=4.039, 3.853, 3.481, t=8.273, 8.015, all P<0.05). After 3 months of treatment, the serum levels of alpha-fetoprotein anisoplast 3 (AFP-L3), α-L-fucoidase (AFU) and tumor-specific growth factor (TSGF) in the observation group were 47.19±11.84 mg/L, 34.39±5.08 U/L and 52.30±5.84 U/mL, respectively, which were significantly lower than those of 80.35±16.72 mg/L, 51.46±7.35 U/L and 63.47±6.37 U/mL in the control group (t=9.514, 8.392, 8.315, all P<0.05). Serum alanine aminotransferase (ALT), γ-glutamyl transpeptidyase (γ-GT) and total bilirubin (TBil) were 59.46±5.28 U/L, 61.69±5.47 U/L and 19.26±3.05 μmol/L, respectively, which were significantly lower than those of 74.08±6.04 U/L, 76.25±6.29 U/L and 24.41±3.83 μmol/L in the control group (t=7.416, 7.395, 6.735, all P<0.05). The TRAE in both groups were level 1~2, and there was no significant difference between the two groups (P>0.05). Conclusion Carrilizumab can improve the efficacy of DTACE in combination with sorafenib treatment to prevent tumor progression in patients with unresectable HCC, which benefits the patients with safety and controllability.

Key words: Hepatocellular carcinoma, Drug-loaded microspheres of hepatic artery chemoembolization, Tumor microenvironment, Tumor progression, Carrellizumab, Chemotherapy-related adverse events