Chan Kun-Ming, Lai Yin, Hung Hao-Chien, Lee Jin-Chiao, Cheng Chih-Hsien, Wang Yu-Chao, Wu Tsung-Han, Lee Chen-Fang, Wu Ting-Jung, Chou Hong-Shiue, Wang Ching-Ting, Chai Pei-Mei, Lien Hsin-Yi, Lee Wei-Chen
Department of General Surgery and Chang Gung Transplantation Institute, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Department of Nursing, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
J Hepatocell Carcinoma. 2023 Feb 18;10:281-290. doi: 10.2147/JHC.S393964. eCollection 2023.
Tyrosine kinase inhibitors (TKIs) remain the primary therapeutic option for patients with advanced-stage hepatocellular carcinoma (HCC). However, the selection of a suitable TKI is an issue in real-world clinical practice. Thus, this study aimed to identify patients most likely to benefit from lenvatinib treatment.
A retrospective review of 143 patients with unresectable advanced-stage HCC treated with lenvatinib between January 2020 and December 2021 was performed. Outcomes related to lenvatinib treatment were measured, and the clinical parameters affecting prognosis were analyzed.
Overall, the median time of progression-free survival (PFS) and overall survival (OS) were 7.1 months and 17.7 months, respectively. Prognostic analyses found that Child-Pugh score > 5 (hazard ratio [HR] = 2.43, 95% confidence interval [CI] = 1.55-3.80, = 0.001) was a significant factor affecting the PFS of HCC after lenvatinib treatment. Child-Pugh score > 5 (HR = 2.12, 95% CI = 1.20-3.74, = 0.009), body weight ≥ 60 kg (HR = 0.54, 95% CI = 0.32-0.90, = 0.020), and additional trans-arterial chemoembolization (TACE) treatment (HR = 0.38, 95% CI = 0.21-0.70, = 0.003) were significant prognostic factors for OS. However, early α-fetoprotein reduction was not significantly correlated with patient outcomes. Additionally, patients with pre-treatment neutrophil-lymphocyte ratio > 4.07 showed a significant worse PFS and OS than other patients.
The outcome of patients with advanced-stage HCC remains poor. However, the host condition, including good physical status and better functional liver preservation, largely affected the outcome of patients receiving lenvatinib treatment. Moreover, additional locoregional therapy for intrahepatic HCC, other than TKI treatment, can be considered in certain patients to achieve a favorable outcome.
酪氨酸激酶抑制剂(TKIs)仍然是晚期肝细胞癌(HCC)患者的主要治疗选择。然而,在实际临床实践中,选择合适的TKI是一个问题。因此,本研究旨在确定最有可能从乐伐替尼治疗中获益的患者。
对2020年1月至2021年12月期间接受乐伐替尼治疗的143例不可切除晚期HCC患者进行回顾性研究。测量与乐伐替尼治疗相关的结果,并分析影响预后的临床参数。
总体而言,无进展生存期(PFS)和总生存期(OS)的中位数分别为7.1个月和17.7个月。预后分析发现,Child-Pugh评分>5(风险比[HR]=2.43,95%置信区间[CI]=1.55-3.80,P=0.001)是影响乐伐替尼治疗后HCC患者PFS的重要因素。Child-Pugh评分>5(HR=2.12,95%CI=1.20-3.74,P=0.009)、体重≥60 kg(HR=0.54,95%CI=0.32-0.90,P=0.020)以及额外的经动脉化疗栓塞(TACE)治疗(HR=0.38,95%CI=0.21-0.70,P=0.003)是OS的重要预后因素。然而,早期甲胎蛋白降低与患者预后无显著相关性。此外,治疗前中性粒细胞与淋巴细胞比值>4.07的患者的PFS和OS明显比其他患者差。
晚期HCC患者的预后仍然很差。然而,包括良好身体状况和更好的肝功能保留在内的宿主状况在很大程度上影响了接受乐伐替尼治疗患者的预后。此外,对于肝内HCC,除TKI治疗外,某些患者可考虑额外的局部区域治疗以获得良好预后。