Yang Hyun, Woo Hyun Young, Lee Soon Kyu, Han Ji Won, Jang Bohyun, Nam Hee Chul, Lee Hae Lim, Lee Sung Won, Song Do Seon, Song Myeong Jun, Oh Jung Suk, Chun Ho Jong, Jang Jeong Won, Lozada Angelo, Bae Si Hyun, Choi Jong Young, Yoon Seung Kew
Department of Internal Medicine, The Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Internal Medicine and Medical Research Institute, Pusan National University College of Medicine, Pusan, Korea.
Clin Mol Hepatol. 2017 Jun;23(2):128-137. doi: 10.3350/cmh.2016.0071. Epub 2017 May 10.
BACKGROUND/AIMS: Metronomic chemotherapy (MET) is frequently administered in comparatively low doses as a continuous chemotherapeutic agent. The aim of this study was to evaluate the feasibility and overall survival (OS) of MET compared to sorafenib for advanced hepatocellular carcinoma (HCC) patients with portal vein tumor thrombosis (PVTT).
A total of 54 patients with advanced HCC and PVTT who had undergone MET were analyzed between 2005 and 2013. A total of 53 patients who had undergone sorafenib therapy were analyzed as the control group. The primary endpoint of this study was OS.
The median number of MET cycles was two (1-15). The OS values for the MET group and sorafenib group were 158 days (132-184) and 117 days (92-142), respectively (=0.029). The Cox proportional-hazard model showed that a higher risk of death was correlated with higher serum alpha fetoprotein level (≥400 mg/dL, hazard ratio [HR]=1.680, =0.014) and Child-Pugh class B (HR=1.856, =0.008).
MET was associated with more favorable outcomes in terms of overall survival than was sorafenib in patients with advanced HCC with PVTT, especially in patients with poor liver function. Therefore, MET can be considered as a treatment option in patients with advanced HCC with PVTT and poor liver function.
背景/目的:节拍化疗(MET)常以相对低剂量作为持续化疗药物使用。本研究旨在评估与索拉非尼相比,MET用于伴有门静脉癌栓(PVTT)的晚期肝细胞癌(HCC)患者的可行性及总生存期(OS)。
分析2005年至2013年间共54例接受MET治疗的伴有PVTT的晚期HCC患者。将共53例接受索拉非尼治疗的患者作为对照组。本研究的主要终点为OS。
MET的中位周期数为2个(1 - 15个)。MET组和索拉非尼组的OS值分别为158天(132 - 184天)和117天(92 - 142天)(P = 0.029)。Cox比例风险模型显示,较高的死亡风险与较高的血清甲胎蛋白水平(≥400 mg/dL,风险比[HR]=1.680,P = 0.014)及Child-Pugh B级(HR = 1.856,P = 0.008)相关。
对于伴有PVTT的晚期HCC患者,尤其是肝功能较差的患者,MET在总生存期方面比索拉非尼有更有利的结果。因此,MET可被视为伴有PVTT且肝功能较差的晚期HCC患者的一种治疗选择。