Department of Radiology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan; Department of Electrical Engineering, National Taipei University of Technology, Taipei, Taiwan.
Division of Gastroenterology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Eur J Radiol. 2024 Jan;170:111266. doi: 10.1016/j.ejrad.2023.111266. Epub 2023 Dec 15.
To analyze the safety of combination treatment comprising drug-eluting bead transarterial chemoembolization (DEB-TACE) and immune checkpoint inhibitors (ICIs) in hepatocellular carcinoma (HCC).
In total, 208 HCC patients receiving DEB-TACE were enrolled for this retrospective single-institution study. Among them, 50 patients who received ICIs at an interval less than one month from DEB-TACE were categorized into the DEB-ICI group; the remaining 158 patients were categorized into the DEB group. Albumin-bilirubin (ALBI) score before and at three months after DEB-TACE were recorded to evaluate liver function changes. Adverse events within three months after DEB-TACE were considered TACE-related and were compared between the two groups.
The DEB-ICI group had significantly higher incidence of liver abscess than the DEB group (14.0 % versus 5.1 %, p-value = 0.0337). No significant difference in the other TACE-related adverse events and change of ALBI score between the groups. Univariate logistic regression confirmed that combination with ICIs was an independent risk factor for liver abscess after DEB-TACE (odds ratio = 3.0523, 95 % confidence interval: 1.0474-8.8947, p-value = 0.0409); other parameters including subjective angiographic chemoembolization endpoint scale and combined targeted therapy were nonsignificant risk factors in this study population. In the DEB-ICI group, patients who received ICIs before DEB-TACE exhibited a trend toward liver abscess formation compared with those who received DEB-TACE before ICIs (23.8 % versus 6.9 %, p-value = 0.0922).
Combination treatment involving DEB-TACE and ICIs at an interval less than one month increased the risk of liver abscess after DEB-TACE. Greater caution is therefore warranted for HCC patients who receive ICIs and DEB-TACE with this short interval.
分析载药微球动脉化疗栓塞术(DEB-TACE)联合免疫检查点抑制剂(ICI)治疗肝细胞癌(HCC)的安全性。
本回顾性单中心研究共纳入 208 例接受 DEB-TACE 治疗的 HCC 患者。其中,50 例患者在 DEB-TACE 后 1 个月内接受 ICI 治疗,归入 DEB-ICI 组;其余 158 例归入 DEB 组。记录 DEB-TACE 前后 3 个月的白蛋白-胆红素(ALBI)评分,以评估肝功能变化。比较两组患者 DEB-TACE 后 3 个月内的不良事件。
DEB-ICI 组肝脓肿的发生率明显高于 DEB 组(14.0%比 5.1%,p 值=0.0337)。两组间其他 TACE 相关不良事件和 ALBI 评分变化无显著差异。单因素 logistic 回归分析证实,DEB-TACE 后联合使用 ICI 是肝脓肿的独立危险因素(比值比=3.0523,95%置信区间:1.0474-8.8947,p 值=0.0409);在该研究人群中,主观血管造影栓塞终点评分和联合靶向治疗等其他参数不是危险因素。在 DEB-ICI 组中,与先接受 DEB-TACE 后接受 ICI 的患者相比,先接受 ICI 后接受 DEB-TACE 的患者肝脓肿形成的趋势更为明显(23.8%比 6.9%,p 值=0.0922)。
DEB-TACE 联合 ICI 治疗间隔小于 1 个月会增加 DEB-TACE 后发生肝脓肿的风险。因此,对于接受 ICI 和 DEB-TACE 治疗且间隔较短的 HCC 患者,应更加谨慎。