肝脏 ›› 2023, Vol. 28 ›› Issue (12): 1440-1445.

• 肝癌 • 上一篇    下一篇

卡瑞利珠单抗联合仑伐替尼或阿帕替尼对晚期肝癌患者肝功能及肿瘤标志物的影响

曹静, 夏晓阳, 尤冬山, 黄景慧, 周芸娜   

  1. 239000 安徽医科大学附属滁州医院(滁州市第一人民医院)肿瘤内三科
  • 收稿日期:2023-04-21 出版日期:2023-12-31 发布日期:2024-03-01
  • 通讯作者: 夏晓阳

Influence of camrelizumab combined with lenvatinib or apatinib on liver function and tumor markers in patients with advanced hepatocarcinoma

CAO Jing, XIA Xiao-yang, YOU Dong-shan, HUANG Jing-hui, ZHOU Yun-na   

  1. The Third Department of Oncology, the First People's Hospital of Chuzhou, Anhui 239000, China
  • Received:2023-04-21 Online:2023-12-31 Published:2024-03-01
  • Contact: XIA Xiao-yang

摘要: 目的 研究卡瑞利珠单抗联合仑伐替尼或阿帕替尼治疗晚期肝癌的疗效及对肝功能、肿瘤标志物的影响。方法 收集2019年12月—2021年10月期间安徽医科大学附属滁州医院收治的晚期肝癌患者96例,根据治疗方案分为两组:48例使用卡瑞利珠单抗联合仑伐替尼治疗为观察组,48例使用卡瑞利珠单抗联合阿帕替尼治疗为对照组。比较两组近期疗效,治疗前及治疗后检测总胆红素(TBil)、天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、甲胎蛋白(AFP)、癌胚抗原(CEA)、糖类抗原199(CA199)和α-L-岩藻糖苷酶(AFU)水平,随访患者的生存情况。结果 治疗后,观察组的TBil、AST、ALT分别为(20.12±2.03)μmol/L、(43.58±4.12)U/L、(43.46±4.82)U/L,较对照组的(22.06±3.19)μmol/L、(47.62±5.28)U/L、(46.55±6.13)U/L降幅更明显(P<0.05)。治疗后,观察组的AFP、CEA、CA199、AFU分别为(101.45±16.22)μg/L、(16.83±3.62)ng/mL、(143.21±21.65)U/mL、(35.02±5.69)U/L,较对照组的(124.87±21.69)μg/L、(18.75±4.43)ng/mL、(166.21±35.16)U/mL、(38.36±7.84)U/L明显降低(P<0.05)。观察组客观缓解率(ORR)和疾病控制率(DCR)分别为50.00%、83.33%,高于对照组的33.33%、68.75%(P<0.05)。观察组中位无进展生存期(PFS)为9.6个月,较对照组的6.2个月明显延长(P<0.05)。两组毒副反应发生类型及发生率差异不显著,均无因严重毒副作用而停药或退出研究者。结论 卡瑞利珠单抗联合仑伐替尼或阿帕替尼治疗晚期肝癌均可在一定程度上保护肝功能和下调肿瘤标志物水平,毒副反应相对可控,而患者从卡瑞利珠单抗联合仑伐替尼中的生存获益可能优于联合阿帕替尼。

关键词: 晚期肝癌, 卡瑞利珠单抗, 仑伐替尼, 阿帕替尼, 肝功能, 肿瘤标志物

Abstract: Objective To investigate the efficacy of carlizumab combined with lenvatinib or apatinib in the treatment of advanced hepatocarcinoma and its influence on liver function and tumor markers.Methods A total of 96 patients with advanced hepatocarcinoma admitted to the First People's Hospital of Chuzhou between December 2019 and October 2021 were divided into two groups based on their treatment plan. The observation group consisted of 48 patients treated with camrelizumab combined with lenvatinib, while the control group consisted of 48 patients treated with camrelizumab combined with apatinib. The short-term efficacy of the two groups was compared by examining the serum leves of total bilirubin (TBil), aspartate aminotransferase (AST), alanine aminotransferase (ALT), alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), carbohydrate antigen 199 (CA199) and α- L-fucosidase (AFU). Furthermore, patient survival was followed up for assessment.Results After treatment, the serum levels of TBil, AST, ALT in the observation group were (20.12±2.03) μmol/L, (43.58±4.12) U/L and (43.46±4.82) U/L, respectively. These levels were significantly lower than those in the control group [(22.06±3.19) μmol/L, (47.62±5.28) U/L, (46.55±6.13) U/L, (P<0.05)]. After treatment, the serum levels of AFP, CEA, CA199 and AFU in the observation group were (101.45±16.22) μg/L, (16.83±3.62) ng/mL, (143.21±21.65) U/mL, (35.02±5.69) U/L, respectively. These levels were significantly lower than those in the control group [(124.87±21.69) μg/L, (18.75±4.43) ng/mL, (166.21±35.16) U/mL, (38.36±7.84) U/L,(P<0.05)]. Additionally, the Objective response rate (ORR) and disease control rate (DCR) of group A were 50.00% and 83.33%, respectively, both of which were higher than those in the control group (33.33% and 68.75%, P<0.05). Furthermore, the median progression-free survival (PFS) in the observation group was 9.6 months, which was significantly longer than 6.2 months in the control group (P<0.05). There were no significant differences in the type and incidence of toxic and side effects between the two groups, and there were no drug withdrawal or drop-outs due to serious treatment-emergent adverse events.Conclusion The combination of camrelizumab with lenvatinib or apatinib in the treatment of advanced hepatocarcinoma has demonstrated promising results in protecting liver function and reducing the level of tumor markers. The toxicity and side effects of this treatment approach are relatively manageable. However, patients may benefit more in terms of survival from the combination of camrelizumab and lenvatinib than from the combination of camrelizumab and apatinib.

Key words: Advanced hepatocarcinoma, Camrelizumab, Lenvatinib, Apatinib, Liver function, Tumor markers