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Safety and efficacy of DEM-TACE performed with drug-eluting microspheres smaller than 300μm in patients with HCC and TIPS
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作者 Pierleone Lucatelli Simone Zilahi De Gyurgyokai +12 位作者 Gianluca De Rubeis Renato Argirò Simone Ciaglia Bianca Rocco Flaminia Ferri Simona Parisse Mariana Forlino Alessandro Cannavale FabrizioBasilico Pier Giorgio Nardis Mario Corona Vito Cantisani Carlo Catalano 《Hepatoma Research》 2022年第1期193-206,共14页
Aim:Safety and efficacy evidence of drug-eluting-microspheres trans-arterial chemoembolization(DEM-TACE)in patients with hepatocellular carcinoma(HCC)and trans-jugular intrahepatic portosystemic shunt(TIPS)is lacking.... Aim:Safety and efficacy evidence of drug-eluting-microspheres trans-arterial chemoembolization(DEM-TACE)in patients with hepatocellular carcinoma(HCC)and trans-jugular intrahepatic portosystemic shunt(TIPS)is lacking.The aim of this retrospective study was to report the safety and efficacy of DEM-TACE procedures performed with microspheres smaller than 300μm in patients with HCC and TIPS in a high-volume transplant center.Methods:Embolization was standardized by initiating DEM-TACE with microspheres smaller than 100μm,and if stasis was not achieved,adjunctive embolization with 100-300 or 200μm microspheres was administered.With regards to efficacy,the oncological response was evaluated and categorized according to mRECIST criteria at 1,3-6,9-12,and 15-18 months.Reporting the safety profile,detailed laboratory analysis was performed before,at 36-48 h,and 30-60 days after the procedure.Adverse events(AEs)were recorded;post-embolic syndrome was defined as the onset of fever/nausea/pain after the procedure.Late onset hepatobiliary complications were evaluated by follow-up imaging with computed tomography or magnetic resonance(CT/MR).Results:From December 2007 to November 2020,17 HCC patients(25 HCC nodules)with patent TIPS underwent 20 DEM-TACE.Embolization was performed only with microspheres smaller than 100μm in 3/20 DEM-TACE(15%);adjunctive embolization with 100-300 or 200μm microspheres was required in 17/20 DEMTACE(85%).Reported early AEs were post-embolic syndrome(9/20;45%)all of grade 1-2,late AEs were asymptomatic acute liver bile duct injury(2/20;10%),and in one case we observed hepatic abscess(1/20;5%)resulting in death due to sepsis.With regards to efficacy,the oncological response was evaluated and categorized according to mRECIST criteria.Complete response(CR)at 1,3-6,9-12,and 15-18 months was 52%,50%,50%,and 50%,respectively.Objective response(CR+partial response)at 1,3-6,9-12,and 15-18 months was 95%,71%,70%,and 50%,respectively.Conclusion:DEM-TACE with drug-eluting-microspheres smaller than 300μm can be performed in appropriately selected patients with TIPS. 展开更多
关键词 HCC TIPS dem-tace CT MR
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信迪利单抗及贝伐珠单抗联合载药微球在中晚期肝癌患者中的临床应用
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作者 孙丽霞 徐琍 +1 位作者 丁晓燕 王庆莲 《实用药物与临床》 2026年第1期31-36,共6页
目的探讨信迪利单抗^(+)贝伐珠单抗联合载药微球经肝动脉化疗栓塞术(DEM-TACE)治疗中晚期肝癌的临床疗效及安全性。方法采用回顾性队列研究,收集2023年3月至2024年3月首都医科大学附属北京地坛医院收治的89例中晚期肝癌患者相关临床资... 目的探讨信迪利单抗^(+)贝伐珠单抗联合载药微球经肝动脉化疗栓塞术(DEM-TACE)治疗中晚期肝癌的临床疗效及安全性。方法采用回顾性队列研究,收集2023年3月至2024年3月首都医科大学附属北京地坛医院收治的89例中晚期肝癌患者相关临床资料。所有患者均接受信迪利单抗^(+)贝伐珠单抗治疗,根据肝动脉化疗栓塞术的不同,分为DEM-TACE组(n=45)和传统经肝动脉化疗栓塞术(cTACE)组(n=44)。评估两组患者治疗3个月后的临床疗效,包括肿瘤应答[客观缓解率(ORR)、疾病控制率(DCR)]、肿瘤标志物[癌胚抗原(CEA)、甲胎蛋白(AFP)、糖类抗原19-9(CA19-9)]、免疫指标[CD3^(+)T淋巴细胞(%)、CD4^(+)T淋巴细胞(%)、CD8^(+)T淋巴细胞(%)、CD4^(+)/CD8^(+)T淋巴细胞比值]、血管内皮生长因子(VEGF),记录无进展生存期(PFS)、总生存期(OS)及安全性。结果两组患者基线资料(如年龄、性别、疾病分期等)比较,差异无统计学意义(P>0.05)。治疗3个月后,DEM-TACE组ORR高于cTACE组(80.00%vs.59.10%,P<0.05),CEA、AFP、CA19-9、VEGF水平低于cTACE组(P<0.05),CD3^(+)T淋巴细胞(%)、CD4^(+)T淋巴细胞(%)、CD8^(+)T淋巴细胞(%)、CD4^(+)/CD8^(+)T淋巴细胞比值高于cTACE组(P<0.05)。随访截止时,DEM-TACE组中位PFS显著高于cTACE组(17.3个月vs.11.8个月,P<0.05)。两组不良反应发生率比较,差异无统计学意义(28.89%vs.20.45%,P>0.05)。结论信迪利单抗^(+)贝伐珠单抗联合DEM-TACE可显著提升抗肿瘤应答,抑制血管生成,延长无进展生存期,且安全性良好。 展开更多
关键词 肝癌 载药微球经皮肝动脉化疗栓塞术(dem-tace) 传统经皮肝动脉化疗栓塞术(cTACE) 信迪利单抗 贝伐珠单抗
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