Center for Liver Cancer, National Cancer Center, Goyang, Korea.
J Gastroenterol Hepatol. 2012 Jun;27(6):1051-6. doi: 10.1111/j.1440-1746.2011.06963.x.
Patients with hepatocellular carcinoma (HCC) that is refractory to repeated transarterial chemoembolization (TACE) are considered for systemic therapy, but TACE refractoriness is not well defined. The aim of this study was to determine the characteristics of patients whose HCC is refractory to repetitive TACE.
We evaluated 264 patients with intermediate-stage HCC who underwent TACE between January 2006 and September 2009. We designated the development of vascular invasion or extrahepatic spread during follow up as "stage progression" (SP), and hypothesized that SP might be the surrogate end-point for TACE refractoriness.
The median follow up was 18.2 months, and median number of TACE was 3.0 (range, 1-13). Median time-to-progression was 5.5 months (95% confidence interval, 4.8-6.2), and median overall survival was 25.3 months (95% confidence interval, 21.6-29.0). We classified the patients according to disease course as: no progressive disease (PD(-); n = 33); PD without SP (PD(+)SP(-); n = 113); PD followed by SP (PD→SP; n = 47); and simultaneous PD and SP (PD&SP; n = 64). PD(-) and PD(+)SP(-) groups showed no difference in overall survival, PD→SP group had worse overall survival than PD(-) and PD(+)SP(-) groups, and PD&SP group had the worst overall survival. The significant prognostic factors for SP-free survival were development of PD and need for three sessions of TACE during the first 6 months.
SP-free survival can be regarded as an end-point for TACE refractoriness. Development of progression or need for three sessions of TACE within the first 6 months could be predictive of TACE refractoriness.
对于多次经动脉化疗栓塞(TACE)治疗无效的肝细胞癌(HCC)患者,考虑采用系统治疗,但 TACE 耐药性尚未明确。本研究旨在确定 HCC 对重复 TACE 耐药患者的特征。
我们评估了 2006 年 1 月至 2009 年 9 月期间接受 TACE 治疗的 264 例中期 HCC 患者。我们将随访期间血管侵犯或肝外转移的发展定义为“阶段进展”(SP),并假设 SP 可能是 TACE 耐药的替代终点。
中位随访时间为 18.2 个月,中位 TACE 次数为 3.0(范围 1-13)。中位无进展生存期为 5.5 个月(95%置信区间,4.8-6.2),中位总生存期为 25.3 个月(95%置信区间,21.6-29.0)。我们根据疾病进程将患者分为:无进展疾病(PD(-);n=33);无 SP 的 PD(PD(+)SP(-);n=113);PD 后继发 SP(PD→SP;n=47);和同时 PD 和 SP(PD&SP;n=64)。PD(-)和 PD(+)SP(-)组的总生存期无差异,PD→SP 组的总生存期较 PD(-)和 PD(+)SP(-)组差,而 PD&SP 组的总生存期最差。SP 无进展生存期的显著预后因素是进展的发生和前 6 个月内需要 3 次 TACE 治疗。
SP 无进展生存期可作为 TACE 耐药的终点。前 6 个月内进展或需要 3 次 TACE 治疗可预测 TACE 耐药。