Yuan Hongjun, Lan Yina, Li Xin, Tang Jing, Liu Fengyong
Department of Interventional Radiology, The First Medical Center of PLA General Hospital 28 Fuxing Road, Beijing 100853, China.
Department of Radiology, The First Medical Center of PLA General Hospital 28 Fuxing Road, Beijing 100853, China.
Am J Cancer Res. 2019 Apr 1;9(4):791-799. eCollection 2019.
The present study aims to investigate retrospectively the efficacy and safety of sorafenib combined with radiofrequency ablation (RFA) to treat unresectable remnant large hepatocellular carcinoma (HCC) after transcatheter arterial chemoembolization (TACE). The 229 consecutive patients with unresectable remnant large HCC (diameter ≥ 5 cm) received RFA and sorafenib (RFA + Sor group, n = 102) or sorafenib (Sor group, n = 127) from January 2010 to January 2016. Complications and overall survival (OS) of the two groups were compared and subgroup analysis carried out. Survival curves were drawn using the Kaplan-Meier method. The RFA + Sor group had no additional serious adverse events. The average OS was 18.3 ± 1.6 months (95% confidence interval [CI]: 15.2-21.4) in the RFA + Sor group and 14.1 ± 1.1 months (95% CI: 11.8-16.3) in the Sor group, a difference the log-rank test indicated was significant (P = 0.03). The 1-, 2- and 3-year survival rates of the RFA + Sor group were 56.9%, 34.3%, and 11.7%, and those of the Sor group were 42.5%, 22.0%, and 5.5%, respectively. The between-group differences in 1- and 2-year survival rates were statistically significant, but not the difference in 3-year survival rates. Subgroup analysis showed that the RFA + Sor group achieved significantly more lifetime benefits than the Sor group in: patients with tumors 5-10 cm in diameter (hazard ratio [HR] 0.42, 95% CI 0.21-1.06 vs. HR 0.94, 95% CI 0.63-1.22); patients with an isolated tumor (HR 0.36, 95% CI 0.19-0.81 vs. HR 0.93, 95% CI 0.55-1.24); and patients with remnant lesion volume < 50% after TACE (HR 0.47, 95% CI 0.21-1.12 vs. HR 0.77, 95% CI 0.46-0.81). RFA with sorafenib is safe and effective for unresectable remnant large HCC, controlling tumor progression and prolonging survival better than sorafenib alone.
本研究旨在回顾性调查索拉非尼联合射频消融(RFA)治疗经动脉化疗栓塞(TACE)后不可切除的残余大肝细胞癌(HCC)的疗效和安全性。2010年1月至2016年1月,229例连续的不可切除残余大HCC(直径≥5 cm)患者接受了RFA联合索拉非尼治疗(RFA + Sor组,n = 102)或索拉非尼治疗(Sor组,n = 127)。比较了两组的并发症和总生存期(OS),并进行了亚组分析。采用Kaplan-Meier法绘制生存曲线。RFA + Sor组未出现额外的严重不良事件。RFA + Sor组的平均OS为18.3±1.6个月(95%置信区间[CI]:15.2 - 21.4),Sor组为14.1±1.1个月(95%CI:11.8 - 16.3),对数秩检验表明差异具有统计学意义(P = 0.03)。RFA + Sor组的1年、2年和3年生存率分别为56.9%、34.3%和11.7%,Sor组分别为42.5%、22.0%和5.5%。两组1年和2年生存率的组间差异具有统计学意义,但3年生存率的差异无统计学意义。亚组分析显示,RFA + Sor组在以下方面比Sor组获得了显著更多的生存益处:直径5 - 10 cm的肿瘤患者(风险比[HR] 0.42,95%CI 0.21 - 1.06 vs. HR 0.94,95%CI 0.63 - 1.22);孤立肿瘤患者(HR 0.36,95%CI 0.19 - 0.81 vs. HR 0.93,95%CI 0.55 - 1.24);TACE后残余病变体积<50%的患者(HR 0.47,95%CI 0.21 - 1.12 vs. HR 0.77,95%CI 0.46 - 0.81)。索拉非尼联合RFA治疗不可切除的残余大HCC安全有效,比单独使用索拉非尼能更好地控制肿瘤进展并延长生存期。