实用医学杂志 ›› 2022, Vol. 38 ›› Issue (9): 1130-1135.doi: 10.3969/j.issn.1006⁃5725.2022.09.016

• 药物与临床 • 上一篇    下一篇

信迪利单抗联合仑伐替尼二线治疗不可切除肝细胞肝癌的临床疗效及安全性

王俊洁1 徐龙1 袁国盛2 许晓明1 周晓元1 罗润齐1    

  1. 1 广州医科大学附属第二医院感染科(广州 510260);2 南方医科大学南方医院感染科(广州 510515)

  • 出版日期:2022-05-10 发布日期:2022-05-10
  • 基金资助:
    中国博士后基金面上项目基金资助项目(编号:2021M691468);国家自然科学基金青年项目(编号:82102879);广州市卫生局医药卫生科技项目(编号:20171A011305)

Efficacy and safety of sintilimab in combination with lenvatinib therapy as second⁃line regimen for patients with unresectable hepatocellular carcinoma

WANG Junjie*,XU Long,YUAN Guosheng,XU Xiaoming,ZHOU Xiaoyuan,LUO Runqi.   

  1. Department of Infectious Disease,the Second Affiliated Hospital,Guangzhou Medical Univer⁃ sity,Guangzhou 510260,China

  • Online:2022-05-10 Published:2022-05-10

摘要:

目的 分析信迪利单抗联合仑伐替尼二线治疗不可切除肝细胞癌(hepatocellular carcinoma HCC)的临床疗效及安全性。方法 回顾性纳入 39 例接受信迪利单抗联合仑伐替尼、36 例单用仑伐替尼 二线治疗的中晚期 HCC 患者。收集患者治疗基线的血常规、肝功能、肾功能、肿瘤分期、肿瘤影像学特 征、既往接受的治疗策略等临床资料,定期随访患者的影像学复查结果、治疗过程中出现的不良反应,直 至患者随访截止或失访或死亡。使用 mRECIST 标准评价疗效,Kaplan⁃Meier 法绘制生存曲线。结果 至末次随访,两组患者均未获得 CR。39 例患者接受信迪利单抗联合仑伐替尼治疗后,15 例(38.4%)例获 得部分缓解,14例(35.9%)获得疾病稳定,10例(25.8%)疾病进展;ORR为38.5%;DCR为74.4%。36例患者 单用仑伐替尼治疗后,6 例(16.7%)获得部分缓解,14 例(35.8%)获得疾病稳定,10 例(25.8%)疾病进展; ORR为38.5%;DCR为74.4%。联合治疗组中位PFS时间为9.1个月(95%CI:7.5 ~ 10.7),仑伐替尼单药组中 PFS 时间为 5.9 个月(95%CI:4.7 ~ 7.1);两组间 PFS 比较差异有统计学意义(P < 0.001)。联合治疗组中 OS 时间为 18.4 个月(95%CI:16.5 ~ 20.3),仑伐替尼单药组中位 OS 时间为 11.6 个月(95%CI:7.2 ~ 16.0); 两组间 OS 比较差异有统计学意义(P = 0.016)。3 级以上不良事件主要有高血压、腹泻,不良反应均得到 有效控制。结论 信迪利单抗联合仑伐替尼治疗可有效延长中晚期肝癌患者的生存期,严重不良反应发 生率低,是一种安全、有效的治疗方案。

关键词: 肝细胞癌, 信迪利单抗, 仑伐替尼, 安全性, 临床疗效

Abstract:

Objective To analysis the efficacy and tolerability of sintilimab in combination with lenvatinib therapy as second ⁃line regimen for patients with hepatocellular carcinoma(HCC). Methods We retrospectively analyzed the data of 39 patients with unresectable HCC treated with sintilimab in combination with lenvatinib as second⁃line therapy,as well as the data of another 36 patients treated with lenvatinib therapy as contrast. The clinical data such as the baseline data from blood routine test liver function test,renal function test tumor staging,tumor imaging features,previous treatment strategies,follow ⁃ up imaging results and adverse events during follow ⁃ ups were recorded. The Modified Response Evaluation Criteria in Solid Tumors was used to evaluate the treatment out⁃ come of intrahepatic lesions and the Kaplan⁃Meier method was used to evaluate survival time. Results All through the follow⁃ups,the treatments for the patients from both groups did not reached complete response. Among the 39 patients treated with sintilimab plus lenvatinib,15 cases achieved partial remission(PR),accounting for 38.4% 14 disease stability(DS),accounting for 35.9% ,and 10 progressive disease,accounting for 25.8%,with the ORR and DCR of 38.5% and 74.4%,respectively. Among the 36 patients in the control group,6 cases achieved partial remission,accounting for 16.7%,14 disease stability,accounting for 35.8%,and 10 progressive disease,accounting for 25.8%,with the ORR and DCR of 38.5% and 74.4%,respectively. The median progression⁃free survival(PFS was 9.1 months in the combination group(95%CI:7.5 ~ 10.7)and 5.9 months(95%CI:4.7 ~ 7.1)in the control group,with a statistically significant difference between the two groups(P < 0.001). Median Overall Survival(OS time in the combination group was 18.4 months(95%CI:16.5 ~ 20.3)and 11.6 months(95%CI:7.2 ~ 16.0)in the control group,with a statistical difference between the two groups(P = 0.016). Grade ≥ 3 treatment ⁃related ad⁃ verse events (TRAEs included hypertension and diarrhea. All TRAEs were effectively controlled. Conclu⁃ sion Sintilimab combined with lenvatinibcan yield a promising outcome in treating the patients with unresectable HCC for its low incidence rate of serious adverse eventsand thus it is a safe and effective treatment regimen.

Key words:

hepatocellular carcinoma, sintilimab, lenvatinib, safety, efficacy