中华肝胆外科杂志
中華肝膽外科雜誌
중화간담외과잡지
CHINESE JOURNAL OF HEPATOBILIARY SURGERY
2011年
2期
118-122
,共5页
徐威%李敬东%石刚%李建水%戴毅%王小飞
徐威%李敬東%石剛%李建水%戴毅%王小飛
서위%리경동%석강%리건수%대의%왕소비
癌,肝细胞%门静脉高压%上消化道出血%风险因素%预后
癌,肝細胞%門靜脈高壓%上消化道齣血%風險因素%預後
암,간세포%문정맥고압%상소화도출혈%풍험인소%예후
Carcinoma,hepatocellular%Portal hypertension%Upper gastrointestinal haemorrhage%Risk factors%Prognosis
目的 探讨合并门静脉高压症(portal hypertension,PH)的肝细胞癌(hepatocellular carcinoma,HCC)发生上消化道出血的风险因素.方法 回顾性分析2005年1月1日至2009年8月1日收治的231例HCC-PH临床资料.二分类Logistic回归模型行上消化道出血的风险多因素分析.Kaplan-Meier法计算总体生存时间,作Log-rank检验.ROC曲线评估风险因素预测能力.结果 在231例HCC-PH治疗随访共有28例发生上消化道出血,发生后中位生存时间0.8个月(0.10~2.40个月).发生上消化道出血与无上消化道出血者1、2、3年生存率分别为3.57%(1/28)、0%(0/28)、0%(0/28)和21.18%(43/203)、14.29%(29/203)、4.43%(9/203)(P=0.022,0.031,0.605).多因素分析显示AFP界值(P=0.026)和AST≥2N(P=0.004)是HCC-PH发生上消化道出血的风险因素.ROC曲线显示PI≥7.242时,预测HCC-PH发生上消化道的出血灵敏度为81.0%,特异度81.0%,曲线下面积(Area Under the ROC Curve,AUC)为0.828(95%CI,0.698~0.957).不同风险等级病例之间上消化道出血的发生率差异明显(4/151比24/80,P=0.000).结论 上消化道出血是HCC-PH的终末期事件之一,预后不良.AFP界值和AST≥2N是HCC-PH发生上消化道出血的风险因素.风险因素等级划分有助于针对性的筛查和治疗.
目的 探討閤併門靜脈高壓癥(portal hypertension,PH)的肝細胞癌(hepatocellular carcinoma,HCC)髮生上消化道齣血的風險因素.方法 迴顧性分析2005年1月1日至2009年8月1日收治的231例HCC-PH臨床資料.二分類Logistic迴歸模型行上消化道齣血的風險多因素分析.Kaplan-Meier法計算總體生存時間,作Log-rank檢驗.ROC麯線評估風險因素預測能力.結果 在231例HCC-PH治療隨訪共有28例髮生上消化道齣血,髮生後中位生存時間0.8箇月(0.10~2.40箇月).髮生上消化道齣血與無上消化道齣血者1、2、3年生存率分彆為3.57%(1/28)、0%(0/28)、0%(0/28)和21.18%(43/203)、14.29%(29/203)、4.43%(9/203)(P=0.022,0.031,0.605).多因素分析顯示AFP界值(P=0.026)和AST≥2N(P=0.004)是HCC-PH髮生上消化道齣血的風險因素.ROC麯線顯示PI≥7.242時,預測HCC-PH髮生上消化道的齣血靈敏度為81.0%,特異度81.0%,麯線下麵積(Area Under the ROC Curve,AUC)為0.828(95%CI,0.698~0.957).不同風險等級病例之間上消化道齣血的髮生率差異明顯(4/151比24/80,P=0.000).結論 上消化道齣血是HCC-PH的終末期事件之一,預後不良.AFP界值和AST≥2N是HCC-PH髮生上消化道齣血的風險因素.風險因素等級劃分有助于針對性的篩查和治療.
목적 탐토합병문정맥고압증(portal hypertension,PH)적간세포암(hepatocellular carcinoma,HCC)발생상소화도출혈적풍험인소.방법 회고성분석2005년1월1일지2009년8월1일수치적231례HCC-PH림상자료.이분류Logistic회귀모형행상소화도출혈적풍험다인소분석.Kaplan-Meier법계산총체생존시간,작Log-rank검험.ROC곡선평고풍험인소예측능력.결과 재231례HCC-PH치료수방공유28례발생상소화도출혈,발생후중위생존시간0.8개월(0.10~2.40개월).발생상소화도출혈여무상소화도출혈자1、2、3년생존솔분별위3.57%(1/28)、0%(0/28)、0%(0/28)화21.18%(43/203)、14.29%(29/203)、4.43%(9/203)(P=0.022,0.031,0.605).다인소분석현시AFP계치(P=0.026)화AST≥2N(P=0.004)시HCC-PH발생상소화도출혈적풍험인소.ROC곡선현시PI≥7.242시,예측HCC-PH발생상소화도적출혈령민도위81.0%,특이도81.0%,곡선하면적(Area Under the ROC Curve,AUC)위0.828(95%CI,0.698~0.957).불동풍험등급병례지간상소화도출혈적발생솔차이명현(4/151비24/80,P=0.000).결론 상소화도출혈시HCC-PH적종말기사건지일,예후불량.AFP계치화AST≥2N시HCC-PH발생상소화도출혈적풍험인소.풍험인소등급화분유조우침대성적사사화치료.
Objective To explore the risk factors for upper gastrointestinal haemorrhage (UGH) in hepatocellular carcinoma (HCC) with portal hypertension (PH). Methods We retrospectively reviewed the medical records of 231 patients with HCC-PH treated in our Department from 1st January 2005 to 1st August 2009. The clinicopathologic factors were evaluated for their possible association with UGH in univariate analysis followed by multivariate analysis using Logistic regression model. The overall survival (OS) was calculated by the Kaplan-Meier method. Receiver operating characteristics (ROC) analysis with calculation of the area under the curve (AUC), sensitivity, and specificity were carried out to assess the predictive ability of the independent risk factors. Results Among 247 patients diagnosed with HCC-PH, 231 patients met the inclusion criteria and were entered into this study. UGH occurred in 28 patients (12.12 %, 28/231). Patients suffering from UGH had a higher 30-and 60-d mortality when compared with the non UGH group (53.57% vs. 4.43%, 96.43%vs. 10.34%, P<0. 001, 0. 001). The 1-,2-and 3-year overall survival (OS) rates in the non-UGH and the UGH groups were 3. 57% (1/28), 0% (0/28), 0% (0/28) and 21.18% (43/203), 14.29% (29/203), 4.43% (9/203), respectively. There was a trend towards a non-significantly statistical difference in long-term (≥3 yr) survival (P=0. 605). UGH had a dismal prognosis with a median OS of 0. 8 months (0. 10-2. 40 months). Multivariate analysis of the risk factors showed elevated alpha-fetoprotein (AFP) (P = 0. 026) and aspartate aminotransferase (AST) more than twice normal (2N)(P=0. 004) were predictive factors, in particular, AST≥2N. A cutoff value (PI≥7. 242) predicted UGH with an AUC of 0.828 (95%CI, 0.698-0.957), sensitivity of 81.0% and a specificity of 81.0%, as calculated from the ROC. Risk score stratification predicted UGH to show a statistically significant difference (P<0. 001). Conclusions UGH, as one of the end-stage incidents of HCC-PH,had a dismal prognosis. Patients with elevated AFP levels and AST levels above 2N were associated with high risks for UGH and should be monitored carefully or offered prophylactic treatments. Risk score stratification was useful for prediction of UGH.