Department of Oncology Interventional Therapy, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, No. 160 Pujian Road, Pudong, Shanghai, 200127, People's Republic of China.
Department of Clinical Medicine, Jining Medical College, No. 16 Hehua Street, Jining, Shandong, People's Republic of China.
Cardiovasc Intervent Radiol. 2020 Sep;43(9):1353-1361. doi: 10.1007/s00270-020-02505-6. Epub 2020 May 15.
To evaluate whether anti-CTLA-4 therapy could suppress residual tumor progression and improve survival after insufficient radiofrequency ablation (RFA) in a subcutaneous murine hepatocellular carcinoma (HCC) model.
Forty mice with tumors established on their right flanks were randomly divided into four groups: control group (no treatment), RFA group (insufficient RFA alone), anti-CTLA-4 group (anti-CTLA-4 monotherapy), and RFA + anti-CTLA-4 group (insufficient RFA + anti-CTLA-4). In each group, eight mice were assessed for residual tumors and survival; another two mice were killed on day 14 for histopathologic studies. On day 42, a re-challenge test was performed in the survived mice of RFA + anti-CTLA-4 group to determine whether systemic anti-tumor immunity was established.
The specific growth rate of residual tumors was significantly less in RFA + anti-CTLA-4 group than that of the other three groups (all p < 0.05). The disease control rate was 50% in RFA + anti-CTLA-4 group, while no animals in the other three groups showed disease control. Animals in RFA + anti-CTLA-4 group had longer survival times than those in the other three groups (all p < 0.05). Expression of CD4+ lymphocytes in residual tumors and IFN-γ production in response to H22 tumor cells were significantly higher in RFA + anti-CTLA-4 group than those in the other three groups (all p < 0.05). Three of the five survived mice in RFA + anti-CTLA-4 group underwent tumor re-challenge exhibited tumor rejection.
The present study demonstrated that CTLA-4 blockade injection could suppress the growth of residual tumors and improve survival after insufficient RFA in a subcutaneous murine HCC model.
评估抗 CTLA-4 治疗在皮下鼠肝细胞癌 (HCC) 模型中对射频消融 (RFA) 不足后的残余肿瘤进展和生存的抑制作用。
将 40 只右肋部有肿瘤的小鼠随机分为四组:对照组(无治疗)、RFA 组(单独 RFA 不足)、抗 CTLA-4 组(抗 CTLA-4 单药治疗)和 RFA+抗 CTLA-4 组(RFA 不足+抗 CTLA-4)。每组中,8 只用于评估残余肿瘤和生存情况;另外 2 只在第 14 天处死进行组织病理学研究。在 RFA+抗 CTLA-4 组的幸存小鼠中,于第 42 天进行再挑战试验,以确定是否建立了全身抗肿瘤免疫。
RFA+抗 CTLA-4 组的残余肿瘤的特异性生长率明显低于其他三组(均 p<0.05)。RFA+抗 CTLA-4 组的疾病控制率为 50%,而其他三组均无疾病控制。RFA+抗 CTLA-4 组的动物存活时间长于其他三组(均 p<0.05)。RFA+抗 CTLA-4 组的残余肿瘤中 CD4+淋巴细胞的表达和对 H22 肿瘤细胞的 IFN-γ 产生明显高于其他三组(均 p<0.05)。RFA+抗 CTLA-4 组的 5 只幸存小鼠中有 3 只在再挑战时出现肿瘤排斥。
本研究表明,CTLA-4 阻断注射可抑制皮下鼠 HCC 模型中 RFA 不足后的残余肿瘤生长和提高生存。