Division of Gastroenterology and Hepatology, Department of Internal Medicine (Omori), School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan.
Department of Medical Biochemistry, Faculty of Pharmaceutical Sciences, Toho University, Chiba, Japan.
Oncology. 2024;102(10):828-840. doi: 10.1159/000537965. Epub 2024 Feb 23.
Atezolizumab plus bevacizumab (AteBev) combination treatment is widely used as first-line systemic therapy for unresectable hepatocellular carcinoma (uHCC). We aimed to clarify therapeutic issues regarding serum cytokines and the immune reaction in patients with uHCC treated with AteBev.
We analyzed preserved serum from a previous prospective study on adult Japanese patients with chronic liver disease and uHCC who received AteBev treatment at our hospital. In that study, AteBev was administered intravenously every 3 weeks, and blood samples were collected before and after 3 weeks' treatment. Dynamic computed tomography was performed after 6 weeks of treatment to assess response.
In the prospective study, 21 of the 59 patients showed partial response (PR) and 19 patients showed stable disease, but 19 patients showed progressive disease (PD). We found that serum levels of tumor necrosis factor-alpha, interleukin (IL)-6, and soluble IL-2 receptor (IL-2R) increased significantly in the PR group, but only soluble IL-2R increased significantly in the PD group. Regulatory T cells decreased significantly in the PD group, but there was no significant change in Th1 or Th2 cells from before to after treatment in any group. As regards soluble MHC-class I, pre-treatment levels were significantly lower in the PD group than in the PR group, and serum levels increased significantly with treatment in the PD group.
These findings reveal a need to further improve T-cell priming and to further make T cells recognize tumor antigens in uHCC.
阿替利珠单抗联合贝伐珠单抗(AteBev)联合治疗被广泛用作不可切除肝细胞癌(uHCC)的一线系统治疗。我们旨在阐明接受 AteBev 治疗的 uHCC 患者血清细胞因子和免疫反应的治疗问题。
我们分析了先前在我院接受 AteBev 治疗的慢性肝病和 uHCC 成年日本患者的前瞻性研究中保存的血清。在该研究中,AteBev 每 3 周静脉给药一次,在治疗前和治疗后 3 周采集血液样本。在治疗 6 周后进行动态计算机断层扫描以评估反应。
在前瞻性研究中,59 例患者中有 21 例显示部分缓解(PR),19 例显示稳定疾病,但 19 例显示进展性疾病(PD)。我们发现 PR 组血清肿瘤坏死因子-α、白细胞介素(IL)-6 和可溶性白细胞介素 2 受体(IL-2R)水平显著升高,但仅 PD 组可溶性 IL-2R 显著升高。PD 组调节性 T 细胞显著减少,但在任何组中,治疗前后 Th1 或 Th2 细胞均无明显变化。关于可溶性 MHC 类 I,PD 组的治疗前水平明显低于 PR 组,且 PD 组的血清水平随着治疗而显著增加。
这些发现表明需要进一步改善 T 细胞的启动,并进一步使 T 细胞识别 uHCC 中的肿瘤抗原。