Use of doxorubicin-eluting bead transarterial chemoembolization for unresectable hepatocellular carcinoma with portal vein invasion: a prospective study.

Su Jong Yu, Yun Bin Lee, Eun Ju Cho, Jeong-Hoon Lee, Hyo-Cheol Kim, Jin Wook Chung, Jung-Hwan Yoon, Yoon Jun Kim
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Abstract

Background/aim: To evaluate the applicability of transarterial chemoembolization (TACE) treatment with doxorubicin drug-eluting beads (DEBs) in advanced hepatocellular carcinoma (HCC) patients with portal vein invasion (PVI).

Methods: This prospective study was approved by the institutional review board and informed consent was obtained from all participants. A total of 30 HCC patients with PVI received DEB-TACE between 2015 and 2018. The following parameters were evaluated: complications during DEB-TACE, abdominal pain, fever, and laboratory outcomes, including liver function change. Overall survival (OS), time to progression (TTP), and adverse events were also analyzed and assessed.

Results: DEBs measuring 100-300 μm in diameter were loaded with doxorubicin (150 mg per procedure). There were no complications during DEB-TACE and no significant differences in the levels of prothrombin time, serum albumin, or total bilirubin at follow-up compared to baseline. The median TTP was 102 days (95% confidence interval [CI], 42-207 days) and the median OS was 216 days (95% CI, 160-336 days). Three patients (10%) had severe adverse reactions, including transient acute cholangitis (n=1), cerebellar infarction (n=1), and pulmonary embolism (n=1), but no treatment-related death occurred.

Conclusions: DEB-TACE may be a therapeutic option for advanced HCC patients with PVI.

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应用阿霉素洗脱的经动脉化疗栓塞治疗不可切除的肝细胞癌伴门静脉侵犯:一项前瞻性研究。
背景/目的:评价多柔比星药物洗脱珠(DEBs)经动脉化疗栓塞(TACE)治疗晚期肝细胞癌门静脉侵犯(PVI)的适用性。方法:本前瞻性研究经机构审查委员会批准,并获得所有参与者的知情同意。2015年至2018年间,共有30例肝癌合并PVI患者接受了DEB-TACE治疗。评估以下参数:DEB-TACE期间的并发症、腹痛、发热和实验室结果,包括肝功能改变。总生存期(OS)、进展时间(TTP)和不良事件也进行了分析和评估。结果:直径100-300 μm的deb被加载阿霉素(150 mg /次)。DEB-TACE期间无并发症,随访时凝血酶原时间、血清白蛋白或总胆红素水平与基线相比无显著差异。中位TTP为102天(95%置信区间[CI], 42-207天),中位OS为216天(95% CI, 160-336天)。3例(10%)患者出现严重不良反应,包括短暂性急性胆管炎(n=1)、小脑梗死(n=1)和肺栓塞(n=1),但未发生治疗相关死亡。结论:DEB-TACE可能是晚期肝癌合并PVI患者的一种治疗选择。
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