Azzaroli Francesco, Accogli Esterita, Nigro Giovanni, Trere Davide, Giovanelli Silvia, Miracolo Anna, Lodato Francesca, Montagnani Marco, Tamé Mariarosa, Colecchia Antonio, Mwangemi Constance, Festi Davide, Roda Enrico, Derenzini Massimo, Mazzella Giuseppe
Department of Internal Medicine, University of Bologna, Via Massarenti 9, 40138 Bologna.
World J Gastroenterol. 2004 Nov 1;10(21):3099-102. doi: 10.3748/wjg.v10.i21.3099.
To determine the role of interferon (IFN) with or without ribavirin in preventing or delaying hepatocellular carcinoma (HCC) development in patients with hepatitis C virus (HCV) related cirrhosis. Data on the preventive effect of IFN plus ribavirin treatment are lacking.
A total of 101 patients (62 males and 39 females, mean age 55.1+/-1.4 years) with histologically proven HCV related liver cirrhosis plus compatible biochemistry and ultrasonography were enrolled in the study. Biochemistry and ultrasonography were performed every 6 mo. Ultrasound guided liver biopsy was performed on all detected focal lesions. Follow-up lasted for 5 years. Cellular proliferation, evaluated by measuring Ag-NOR proteins in hepatocytes nuclei, was expressed as AgNOR-Proliferative index (AgNOR-PI) (cut-off = 2.5). Forty-one patients (27 males, 14 females) were only followed up after the end of an yearly treatment with IFN-alpha2b (old treatment control group = OTCG). Sixty naive patients were stratified according to sex and AgNOR-PI and then randomized in two groups: 30 were treated with IFN-alpha2b + ribavirin (treatment group = TG), the remaining were not treated (control group = CG). Nonresponders (NR) or relapsers in the TG received further IFN/ribavirin treatments after a 6 mo of withdrawal.
AgNOR-PI was significantly lowered by IFN (P<0.001). HCC incidence was higher in patients with AgNOR-PI>2.5 (26% vs 3%, P<0.01). Two NR in the OTCG, none in the TG and 9 patients in the CG developed HCC during follow-up. The Kaplan-Mayer survival curves showed statistically significant differences both between OTCG and CG (P<0.004) and between TG and CG (P<0.003).
IFN/ribavirin treatment associated with re-treatment courses of NR seems to produce the best results in terms of HCC prevention. AgNOR-PI is a useful marker of possible HCC development.
确定干扰素(IFN)联合或不联合利巴韦林在预防或延缓丙型肝炎病毒(HCV)相关肝硬化患者肝细胞癌(HCC)发生中的作用。关于IFN加利巴韦林治疗预防效果的数据尚缺乏。
共有101例经组织学证实为HCV相关肝硬化且生化及超声检查结果相符的患者(62例男性,39例女性,平均年龄55.1±1.4岁)纳入本研究。每6个月进行一次生化及超声检查。对所有检测到的局灶性病变进行超声引导下肝活检。随访持续5年。通过测量肝细胞核中的Ag-NOR蛋白评估细胞增殖,以AgNOR增殖指数(AgNOR-PI)表示(临界值 = 2.5)。41例患者(27例男性,14例女性)在接受α-2b干扰素年度治疗结束后仅进行随访(旧治疗对照组 = OTCG)。60例初治患者根据性别和AgNOR-PI分层,然后随机分为两组:30例接受α-2b干扰素 + 利巴韦林治疗(治疗组 = TG),其余未接受治疗(对照组 = CG)。治疗组中的无应答者(NR)或复发者在停药6个月后接受进一步的IFN/利巴韦林治疗。
IFN可显著降低AgNOR-PI(P<0.001)。AgNOR-PI>2.5的患者HCC发生率更高(26% 对3%,P<0.01)。旧治疗对照组中有2例无应答者、治疗组中无、对照组中有9例患者在随访期间发生HCC。Kaplan-Mayer生存曲线显示,旧治疗对照组与对照组之间(P<0.004)以及治疗组与对照组之间(P<0.003)均存在统计学显著差异。
IFN/利巴韦林治疗联合对无应答者的再治疗疗程似乎在预防HCC方面产生最佳效果。AgNOR-PI是可能发生HCC的有用标志物。