Papatheodoridis G V, Katsoulidou A, Touloumi G, Delladetsima J K, Hatzakis A, Tassopoulos N C
First Department of Medicine, Western Attica General Hospital, Athens, Greece.
Eur J Gastroenterol Hepatol. 1996 May;8(5):469-75.
To evaluate the biochemical and virological response in chronic hepatitis C patients treated with interferon-alpha at the usual dosage of 3 MU thrice weekly for 6 or 12 months, and to analyse the significance of clearance of serum HCV RNA and of HCV genotype in the prediction of sustained biochemical remission.
Liver Unit, Western Attica General Hospital, Athens, Greece.
Sixty consecutive patients with histologically confirmed chronic hepatitis C.
All patients received interferon-alpha-2b in a dose of 3 MU thrice weekly for 6 (n = 26) or 12 (n = 34) months. Serial serum samples were retrospectively tested for the presence of HCV RNA by a polymerase chain reaction assay and pretreatment serum samples for the determination of HCV genotype.
Sustained biochemical response rate was significantly higher in the 12-month group (62% vs. 35%, P = 0.037). Clearance of serum HCV RNA at the end of treatment was achieved in 33 (58.9%) of the 56 patients with detectable pretreatment HCV RNA. HCV RNA reappeared in serum significantly more often in patients treated for 6 than for 12 months (35.7% vs. 5.3%, P = 0.037). Serum HCV RNA after 6 months of therapy was a prognostic factor of sustained biochemical response, which was observed in 75% of the HCV RNA-negative and in only 16.7% of the HCV RNA-positive patients (OR 0.067, P < 0.001). Moreover, in patients negative for HCV RNA after 6 months of therapy, 12 months' treatment resulted in a higher sustained response rate than did 6 months' (89% vs. 57%, P = 0.05). HCV genotype 1 was associated with a significantly lower sustained response rate (30% vs. 60.7%, P = 0.035), whereas 12 months' treatment induced sustained remission significantly more often only in patients with genotype 1 (6/12 vs. 0/8, P = 0.024).
In chronic hepatitis C treatment HCV genotype and serum HCV RNA after 6 months of therapy are strong predictive factors of a sustained response, and a 12-month rather than a 6-month interferon regimen may induce a more persistent clearance of HCV RNA in total and a higher sustained response rate in patients with HCV genotype 1 and in those who clear HCV RNA after 6 months of therapy.
评估以常规剂量3MU每周三次治疗6个月或12个月的α-干扰素治疗慢性丙型肝炎患者的生化和病毒学反应,并分析血清HCV RNA清除情况及HCV基因型在预测持续生化缓解中的意义。
希腊雅典西阿提卡综合医院肝病科。
60例经组织学确诊的慢性丙型肝炎患者。
所有患者接受剂量为3MU每周三次的α-2b干扰素治疗,疗程6个月(n = 26)或12个月(n = 34)。采用聚合酶链反应法对系列血清样本进行回顾性检测以确定是否存在HCV RNA,并对治疗前血清样本进行HCV基因型测定。
12个月治疗组的持续生化反应率显著更高(62%对35%,P = 0.037)。在56例治疗前可检测到HCV RNA的患者中,33例(58.9%)在治疗结束时实现了血清HCV RNA清除。治疗6个月的患者血清中HCV RNA再次出现的频率显著高于治疗12个月的患者(35.7%对5.3%,P = 0.037)。治疗6个月后的血清HCV RNA是持续生化反应的一个预后因素,HCV RNA阴性患者中有75%出现持续生化反应,而HCV RNA阳性患者中仅为16.7%(比值比0.067,P < 0.001)。此外,在治疗6个月后HCV RNA阴性的患者中,12个月治疗的持续反应率高于6个月治疗(89%对57%,P = 0.05)。HCV基因型1与显著更低的持续反应率相关(30%对60.7%,P = 0.035),而12个月治疗仅在基因型1的患者中更常诱导持续缓解(6/12对0/8,P = 0.024)。
在慢性丙型肝炎治疗中,HCV基因型及治疗6个月后的血清HCV RNA是持续反应的强预测因素,12个月而非6个月的干扰素治疗方案可能总体上诱导更持久的HCV RNA清除,并使HCV基因型1的患者及治疗6个月后清除HCV RNA的患者有更高的持续反应率。