Zhang X F, Liu Y, Li J H, Lei P, Zhang X Y, Wan Z, Lei T, Zhang N, Wu X N, Long Z D, Li Z F, Wang B, Liu X M, Wu Z, Chen X, Wang J X, Yuan P, Li Y, Zhou J, Pawlik M, Lyu Y
Department of Hepatobiliary Surgery,the First Affiliated Hospital of Xi'an Jiaotong University;Institute of Advanced Surgical Technology and Engineering,Xi'an Jiaotong University;National-Local Joint Engineering Research Center for Precision Surgery and Regenerative Medicine,Xi'an 710061,China.
Department of General Surgery,the Second Affiliated Hospital of Xi'an Jiaotong University,Xi'an 710004,China.
Zhonghua Wai Ke Za Zhi. 2021 Oct 1;59(10):821-828. doi: 10.3760/cma.j.cn112139-20210713-00308.
To identify whether splenectomy for treatment of hypersplenism has any impact on development of hepatocellular carcinoma(HCC) among patients with liver cirrhosis and hepatitis. Patients who underwent splenectomy for hypersplenism secondary to liver cirrhosis and portal hypertension between January 2008 and December 2012 were included from seven hospitals in China, whereas patients receiving medication treatments for liver cirrhosis and portal hypertension (non-splenectomy) at the same time period among the seven hospitals were included as control groups. In the splenectomy group, all the patients received open or laparoscopic splenectomy with or without pericardial devascularization. In contrast, patients in the control group were treated conservatively for liver cirrhosis and portal hypertension with medicines (non-splenectomy) with no invasive treatments, such as transjugular intrahepatic portosystemic shunt, splenectomy or liver transplantation before HCC development. All the patients were routinely screened for HCC development with abdominal ultrasound, liver function and alpha-fetoprotein every 3 to 6 months. To minimize the selection bias, propensity score matching (PSM) was used to match the baseline data of patients among splenectomy versus non-splenectomy groups. The Kaplan-Meier method was used to calculate the overall survival and cumulative incidence of HCC development, and the Log-rank test was used to compare the survival or disease rates between the two groups. Univariate and Cox proportional hazard regression models were used to analyze the potential risk factors associated with development of HCC. A total of 871 patients with liver cirrhosis and hypertension were included synchronously from 7 tertiary hospitals. Among them, 407 patients had a history of splenectomy for hypersplenism (splenectomy group), whereas 464 patients who received medical treatment but not splenectomy (non-splenectomy group). After PSM,233 pairs of patients were matched in adjusted cohorts. The cumulative incidence of HCC diagnosis at 1,3,5 and 7 years were 1%,6%,7% and 15% in the splenectomy group, which was significantly lower than 1%,6%,15% and 23% in the non-splenectomy group (=0.53,95%:0.31 to 0.91,=0.028). On multivariable analysis, splenectomy was independently associated with decreased risk of HCC development (=0.55,0.32 to 0.95,=0.031). The cumulative survival rates of all the patients at 1,3,5,and 7 years were 100%,97%,91%,86% in the splenectomy group,which was similar with that of 100%,97%,92%,84% in the non-splenectomy group (=0.899). In total,49 patients (12.0%) among splenectomy group and 75 patients (16.2%) in non-splenectomy group developed HCC during the study period, respectively. Compared to patients in non-splenectomy group, patients who developed HCC after splenectomy were unlikely to receive curative resection for HCC (12.2% 33.3%,χ²=7.029, =0.008). Splenectomy for treatment of hypersplenism may decrease the risk of HCC development among patients with liver cirrhosis and portal hypertension.
为确定脾切除术治疗脾功能亢进对肝硬化和肝炎患者肝细胞癌(HCC)发生发展是否有影响。纳入2008年1月至2012年12月期间在中国7家医院因肝硬化和门静脉高压继发脾功能亢进而行脾切除术的患者,同时将同期在这7家医院接受肝硬化和门静脉高压药物治疗(未行脾切除术)的患者作为对照组。脾切除组所有患者均接受开放或腹腔镜脾切除术,伴或不伴贲门周围血管离断术。相比之下,对照组患者采用药物保守治疗肝硬化和门静脉高压(未行脾切除术),在发生HCC之前未接受诸如经颈静脉肝内门体分流术、脾切除术或肝移植等侵入性治疗。所有患者每3至6个月定期接受腹部超声、肝功能及甲胎蛋白检查以筛查HCC发生情况。为尽量减少选择偏倚,采用倾向评分匹配(PSM)对脾切除组与非脾切除组患者的基线数据进行匹配。采用Kaplan-Meier法计算HCC发生的总生存率和累积发病率,并采用Log-rank检验比较两组的生存率或疾病发生率。采用单因素和Cox比例风险回归模型分析与HCC发生相关的潜在危险因素。共从7家三级医院同步纳入871例肝硬化和高血压患者。其中,407例患者有因脾功能亢进行脾切除术史(脾切除组),464例患者接受药物治疗但未行脾切除术(非脾切除组)。经过PSM后,在调整队列中匹配了233对患者。脾切除组1年、3年、5年和7年HCC诊断的累积发病率分别为1%、6%、7%和15%,显著低于非脾切除组的1%、6%、15%和23%(P=0.53,95%CI:0.31至0.91,P=0.028)。多因素分析显示,脾切除术与HCC发生风险降低独立相关(P=0.55,0.32至0.95,P=0.031)。脾切除组所有患者1年、3年、5年和7年的累积生存率分别为100%、97%、91%、86%,与非脾切除组的100%、97%、92%、84%相似(P=0.899)。在研究期间,脾切除组共有49例患者(12.0%)发生HCC,非脾切除组有75例患者(16.2%)发生HCC。与非脾切除组患者相比,脾切除术后发生HCC的患者不太可能接受HCC根治性切除术(12.2%对33.3%,χ²=7.029,P=0.008)。脾切除术治疗脾功能亢进可能降低肝硬化和门静脉高压患者HCC发生风险。