Department of Liver Surgery, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Collaborative Innovation Center for Cancer Medicine, State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Front Cell Infect Microbiol. 2024 Feb 13;14:1336619. doi: 10.3389/fcimb.2024.1336619. eCollection 2024.
Hepatitis B virus (HBV) reactivation is a common complication in hepatocellular carcinoma (HCC) patients treated with chemotherapy or immunotherapy. This study aimed to evaluate the risk of HBV reactivation and its effect on survival in HCC patients treated with HAIC and lenvatinib plus PD1s.
We retrospectively collected the data of 213 HBV-related HCC patients who underwent HAIC and lenvatinib plus PD1s treatment between June 2019 to June 2022 at Sun Yat-sen University, China. The primary outcome was the risk of HBV reactivation. The secondary outcomes were overall survival (OS), progression-free survival (PFS), and treatment-related adverse events.
Sixteen patients (7.5%) occurred HBV reactivation in our study. The incidence of HBV reactivation was 5% in patients with antiviral prophylaxis and 21.9% in patients without antiviral prophylaxis, respectively. The logistic regression model indicated that for HBV reactivation, lack of antiviral prophylaxis (=0.003) and tumor diameter (=0.036) were independent risk factors. The OS and PFS were significantly shorter in the HBV reactivation group than the non-reactivation group (=0.0023 and =0.00073, respectively). The number of AEs was more in HBV reactivation group than the non-reactivation group, especially hepatic AEs.
HBV reactivation may occur in HCC patients treated with HAIC and lenvatinib plus PD1s. Patients with HBV reactivation had shorter survival time compared with non-reactivation. Therefore, HBV-related HCC patients should undergo antiviral therapy and HBV-DNA monitoring before and during the combination treatment.
乙型肝炎病毒(HBV)再激活是接受化疗或免疫治疗的肝细胞癌(HCC)患者的常见并发症。本研究旨在评估 HCC 患者接受肝动脉化疗栓塞(HAIC)和仑伐替尼联合 PD-1s 治疗后 HBV 再激活的风险及其对生存的影响。
我们回顾性收集了 2019 年 6 月至 2022 年 6 月期间在中国中山大学接受 HAIC 和仑伐替尼联合 PD-1s 治疗的 213 例 HBV 相关 HCC 患者的数据。主要结局是 HBV 再激活的风险。次要结局是总生存期(OS)、无进展生存期(PFS)和治疗相关不良反应。
在我们的研究中,有 16 例(7.5%)患者发生 HBV 再激活。抗病毒预防组的 HBV 再激活发生率为 5%,无抗病毒预防组的 HBV 再激活发生率为 21.9%。Logistic 回归模型表明,对于 HBV 再激活,缺乏抗病毒预防(=0.003)和肿瘤直径(=0.036)是独立的危险因素。HBV 再激活组的 OS 和 PFS 明显短于非再激活组(=0.0023 和=0.00073)。HBV 再激活组的 AEs 数量多于非再激活组,特别是肝 AEs。
接受 HAIC 和仑伐替尼联合 PD-1s 治疗的 HCC 患者可能会发生 HBV 再激活。HBV 再激活患者的生存时间较非再激活患者短。因此,HBV 相关 HCC 患者在联合治疗前和治疗期间应进行抗病毒治疗和 HBV-DNA 监测。