Department of Radiology and Research Institute of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 138-736, Korea.
Br J Radiol. 2024 May 7;97(1157):1038-1043. doi: 10.1093/bjr/tqae052.
To evaluate the safety and effectiveness of chemoembolization for hepatocellular carcinoma (HCC) with portal vein tumour thrombosis (PVTT) confined to a monosegment of the liver.
A total of 192 treatment-naive patients who received chemoembolization between March 2008 and January 2023 as a first-line treatment for locally advanced HCC with PVTT limited to a monosegment were retrospectively analysed. Overall survival (OS) and the identification of pretreatment risk factors related to OS were investigated using Cox regression analysis. Complications, radiologic tumour response, and progression-free survival (PFS) following chemoembolization were investigated.
After chemoembolization, the 1-, 3-, and 5-year OS rates were 86%, 48%, and 39%, respectively, and the median OS was 33 months. Multivariable analyses revealed four significant pretreatment risk factors: infiltrative HCC (P = .02; HR, 1.60), beyond the up-to-11 criteria (P = .002; HR, 2.26), Child-Pugh class B (P = .01; HR, 2.35), and serum AFP ≥400 ng/mL (P = .01; HR, 1.69). The major complication rate was 5%. Of the 192 patients, 1 month after chemoembolization, 35% achieved a complete response, 47% achieved a partial response, 11% had stable disease, and 7% showed progressive disease. The median PFS after chemoembolization was 12 months.
Chemoembolization shows high safety and efficiency, and contributes to improved survival in patients with HCC with PVTT confined to a monosegment. Four risk factors were found to be significantly associated with improved survival rates after chemoembolization in patients with HCC with PVTT confined to a monosegment.
(1) Although systemic therapy with a combination of atezolizumab and bevacizumab (Atezo-Bev) is recommended as the first-line treatment when HCC invades the portal vein, chemoembolization is not infrequently performed in HCC cases in which tumour burden is limited. (2) Our study cohort (n=192) had a median OS of 33 months and a 5% major complication rate following chemoembolization, findings in the range of candidates typically accepted as ideal for chemoembolization. Thus, patients with HCC with PVTT confined to a monosegment may be good candidates for first-line chemoembolization.
评估局限于肝脏单节段的肝细胞癌(HCC)伴门静脉癌栓(PVTT)患者行化疗栓塞术的安全性和有效性。
回顾性分析了 2008 年 3 月至 2023 年 1 月期间,192 例初次接受化疗栓塞术且局限于肝脏单节段的局部晚期 HCC 伴 PVTT 的患者,将其作为一线治疗方法。采用 Cox 回归分析评估总生存期(OS)和与 OS 相关的术前危险因素。分析化疗栓塞后的并发症、肿瘤反应、无进展生存期(PFS)。
化疗栓塞后,1、3、5 年 OS 率分别为 86%、48%和 39%,中位 OS 为 33 个月。多变量分析显示,4 个术前危险因素与 OS 显著相关:浸润性 HCC(P=0.02;HR,1.60)、超过 up-to-11 标准(P=0.002;HR,2.26)、Child-Pugh 分级 B(P=0.01;HR,2.35)和血清 AFP≥400ng/mL(P=0.01;HR,1.69)。主要并发症发生率为 5%。192 例患者中,化疗栓塞后 1 个月,完全缓解 35%,部分缓解 47%,疾病稳定 11%,疾病进展 7%。化疗栓塞后中位 PFS 为 12 个月。
化疗栓塞术具有较高的安全性和有效性,可改善局限于肝脏单节段的 HCC 伴 PVTT 患者的生存率。发现 4 个危险因素与 HCC 伴 PVTT 局限于肝脏单节段患者化疗栓塞后的生存率显著相关。
(1)当 HCC 侵犯门静脉时,推荐使用阿替利珠单抗联合贝伐珠单抗(Atezo-Bev)进行系统治疗作为一线治疗方法,但化疗栓塞术在肿瘤负荷有限的 HCC 病例中也经常进行。(2)我们的研究队列(n=192)接受化疗栓塞后的中位 OS 为 33 个月,主要并发症发生率为 5%,这一结果在通常被认为是化疗栓塞术理想适应证的范围内。因此,局限于肝脏单节段的 HCC 伴 PVTT 患者可能是化疗栓塞术一线治疗的良好候选者。