Anti-Angiogenic Agents for Advanced Hepatocellular Carcinoma Induce Liver Atrophy

IF 2.9 2区 医学 Q2 ONCOLOGY
Cancer Medicine Pub Date : 2025-07-25 DOI:10.1002/cam4.71066
Taijiro Wake, Tomoharu Yamada, Ryosuke Tateishi, Makoto Moriyama, Yuki Matsushita, Kazuya Okushin, Takuma Nakatsuka, Masaya Sato, Tatsuya Minami, Yotaro Kudo, Mitsuhiro Fujishiro
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引用次数: 0

Abstract

Aim

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.

Methods

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.

Results

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).

Conclusions

Anti-angiogenic therapy for advanced HCC can lead to liver atrophy.

Abstract Image

晚期肝癌抗血管生成药物诱导肝萎缩
目的晚期肝癌(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和抗VEGF单克隆抗体联合免疫检查点抑制剂。本研究旨在调查和比较接受atezolizumab加贝伐单抗(Atezo/Bev)和接受lenvatinib的患者肝脏体积的时间变化。方法:纳入2018年10月至2023年5月期间接受Atezo/Bev或lenvatinib初始治疗的晚期HCC患者。患者定期接受计算机断层扫描(CT)或磁共振成像(MRI)来评估全身治疗的效果。排除有门静脉血栓形成或既往肝切除/移植的患者。使用市售软件在基线和治疗开始后8周和16周测量肝脏体积。每个时间点的肝脏体积以相对于基线的比例表示。采用线性回归分析肝容量的时间变化。结果本研究共纳入73例患者(Atezo/Bev组40例,lenvatinib组33例)。第8周,54例(74%)患者肝脏体积减小;相对于基线的平均体积为0.92(95%可信区间:0.90-0.94,p < 0.01)。肿瘤缩小和增大的患者肝脏体积均减小。多因素分析显示lenvatinib组非肿瘤肝体积的减少比Atezo/Bev组更显著(p = 0.04)。结论抗血管生成治疗晚期肝癌可导致肝萎缩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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