Goh Myung Ji, Park Hee Chul, Yu Jeong Il, Kang Wonseok, Gwak Geum-Youn, Paik Yong-Han, Lee Joon Hyeok, Koh Kwang Cheol, Paik Seung Woon, Sinn Dong Hyun, Choi Moon Seok
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Liver Cancer. 2023 Feb 10;12(5):467-478. doi: 10.1159/000529635. eCollection 2023 Oct.
We aimed to investigate whether concurrent use of intrahepatic external beam radiotherapy (EBRT) is a viable option for patients with advanced hepatocellular carcinoma (HCC) undergoing tyrosine kinase inhibitor (TKI) therapy.
A total of 453 patients with Barcelona Clinic Liver Cancer stage C (BCLC C) HCC, who started first-line treatment with TKI with intrahepatic EBRT (TKI + RT, = 97) or TKI without intrahepatic EBRT (TKI, = 356) were analyzed. The overall survival (OS) and progression-free survival (PFS) were compared in the overall cohort, patients who received at least 8 weeks of TKI treatment and a propensity score-matched cohort.
OS and PFS were better in those treated with TKI + RT than TKI (8.6 vs. 4.4 months and 4.5 vs. 2.3 months, respectively, with < 0.001). Of note, the TKI + RT group demonstrated significantly longer time to intrahepatic tumor progression. In subgroup analysis, TKI + RT led to better OS than TKI in all subgroups and PFS was significantly improved in patients without extrahepatic metastasis and those with portal vein invasion. There was no significant difference in treatment discontinuation due to adverse events between the TKI + RT and TKI groups (32.0% vs. 37.9%, = 0.34). Furthermore, patients treated with TKI + RT showed better liver function preservation over time compared to TKI without intrahepatic EBRT. Comparable treatment outcomes were observed between patients who received at least 8 weeks of TKI treatment and the propensity score-matched cohort.
Concurrent intrahepatic EBRT targeting the liver and/or macrovascular invasion can be a viable option to improve outcomes of BCLC stage C patients receiving TKI therapy with an aim to control intrahepatic progression and preserving the liver function.
我们旨在研究肝内适形调强放疗(EBRT)与酪氨酸激酶抑制剂(TKI)联合使用对于晚期肝细胞癌(HCC)患者是否是一种可行的选择。
对453例巴塞罗那临床肝癌分期C期(BCLC C)的HCC患者进行分析,这些患者开始接受一线治疗,其中97例接受肝内EBRT联合TKI治疗(TKI + RT),356例接受单纯TKI治疗(TKI)。比较了整个队列、接受至少8周TKI治疗的患者以及倾向评分匹配队列中的总生存期(OS)和无进展生存期(PFS)。
TKI + RT组的OS和PFS均优于TKI组(分别为8.6个月对4.4个月和4.5个月对2.3个月,P < 0.001)。值得注意的是,TKI + RT组肝内肿瘤进展时间明显更长。在亚组分析中,TKI + RT组在所有亚组中的OS均优于TKI组,在无肝外转移和有门静脉侵犯的患者中,PFS显著改善。TKI + RT组和TKI组因不良事件导致治疗中断的情况无显著差异(32.0%对37.9%,P = 0.34)。此外,与未接受肝内EBRT的TKI组相比,接受TKI + RT治疗的患者随着时间推移肝功能保留更好。接受至少8周TKI治疗的患者与倾向评分匹配队列之间观察到类似的治疗结果。
针对肝脏和/或大血管侵犯的肝内EBRT同步治疗可以作为一种可行的选择,以改善接受TKI治疗的BCLC C期患者的预后,旨在控制肝内进展并保留肝功能。