首页|经肝动脉化疗栓塞联合酪氨酸激酶抑制剂及程序性死亡受体-1抗体治疗中晚期不可切除肝细胞癌的临床疗效和安全性分析

经肝动脉化疗栓塞联合酪氨酸激酶抑制剂及程序性死亡受体-1抗体治疗中晚期不可切除肝细胞癌的临床疗效和安全性分析

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目的 探讨经肝动脉化疗栓塞术(TACE)联合酪氨酸激酶抑制剂(TKIs)及程序性死亡受体-1(PD-1)抑制剂治疗中晚期不可切除肝细胞癌(以下简称肝癌)的临床效果.方法 2020年1月~2022年1月我院收治的中晚期不可切除肝癌病人65例,均采用TACE+TKIs+PD-1抗体治疗.观察肿瘤反应、客观缓解率、疾病控制率、总生存时间、无进展生存时间、转化手术率和药物不良反应等.结果 65例病人的客观缓解率为49.2%(32/65),疾病控制率为89.2%(58/65),其中完全缓解2例,部分缓解30例,疾病稳定26例,疾病进展7例.65例病人中,18例转化为可切除肝癌,行R0手术切除,转化手术率为27.6%(18/65).65例病人均获得随访,随访时间3~22.4个月,中位随访时间16.5个月.65例病人中位总体生存时间、中位疾病无进展生存时间分别为14.5个月(95%CI为12.3~16.6个月)、8.8个月(95%CI为6.9~10.6个月).65例病人治疗后均出现栓塞后综合征(腹痛、发热、恶心、呕吐等症状),部分病人出现短暂的肝功能异常.3级以下药物不良反应均在1周内恢复.部分病人合并多种药物不良反应.其中1例(1.5%)因顽固性呕吐停用TACE治疗,5例因治疗过程中严重肝功能损伤停用仑伐替尼,2例因严重反应性毛细血管增生停用卡瑞利珠单抗,1例因严重甲状腺功能减退停用替雷利珠单抗,1例因顽固消化道出血停用仑伐替尼及信迪利单抗.其他治疗病人发生3~4级药物不良反应经药物减量及对症处理后均缓解.结论 TACE+TKIs+PD-1抗体治疗中晚期不可切除肝癌可靠、安全.
Efficacy and safety of transhepatic arterial chemoembolization combined with tyrosine kinase inhibitor and programmed death receptor-1 inhibitors in the treatment of intermediate and a-dvanced unresectable hepatocellular carcinoma
Objective To investigate the clinical effect of transhepatic arterial chemoembolization(TACE)combined with tyrosine kinase inhibitors(TKIs)and programmed death receptors-1(PD-1)inhibitors(TACE+TKIs+PD-1 antibody)in the treatment of moderate advanced unresectable hepatocellular carcinoma(HCC).Methods The clinical data of 65 patients with moderate advanced unresectable hepatocellular carcinoma admitted to the Affiliated Hospital of North Sichuan Medical College from January 2020 to January 2022 were analyzed retrospectively.65 patients were treated with TACE+TKIs+PD-1 antibody.The observation indexes were tumor response,objective response rate(ORR),disease control rate(DCR),total survival time,progression free survival time,conversion operation rate and adverse drug reaction.Results The ORR of 65 p-atients with hepatocellular carcinoma was 49.2%(32/65),and the DCR was 89.2%(58/65).Among them,there were 2 patients with complete remission(CR),30 patients with partial remission(PR),26 patients with stable disease(SD),and 7 patients with progression disease(PD).Among 65 patients with hepatocellular carcinoma,18 patients were transformed into resectable hepatocell-ular carcinoma and underwent RO surgery.The conversion rate was 27.6%(18/65).65 patients were followed up for 3 to 22.4 months,The median follow-up time was 16.5 months.The median overall survival time and median disease progression free survival time of 65 patients were 14.5 months(95%CI:12.3~16.6 months)and 8.8 months(95%CI:6.9~10.6 months),respectively.After treatment,65 patients all had post embolism syndrome(abdominal pain,fever,nausea,vomiting and other symptoms),and some patients had transient abnormal liver function.Adverse drug reactions below grade 3 recovered within a few days.Some patients were associated with multiple adverse drug reactions.1 patient(1.5%)stopped using TACE because of stubborn vomiting,and 5 patients(7.6%)stopped using Lenvatinib because of severe liver function damage during treatment,2 patients(3%)stopped using Camrelizumab because of severe reactive capillary hyperplasia,one patient(1.5%)stopped using Tislelizumab because of severe hypothyroidism,one patient(1.5%)stopped the treatment of Lenvatinib and Sintilimab due to severe gastrointestinal bleeding.The adverse drug reactions of grade 3~4 occurred in other patients were alleviated after drug reduction,symptomatic treatment and hormone treatment.Conclusion TACE+TKIs+PD-1 antibody can obtain reliable clinical efficacy and anti-tumor activity in the treatment of moderate advanced unresectable hepatocellular carcinoma.

hepatocellular carcinomatranscatheter arterial chemoembolizationtyrosine kinase inhibitorprogrammed death receptor-1 inhibitorclinical efficacy

熊坚威、李强、唐涛、张立鑫、英保、赵开烽、熊永福、李敬东、武国

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637000 四川南充,川北医学院附属医院肝胆外一科,川北医学院肝胆胰肠疾病研究所

肝细胞癌 经动脉化疗栓塞 酪氨酸激酶抑制剂 程序性死亡受体-1抑制剂 临床疗效

2024

临床外科杂志
中华医学会湖北分会

临床外科杂志

CSTPCD
影响因子:0.716
ISSN:1005-6483
年,卷(期):2024.32(2)
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