Department of Interventional Oncology, Sun Yat-sen University First Affiliated Hospital, Guangzhou, China.
Department of Ultrasonic, Sun Yat-sen University First Affiliated Hospital, Guangzhou, China.
Cancer Med. 2023 Jan;12(1):61-72. doi: 10.1002/cam4.4937. Epub 2022 Jun 13.
To investigate the efficacy and safety of lenvatinib and idarubicin-loaded drug-eluting beads transarterial chemoembolization (IDADEB-TACE) in primary advanced hepatocellular carcinoma (HCC).
This retrospective study included patients with primary advanced HCC who received either lenvatinib monotherapy or lenvatinib plus IDADEB-TACE as first-line treatment from September 2019 to September 2020 at three institutes. Overall survival (OS), time to progression (TTP), objective response rate (ORR), and adverse events were compared. Propensity score-matching was used to reduce the influence of confounding factors on the outcomes.
The study reviewed 118 patients who received lenvatinib plus IDADEB-TACE (LIDA group) and 182 who received lenvatinib alone (LEN group). After propensity score-matching, 78 pairs of patients remained. Compared to patients in the LEN group, those in the LIDA group had better post-treatment ORR (57.7% vs. 25.6%, p < 0.001, respectively), median OS and TTP (15.7 vs. 11.3 months, hazard ratio [HR] = 0.50, p < 0.001; 8.0 vs. 5.0 months, HR = 0.60, p = 0.003, respectively), 6- and 12-month OS rates (88.5% vs. 71.4%; 67.6% vs. 43.4%, respectively), and progression-free rates at 6 and 12 months (60.3% vs. 42.3%; 21.1% vs. 10.3%, respectively). Vascular invasion, α-fetoprotein level, and treatment type were independent OS predictors, and vascular invasion and treatment type were independent TTP predictors. Incidences of nausea/vomiting, fever, abdominal pain, and increased ALT/AST were higher in the LIDA group than in the LEN group.
Lenvatinib plus IDADEB-TACE is well-tolerated and more effective than lenvatinib monotherapy in patients with advanced HCC.
研究仑伐替尼联合载多柔比星药物洗脱微球经导管肝动脉化疗栓塞术(IDAEB-TACE)在原发性晚期肝细胞癌(HCC)中的疗效和安全性。
本回顾性研究纳入了 2019 年 9 月至 2020 年 9 月在三家医院接受仑伐替尼单药或仑伐替尼联合 IDAEB-TACE 作为一线治疗的原发性晚期 HCC 患者。比较了总生存期(OS)、无进展生存期(TTP)、客观缓解率(ORR)和不良事件。采用倾向评分匹配法以减少混杂因素对结果的影响。
本研究共纳入 118 例接受仑伐替尼联合 IDAEB-TACE(LIDA 组)和 182 例接受仑伐替尼单药(LEN 组)的患者。经倾向评分匹配后,仍有 78 对患者。与 LEN 组相比,LIDA 组患者治疗后 ORR 更高(57.7%比 25.6%,p<0.001),中位 OS 和 TTP 更长(15.7 比 11.3 个月,HR=0.50,p<0.001;8.0 比 5.0 个月,HR=0.60,p=0.003),6 个月和 12 个月 OS 率更高(88.5%比 71.4%;67.6%比 43.4%),6 个月和 12 个月无进展生存率更高(60.3%比 42.3%;21.1%比 10.3%)。血管侵犯、甲胎蛋白水平和治疗类型是 OS 的独立预测因素,血管侵犯和治疗类型是 TTP 的独立预测因素。LIDA 组恶心/呕吐、发热、腹痛和 ALT/AST 升高的发生率高于 LEN 组。
仑伐替尼联合 IDAEB-TACE 治疗晚期 HCC 患者耐受性良好,疗效优于仑伐替尼单药治疗。