Zheng Shun-Zhen, Liu De-Jie, Sun Ping, Yu Guang-Sheng, Xu Yan-Tian, Gong Wei, Liu Jun
Shun-Zhen Zheng, Guang-Sheng Yu, Yan-Tian Xu, Wei Gong, Jun Liu, Department of Liver Transplantation and Hepatobiliary Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, Shandong Province, China.
World J Gastroenterol. 2014 Nov 21;20(43):16275-81. doi: 10.3748/wjg.v20.i43.16275.
To report the outcome of patients with ruptured hepatocellular carcinoma (HCC) treated at a single center during a 5-year period.
We retrospectively analyzed 32 patients who presented with ruptured HCC at Shandong Provincial Hospital Affiliated to Shandong University between 2008 and 2013.
The mean age of the patients was 53 years (range 39-71 years). Of these patients, 22 received surgical management, 10 underwent transarterial embolization (TAE) or transarterial chemoembolization (TACE), and 12 received sorafenib after surgery, TAE or TACE. Cumulative survival rates at 4, 8 and 12 mo were 72.9%, 50.0% and 33.3%, respectively, in the surgery only group and were 90.0%, 80.6% and 64.1%, respectively, in the surgery plus sorafenib group. Cumulative survival rates at 4, 8 and 12 mo were 68.4%, 43.6% and 19.4%, respectively, in the surgery only or TAE/TACE only groups, and were 91.7%, 75.0% and 60.2%, respectively, in the sorafenib combination groups (P = 0.04). No unexpected side effects due to sorafenib were observed. The most common side effect was hand-foot skin reaction. To date, 5 patients have died. Median follow-up from the start of sorafenib therapy for the remaining 7 patients is 12.7 mo (range 5.8-32.2 mo).
Sorafenib can be used in patients with ruptured HCC as it has interesting activity and is well tolerated; dose adjustment is generally not required. However, a larger prospective study is necessary to determine the efficacy of sorafenib in this group of patients.
报告在一个中心5年期间治疗的肝细胞癌(HCC)破裂患者的治疗结果。
我们回顾性分析了2008年至2013年期间在山东大学附属山东省立医院出现HCC破裂的32例患者。
患者的平均年龄为53岁(范围39 - 71岁)。在这些患者中,22例接受了手术治疗,10例接受了经动脉栓塞(TAE)或经动脉化疗栓塞(TACE),12例在手术、TAE或TACE后接受了索拉非尼治疗。单纯手术组4、8和12个月时的累积生存率分别为72.9%、50.0%和33.3%,手术加索拉非尼组分别为90.0%、80.6%和64.1%。单纯手术组或单纯TAE/TACE组4、8和12个月时的累积生存率分别为68.4%、43.6%和19.4%,索拉非尼联合组分别为91.7%、75.0%和60.2%(P = 0.04)。未观察到索拉非尼引起的意外副作用。最常见的副作用是手足皮肤反应。迄今为止,5例患者已死亡。其余7例患者自索拉非尼治疗开始后的中位随访时间为12.7个月(范围5.8 - 32.2个月)。
索拉非尼可用于HCC破裂患者,因为它具有显著活性且耐受性良好;一般不需要调整剂量。然而,需要进行更大规模的前瞻性研究来确定索拉非尼在这组患者中的疗效。