Kuwano Akifumi, Yada Masayoshi, Narutomi Fumiya, Nagasawa Shigehiro, Tanaka Kosuke, Kurosaka Kazuki, Ohishi Yoshihiro, Masumoto Akihide, Motomura Kenta
Department of Hepatology, Iizuka Hospital, Iizuka, Fukuoka 820-8505, Japan.
Department of Diagnostic Pathology, Iizuka Hospital, Iizuka, Fukuoka 820-8505, Japan.
Oncol Lett. 2022 May 18;24(1):216. doi: 10.3892/ol.2022.13337. eCollection 2022 Jul.
Atezolizumab plus bevacizumab therapy has high response rates in patients with advanced hepatocellular carcinoma (HCC). It has been reported that HCC with immune exclusion associated with the signal activation of WNT/β-catenin is resistant to immune checkpoint inhibitors; however, to the best of our knowledge, the effectiveness of atezolizumab plus bevacizumab for HCC with WNT/β-catenin signal activation has not been reported. The present study aimed to analyze the efficacy of atezolizumab plus bevacizumab for HCC with WNT/β-catenin signal activation. A total of 24 patients who underwent liver tumor biopsy for HCC were classified into WNT/β-catenin signal activation and inactivation groups according to the expression levels of β-catenin and glutamine synthetase, which are indicative of WNT/β-catenin signal activation. The differences in the clinical responses to treatment between the groups were analyzed. A total of 15 patients had HCC with WNT/β-catenin signal activation, whereas 9 patients had HCC with WNT/β-catenin signal inactivation. There were no significant differences between both groups regarding objective responses (P=0.519) and disease control (P=0.586). In the WNT/β-catenin signal activation group, the median progression-free survival rate was 6.9 months compared with 6.2 months in the WNT/β-catenin signal inactivation group (P=0.674). Although a small number of patients was included in the present study, the present findings suggested that the efficacy of atezolizumab plus bevacizumab might be unaffected by WNT/β-catenin signal activation.
阿替利珠单抗联合贝伐单抗治疗晚期肝细胞癌(HCC)患者具有较高的缓解率。据报道,与WNT/β-连环蛋白信号激活相关的免疫排除型HCC对免疫检查点抑制剂耐药;然而,据我们所知,阿替利珠单抗联合贝伐单抗对WNT/β-连环蛋白信号激活的HCC的有效性尚未见报道。本研究旨在分析阿替利珠单抗联合贝伐单抗对WNT/β-连环蛋白信号激活的HCC的疗效。对24例行HCC肝肿瘤活检的患者,根据指示WNT/β-连环蛋白信号激活的β-连环蛋白和谷氨酰胺合成酶的表达水平,分为WNT/β-连环蛋白信号激活组和失活组。分析两组间治疗临床反应的差异。共有15例患者的HCC存在WNT/β-连环蛋白信号激活,而9例患者的HCC存在WNT/β-连环蛋白信号失活。两组在客观缓解(P=0.519)和疾病控制(P=0.586)方面无显著差异。在WNT/β-连环蛋白信号激活组,中位无进展生存率为6.9个月,而WNT/β-连环蛋白信号失活组为6.2个月(P=0.674)。尽管本研究纳入的患者数量较少,但目前的研究结果表明,阿替利珠单抗联合贝伐单抗的疗效可能不受WNT/β-连环蛋白信号激活的影响。