Department of Radiation Oncology, Senior Department of Oncology, The Fifth Medical Center of PLA General Hospital, Beijing, China.
The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Radiat Oncol. 2023 Jun 12;18(1):101. doi: 10.1186/s13014-023-02270-z.
Patients with hepatocellular carcinoma (HCC) involving portal vein tumor thrombosis (PVTT) are presently lacking effective treatment options. We aimed to compare the efficacy and safety of lenvatinib with or without SBRT for HCC with PVTT.
This retrospective analysis included 37 patients treated with lenvatinib in combination with SBRT and 77 patients treated with lenvatinib alone from August 2018 to August 2021. Overall survival (OS), progression-free survival (PFS), intrahepatic PFS (IHPFS) and objective remission rate (ORR) were compared between the two groups, while adverse events (AEs) was analyzed between the two groups to assess safety profiles.
Median OS, PFS and IHPFS were significantly prolonged in the combination treatment group compared with the single treatment group (median OS, 19.3 vs. 11.2 months, p < 0.001; median PFS: 10.3 vs. 5.3 months, p < 0.001; median IHPFS, 10.7 vs. 5.3 months, p < 0.001). Moreover, a higher ORR (56.8% vs. 20.8%, P < 0.001) were observed in the lenvatinib combined with SBRT group. In subgroup analyses of Vp1-2 and Vp3-4 group, median OS, PFS and IHPFS were also significantly longer in the lenvatinib combined with SBRT group than those in the lenvatinib alone group. AEs in the combined therapy group were mostly manageable and the incidence was not statistically significant compared to the monotherapy group.
Lenvatinib plus SBRT had a significantly better survival benefit than lenvatinib monotherapy in the treatment of HCC patients with PVTT and was well tolerated.
目前,患有肝细胞癌(HCC)合并门静脉癌栓(PVTT)的患者缺乏有效的治疗选择。本研究旨在比较仑伐替尼联合或不联合立体定向放疗(SBRT)治疗 HCC 合并 PVTT 的疗效和安全性。
本回顾性分析纳入了 2018 年 8 月至 2021 年 8 月期间接受仑伐替尼联合 SBRT 治疗的 37 例患者和接受仑伐替尼单药治疗的 77 例患者。比较两组患者的总生存期(OS)、无进展生存期(PFS)、肝内无进展生存期(IHPFS)和客观缓解率(ORR),并分析两组患者的不良反应(AEs)以评估安全性。
与单药治疗组相比,联合治疗组患者的 OS、PFS 和 IHPFS 显著延长(中位 OS,19.3 个月 vs. 11.2 个月,p<0.001;中位 PFS:10.3 个月 vs. 5.3 个月,p<0.001;中位 IHPFS,10.7 个月 vs. 5.3 个月,p<0.001)。此外,联合治疗组的 ORR 更高(56.8% vs. 20.8%,P<0.001)。在 Vp1-2 和 Vp3-4 亚组分析中,联合治疗组患者的 OS、PFS 和 IHPFS 也显著长于单药治疗组。联合治疗组的不良反应大多可管理,且发生率与单药治疗组相比无统计学差异。
仑伐替尼联合 SBRT 治疗 HCC 合并 PVTT 的生存获益明显优于仑伐替尼单药治疗,且耐受性良好。