Zhou Yuanlong, Wang Yuan, Zhao Jisen, Kang Linwei, Li Zan
Yuanlong Zhou, Department of Hepatobiliary Surgery, Affiliated Hospital of Hebei University, Baoding 071000, Hebei, China.
Yuan Wang. Department of Hepatobiliary Surgery, Affiliated Hospital of Hebei University, Baoding 071000, Hebei, China.
Pak J Med Sci. 2025 Mar;41(3):821-826. doi: 10.12669/pjms.41.3.9799.
To investigate the clinical efficacy and safety of transarterial chemoembolization(TACE) combined with targeted therapy and PD1 inhibitors in patients with advanced liver cancer.
This was a retrospective study. A total of 120 patients with advanced primary liver cancer admitted to Affiliated Hospital of Hebei University were randomly divided into two groups, with 60 patients in each group from May 2020 to May 2023. Patients in the control group received conventional TACE, and those in the experimental group received 200 mg camrelizumab once every 21 days and oral lenvatinib mesylate capsules once daily in addition to TACE. Compared the clinical efficacy, levels of tumor markers, T lymphocyte subsets, and adverse drug reactions after treatment and the improvement of quality of life(QOL) before and after treatment between the two groups of patients.
The overall response rate(ORR) was 80% in the experimental group and 62% in the control group, and the difference was statistically significant(p=0.03); the incidence of adverse reactions was 28% in the experimental group and 25% in the control group, with no significant difference between the two groups(p=0.68); the improvement rate of QOL score was significantly increased(p=0.03) and the deterioration rate was significantly decreased(p=0.01) in the experimental group compared with those in the control group, respectively.
TACE combined with targeted therapy and PD1 inhibitors is significantly effective to improve the cellular immune function with no significant increase in the incidence of adverse reactions, making it an effective and safe treatment option for patients with liver cancer.
探讨经动脉化疗栓塞术(TACE)联合靶向治疗及PD1抑制剂治疗晚期肝癌患者的临床疗效及安全性。
本研究为回顾性研究。选取2020年5月至2023年5月在河北大学附属医院收治的120例晚期原发性肝癌患者,随机分为两组,每组60例。对照组患者接受常规TACE治疗,试验组患者在TACE基础上,每21天接受一次200mg卡瑞利珠单抗治疗,同时每日口服甲磺酸仑伐替尼胶囊。比较两组患者治疗后的临床疗效、肿瘤标志物水平、T淋巴细胞亚群及药物不良反应,以及治疗前后生活质量(QOL)的改善情况。
试验组的总缓解率(ORR)为80%,对照组为62%,差异有统计学意义(p=0.03);试验组不良反应发生率为28%,对照组为25%,两组间差异无统计学意义(p=0.68);试验组QOL评分改善率显著升高(p=0.03),恶化率显著降低(p=0.01)。
TACE联合靶向治疗及PD1抑制剂可显著提高细胞免疫功能,且不良反应发生率无显著增加,是肝癌患者有效且安全的治疗选择。