实用肝脏病杂志 ›› 2026, Vol. 29 ›› Issue (3): 401-404.doi: 10.3969/j.issn.1672-5069.2026.03.021

• 肝癌 • 上一篇    下一篇

甲磺酸仑伐替尼联合特瑞普利单抗治疗晚期原发性肝癌患者效果研究*

蔡蓓蓓, 韦海燕, 顾丽英   

  1. 223800 江苏省宿迁市 徐州医科大学附属宿迁医院/南京鼓楼医院集团宿迁医院肿瘤科
  • 收稿日期:2025-12-16 出版日期:2026-05-10 发布日期:2026-05-18
  • 通讯作者: 顾丽英,E-mail:13739130270@163.com
  • 作者简介:蔡蓓蓓,女,39岁,大学本科,主治医师。E-mail:18012183655@163.com
  • 基金资助:
    *江苏省卫生健康委科研项目(编号:Z2021062)

Lenvatinib mesylate and toripalimab combination in the treatment of patients with advanced primary liver cancer

Cai Beibei, Wei Haiyan, Gu Liying   

  1. Department of Oncology, Suqian Hospital, Nanjing Drum Tower Hospital Group Affiliated to Xuzhou Medical University, Suqian 223800, Jiangsu Province, China
  • Received:2025-12-16 Online:2026-05-10 Published:2026-05-18

摘要: 目的 探讨甲磺酸仑伐替尼联合特瑞普利单抗治疗晚期原发性肝癌(PLC)患者的效果。方法 2021年8月~2024年8月我院收治的102例不能手术切除的PLC患者被随机分为两组,每组51例,给予对照组甲磺酸仑伐替尼治疗,给予观察组甲磺酸仑伐替尼联合特瑞普利单抗治疗,两组均治疗3个周期。采用化学发光免疫法检测血清肿瘤特异性生长因子(TSGF)、甲胎蛋白(AFP)和异常凝血酶原-Ⅱ(PIVKA-Ⅱ),使用流式细胞仪检测外周血淋巴细胞亚群。结果 治疗后,观察组客观缓解率和疾病控制率分别为58.8%和82.4%,均显著高于对照组的37.3%和62.8%(P<0.05);观察组血清TSGF、AFP和PIVKA-Ⅱ水平分别为(60.3±6.5)U/mL、(142.9±19.1)μg/L和(871.8±91.4)ng/mL,均显著低于对照组【分别为(70.2±7.3)U/mL、(227.1±31.8)μg/L和(1029.7±95.3)ng/mL,P<0.05】;观察组外周血CD3+和CD4+细胞百分比及CD4+/CD8+细胞比值分别为(42.3±5.4)%、(33.4±3.9)%和(1.4±0.4),均显著高于对照组【分别为(39.5±4.8)%、(29.3±3.5)%和(1.1±0.3),P<0.05】,而CD8+细胞百分比为(23.2±3.1)%,显著低于对照组【(26.3±3.7)%,P<0.05】。结论 应用甲磺酸仑伐替尼联合特瑞普利单抗治疗晚期PLC患者具有一定的短期疗效,可能与抑制了肿瘤生长和增强了机体免疫功能有关。

关键词: 原发性肝癌, 不可切除, 甲磺酸仑伐替尼, 特瑞普利单抗, 淋巴细胞亚群, 治疗

Abstract: Objective The aim of this study was to investigate clinical efficacy of lenvatinib mesylate in combination with toripalimab in the treatment of patients with advanced primary liver cancer(aPLC). Methods 102 patients with aPLC were encountered in our hospital between August 2021 and August 2024, and were randomly divided into control and observation group, with 51 cases in each group. Patients in the control group were treated with lenvatinib mesylate alone, while those in the observation group received lenvatinib mesylate and toripalimab combination therapy. Anti-tumor regimen lasted for three cycles (21 days one cycle) in the two groups. Serum tumor-specific growth factor (TSGF), alpha-fetoprotein (AFP) and abnormal prothrombin-Ⅱ (PIVKA-Ⅱ) levels were detected by chemiluminescence immunoassay. Peripheral blood T lymphocyte subsets were determined by flow cytometry. Results Objective remission rate and disease control rate in the observation group were 58.8% and 82.4%, both much higher than 37.3% and 62.8%(P<0.05) in the control group; serum TSGF, AFP and PIVKA-Ⅱ levels were (60.3±6.5)U/mL, (142.9±19.1)μg/L and (871.8±91.4)ng/mL, all significantly lower than [(70.2±7.3)U/mL, (227.1±31.8)μg/L and (1029.7±95.3)ng/mL, respectively, P<0.05] in the control; percentages of peripheral blood CD3+ and CD4+ cells, and CD4+/CD8+ cell ratio were (42.3±5.4)%, (33.4±3.9)% and (1.4±0.4), all much higher than [(39.5±4.8)%, (29.3±3.5)% and (1.1±0.3), respectively, P<0.05], while percentage of CD8+ cells was (23.2±3.1)%, much lower than [(26.3±3.7)%, P<0.05] in the control group. Conclusion Lenvatinib mesylate in combination with toripalimab therapy exhibits a short-term promising efficacy in the treatment of patients with aPLC, which might be owning to improvement of body immune functions and inhibition of tumor growth.

Key words: Hepatoma, Advanced, Lenvatinib mesylate, Toripalimab, Lymphocyte subsets, Therapy