Li Guangxin, Zhao Ying, Li Keren, Yang Shizhong, Xiang Canhong, Song Jiyong, Yang Yanmei, Li Gong, Dong Jiahong
Department of Radiation Oncology, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, People's Republic of China.
Hepatopancereatobiliary Center, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, People's Republic of China.
J Hepatocell Carcinoma. 2023 Nov 9;10:2037-2048. doi: 10.2147/JHC.S432542. eCollection 2023.
BACKGROUND: Patients with hepatocellular carcinoma (HCC) with portal vein tumour thrombus (PVTT), especially type Vp-4, usually have a poor prognosis. However, the vast majority of Phase III clinical trials exclude this population based on the inclusion criteria. Lenvatinib plus a PD-1 inhibitor has shown promising antitumour activity and tolerable safety in patients with unresectable HCC in Asian populations. Radiotherapy has also demonstrated high response rates and favourable survival for HCC patients with PVTT. This study aimed to explore the preliminary clinical efficacy and safety of lenvatinib plus the PD-1 inhibitor combined with radiotherapy for HCC patients with main portal vein tumour thrombus. METHODS: Between 1 March 2018 and 31 October 2020, HCC patients with main PVTT who received lenvatinib plus a PD-1 inhibitor (pembrolizumab, nivolumab or sintilimab) combined with radiotherapy from Beijing Tsinghua Changgung Hospital in China were reviewed for eligibility. The efficacy was evaluated by the survival and PVTT response rate, and the safety was evaluated by the frequency of key adverse events (AEs). RESULTS: In total, 39 eligible HCC patients with type Vp-4 PVTT who received triple therapy were included in this study. The 2-year OS rate was 15.4%, which was the primary end-point of our study. The median overall survival (OS) and progression-free survival (PFS) were 9.4 months (range 2.3 to 57.1) and 4.9 months (range 1.4 to 36.1), respectively. The objective response rate (ORR) of PVTT based on mRECIST was 61.5%. AFP dropped to normal 3 months after radiotherapy and was an independent risk factor associated with OS. All AEs were controlled, and no treatment-related deaths occurred. CONCLUSION: Lenvatinib plus PD-1 inhibitor combined with radiotherapy had a significant therapeutic effect and manageable AEs in HCC patients with type Vp-4 PVTT and may be a potential treatment option for advanced HCC.
背景:伴有门静脉癌栓(PVTT)的肝细胞癌(HCC)患者,尤其是Vp-4型患者,通常预后较差。然而,绝大多数III期临床试验基于纳入标准将该人群排除在外。在亚洲人群中,乐伐替尼联合PD-1抑制剂已显示出对不可切除HCC患者有良好的抗肿瘤活性和可耐受的安全性。放射治疗对伴有PVTT的HCC患者也显示出高缓解率和良好的生存率。本研究旨在探讨乐伐替尼联合PD-1抑制剂并联合放疗用于伴有主要门静脉癌栓的HCC患者的初步临床疗效和安全性。 方法:回顾性分析2018年3月1日至2020年10月31日期间在中国北京清华长庚医院接受乐伐替尼联合PD-1抑制剂(帕博利珠单抗、纳武利尤单抗或信迪利单抗)并联合放疗的伴有主要PVTT的HCC患者的入选资格。通过生存率和PVTT缓解率评估疗效,通过关键不良事件(AE)的发生频率评估安全性。 结果:本研究共纳入39例接受三联疗法的符合条件的Vp-4型PVTT的HCC患者。2年总生存率为15.4%,这是我们研究的主要终点。中位总生存期(OS)和无进展生存期(PFS)分别为9.4个月(范围2.3至57.1个月)和4.9个月(范围1.4至36.1个月)。基于mRECIST的PVTT客观缓解率为61.5%。放疗3个月后甲胎蛋白降至正常,且是与OS相关的独立危险因素。所有AE均得到控制,未发生与治疗相关的死亡。 结论:乐伐替尼联合PD-1抑制剂并联合放疗对Vp-4型PVTT的HCC患者有显著治疗效果且AE可控,可能是晚期HCC的一种潜在治疗选择。
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