Department of Surgery, Division of Hepato-Biliary-Pancreatic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Surgery, Division of Hepato-Biliary-Pancreatic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan;
Anticancer Res. 2023 Feb;43(2):911-918. doi: 10.21873/anticanres.16234.
BACKGROUND/AIM: The chemotherapeutic landscape for hepatocellular carcinomas (HCCs) has changed dramatically with the availability of several treatment options. This study aimed to assess the long-term outcomes of lenvatinib treatment and analyze its feasibility in the sequential treatment of HCCs.
Eighty-five consecutive patients who received lenvatinib for unresectable HCCs were investigated retrospectively. Survival was assessed based on when the patients were first radiologically diagnosed with progressive disease. Among those with radiologically diagnosed stable or progressive disease at 3 months after lenvatinib administration, the cutoff α-fetoprotein (AFP) ratio (ratio of the AFP level after lenvatinib treatment to the pretreatment AFP level) that was predictive of survival was determined using receiver operating characteristic analysis.
The median survival time (MST) was significantly worse among patients diagnosed with progressive disease at 1 month after treatment than among those diagnosed at 2-3 or 3-4 months after treatment [MSTs at 1, 2-3, and 3-4 months: 2.2, 10.2, and 17.3 months, respectively (p<0.001)]. An AFP ratio of 1.36 (computed using the AFP level at 3 months after lenvatinib treatment) was significantly predictive of survival in patients with stable or progressive disease (26.3 vs. 11.3 months, p=0.0024).
The prognosis of patients on lenvatinib who develop early progressive disease is dismal. Thus, their treatment should be ceased or switched. The 3-month AFP ratio of 1.36 may be a potentially useful cutoff for considering a switch to other treatments in patients radiologically diagnosed with stable or progressive disease.
背景/目的:随着多种治疗方案的出现,肝细胞癌(HCC)的化疗格局发生了巨大变化。本研究旨在评估仑伐替尼治疗的长期疗效,并分析其在 HCC 序贯治疗中的可行性。
回顾性分析 85 例接受仑伐替尼治疗不可切除 HCC 的连续患者。根据患者首次影像学诊断为疾病进展时评估生存情况。对于仑伐替尼治疗 3 个月后影像学诊断为稳定或进展性疾病的患者,使用受试者工作特征分析确定预测生存的截断α-胎蛋白(AFP)比值(AFP 水平在仑伐替尼治疗后的比值与治疗前 AFP 水平)。
治疗后 1 个月诊断为进展性疾病的患者中位生存时间(MST)明显差于治疗后 2-3 个月或 3-4 个月诊断为进展性疾病的患者[1、2-3 和 3-4 个月的 MST 分别为 2.2、10.2 和 17.3 个月(p<0.001)]。仑伐替尼治疗后 3 个月 AFP 比值为 1.36(计算方法为 AFP 水平)与稳定或进展性疾病患者的生存显著相关(26.3 与 11.3 个月,p=0.0024)。
早期进展的仑伐替尼患者预后较差,应停止或更换治疗方案。3 个月 AFP 比值为 1.36 可能是影像学诊断为稳定或进展性疾病的患者考虑转为其他治疗的潜在有用截止值。