Department of Diagnostic Radiology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taiwan.
Diagn Interv Radiol. 2020 May;26(3):230-235. doi: 10.5152/dir.2019.19261.
We aimed to compare the safety and effectiveness of 100-300 μm versus 300-500 μm drug-eluting bead transarterial chemoembolization (DEB-TACE) and to investigate the impact of tumor and feeding artery size on treatment outcome of different particle sizes in the treatment of hepatocellular carcinoma (HCC).
This retrospective cohort study enrolled 234 consecutive patients who underwent TACE using 100-300 μm DEB (Group A, n=75) and 300-500 μm DEB (Group B, n=159) in a tertiary center between August 2012 and March 2017. Initial treatment response and adverse events were assessed using modified Response Evaluation Criteria in Solid Tumors (mRECIST) and National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, respectively.
A total of 704 HCCs in 234 patients were evaluated. The average index tumor size was 3.8 cm. Multivariate analysis showed that tumor size, lobe involvement, particle size, and tumor location were significant predictive factors of complete response. The overall rate of complete response in groups A and B were 56.0% and 33.3% (P = 0.001), respectively. Group A had higher complete response rate than group B in the subgroup of BCLC B with tumor <3 cm (57.9% vs. 21.1%; P = 0.020) and subgroup of feeding artery ≥0.9 mm (55.2% vs. 30.9%; P = 0.014). There were fewer major complications in group A compared with group B (0% vs. 6.9%, P = 0.018).
TACE with 100-300 μm DEB is associated with better initial treatment response and fewer major complications compared with 300-500 μm. Our study also highlights the impact of tumor characteristics on treatment outcome of different DEB size, which might help to select the optimal sphere size for TACE in the treatment of HCC.
本研究旨在比较 100-300μm 与 300-500μm 载药微球经导管动脉化疗栓塞术(DEB-TACE)的安全性和有效性,并探讨肿瘤和供血动脉大小对不同粒径微球治疗肝细胞癌(HCC)疗效的影响。
本回顾性队列研究纳入 2012 年 8 月至 2017 年 3 月在一家三级中心接受 TACE 治疗的 234 例连续 HCC 患者,其中使用 100-300μm DEB(A 组,n=75)和 300-500μm DEB(B 组,n=159)。采用改良实体瘤疗效评价标准(mRECIST)和美国国立癌症研究所不良事件通用术语标准(CTCAE)第 5.0 版评估初始治疗反应和不良事件。
共评估了 234 例患者的 704 个 HCC,平均肿瘤直径为 3.8cm。多因素分析显示,肿瘤大小、肝叶受累、微球粒径和肿瘤位置是完全缓解的显著预测因素。A 组和 B 组的完全缓解率分别为 56.0%和 33.3%(P=0.001)。在肿瘤直径<3cm 的 BCLC B 期(57.9% vs. 21.1%,P=0.020)和供血动脉≥0.9mm 的亚组(55.2% vs. 30.9%,P=0.014)中,A 组的完全缓解率高于 B 组。与 B 组相比,A 组的主要并发症发生率较低(0% vs. 6.9%,P=0.018)。
与 300-500μm 载药微球相比,100-300μm 载药微球 TACE 治疗 HCC 的初始治疗反应更好,主要并发症更少。本研究还强调了肿瘤特征对不同 DEB 粒径治疗效果的影响,这可能有助于在 HCC 的 TACE 治疗中选择最佳的球径。