Wake Taijiro, Yamada Tomoharu, Tateishi Ryosuke, Moriyama Makoto, Matsushita Yuki, Okushin Kazuya, Nakatsuka Takuma, Sato Masaya, Minami Tatsuya, Kudo Yotaro, Fujishiro Mitsuhiro
Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Cancer Med. 2025 Aug;14(15):e71066. doi: 10.1002/cam4.71066.
Systemic therapy for advanced hepatocellular carcinoma (HCC) includes multi-kinase inhibitors with anti-vascular endothelial growth factor (VEGF) activity and anti-VEGF monoclonal antibodies in combination with immune checkpoint inhibitors. This study aimed to investigate and compare the chronological changes in liver volume between patients who received atezolizumab plus bevacizumab (Atezo/Bev) and those who received lenvatinib.
We enrolled patients who received initial treatment with either Atezo/Bev or lenvatinib for advanced HCC between October 2018 and May 2023. Patients underwent periodic computed tomography (CT) or magnetic resonance imaging (MRI) to evaluate systemic therapy effects. Patients with portal vein thrombosis or prior liver resection/transplantation were excluded. Liver volume was measured at baseline and at 8 and 16 weeks after the initiation of treatment using commercially available software. Liver volume at each time point was expressed as a proportion relative to baseline. A linear regression analysis was used to analyze the chronological changes in liver volume.
Seventy-three patients (40 in the Atezo/Bev group and 33 in the lenvatinib group) were included in this retrospective study. Liver volume decreased in 54 patients (74%) at week 8; the average volume relative to baseline was 0.92 (95% confidence interval: 0.90-0.94, p < 0.01). Liver volume decreased in patients with both shrinking and enlarged tumors. Multivariate analysis indicates that the decrease in nontumoral liver volume was more significant in the lenvatinib group than in the Atezo/Bev group (p = 0.04).
Anti-angiogenic therapy for advanced HCC can lead to liver atrophy.
晚期肝细胞癌(HCC)的全身治疗包括具有抗血管内皮生长因子(VEGF)活性的多激酶抑制剂以及与免疫检查点抑制剂联合使用的抗VEGF单克隆抗体。本研究旨在调查和比较接受阿替利珠单抗联合贝伐单抗(阿替利珠单抗/贝伐单抗)治疗的患者与接受乐伐替尼治疗的患者肝脏体积的时间变化。
我们纳入了2018年10月至2023年5月期间接受阿替利珠单抗/贝伐单抗或乐伐替尼初始治疗晚期HCC的患者。患者接受定期计算机断层扫描(CT)或磁共振成像(MRI)以评估全身治疗效果。排除门静脉血栓形成或既往有肝切除/肝移植史的患者。使用商用软件在基线时以及治疗开始后8周和16周测量肝脏体积。每个时间点的肝脏体积表示为相对于基线的比例。采用线性回归分析来分析肝脏体积的时间变化。
本回顾性研究纳入了73例患者(阿替利珠单抗/贝伐单抗组40例,乐伐替尼组33例)。在第8周时,54例患者(74%)的肝脏体积减小;相对于基线的平均体积为0.92(95%置信区间:0.90-0.94,p<0.01)。肿瘤缩小和增大的患者肝脏体积均减小。多变量分析表明,乐伐替尼组非肿瘤性肝脏体积的减小比阿替利珠单抗/贝伐单抗组更显著(p=0.04)。
晚期HCC的抗血管生成治疗可导致肝脏萎缩。