Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Department of Hepatobiliary Pancreatic Surgery, Fujian Provincial Hospital, Fuzhou, China.
Cancer Res Treat. 2024 Oct;56(4):1207-1218. doi: 10.4143/crt.2023.1165. Epub 2024 Apr 30.
The prognosis of patients with hepatocellular carcinoma (HCC) and portal vein tumor thrombus (PVTT) is extremely poor, and systemic therapy is currently the mainstream treatment. This study aimed to assess the efficacy and safety of lenvatinib combined with anti-programmed cell death-1 antibodies and transcatheter arterial chemoembolization (triple therapy) in patients with HCC and PVTT.
This retrospective multicenter study included patients with HCC and PVTT who received triple therapy, were aged between 18 and 75 years, classified as Child-Pugh class A or B, and had at least one measurable lesion. The overall survival (OS), progression-free survival (PFS), objective response rates, and disease control rates were analyzed to assess efficacy. Treatment-related adverse events were analyzed to assess safety profiles.
During a median follow-up of 11.23 months (range, 3.07 to 34.37 months), the median OS was greater than 24 months, and median PFS was 12.53 months. The 2-year OS rate was 54.9%. The objective response rate and disease control rate were 69.8% (74/106) and 84.0% (89/106), respectively; 20.8% (22/106) of the patients experienced grade 3/4 treatment-related adverse events and no treatment-related deaths occurred. The conversion rate to liver resection was 31.1% (33/106), with manageable postoperative complications. The median OS was not reached in the surgery group, but was 19.08 months in the non-surgery group. The median PFS in the surgery and non-surgery groups were 20.50 and 9.00 months, respectively.
Triple therapy showed promising survival benefits and high response rates in patients with HCC and PVTT, with manageable adverse effects.
肝细胞癌(HCC)合并门静脉癌栓(PVTT)患者的预后极差,目前系统治疗是主流治疗方法。本研究旨在评估仑伐替尼联合抗程序性细胞死亡-1 抗体和经导管动脉化疗栓塞(三联疗法)治疗 HCC 和 PVTT 患者的疗效和安全性。
本回顾性多中心研究纳入接受三联疗法的 HCC 和 PVTT 患者,年龄 18~75 岁,Child-Pugh 分级 A 或 B 级,至少有一个可测量的病灶。分析总生存期(OS)、无进展生存期(PFS)、客观缓解率和疾病控制率以评估疗效,分析治疗相关不良反应以评估安全性。
中位随访 11.23 个月(范围 3.07~34.37 个月),中位 OS 大于 24 个月,中位 PFS 为 12.53 个月。2 年 OS 率为 54.9%。客观缓解率和疾病控制率分别为 69.8%(74/106)和 84.0%(89/106);20.8%(22/106)的患者发生 3/4 级治疗相关不良反应,无治疗相关死亡。转化为肝切除术的转化率为 31.1%(33/106),术后并发症可管理。手术组中位 OS 未达到,非手术组为 19.08 个月。手术组和非手术组的中位 PFS 分别为 20.50 和 9.00 个月。
三联疗法在 HCC 和 PVTT 患者中显示出有希望的生存获益和高缓解率,不良反应可管理。