von Wagner Michael, Huber Miriam, Berg Thomas, Hinrichsen Holger, Rasenack Jens, Heintges Tobias, Bergk Alexandra, Bernsmeier Christine, Häussinger Dieter, Herrmann Eva, Zeuzem Stefan
Universitätsklinikum des Saarlandes, Homburg/Saar, Germany.
Gastroenterology. 2005 Aug;129(2):522-7. doi: 10.1016/j.gastro.2005.05.008.
BACKGROUND & AIMS: Standard therapy of patients with chronic hepatitis C virus (HCV) infected with HCV genotype-2 or -3 is the combination of pegylated interferon-alpha and ribavirin for 24 weeks. Whether shorter treatment durations are possible for these patients without compromising sustained virologic response rates is unknown.
Patients chronically infected with HCV-2 (n = 39), HCV-2/3 (n = 1), or HCV-3 (n = 113) were treated with peginterferon-alpha-2a (180 microg/wk) plus ribavirin 800-1200 mg/day. HCV RNA was quantitatively assessed after 4 weeks. Patients with a rapid virologic response (HCV RNA below 600 IU/mL) were randomized for a total treatment duration of 16 (group A) or 24 weeks (group B). All patients with HCV RNA > or =600 IU/mL at week 4 (group C) were treated for 24 weeks. End-of-treatment and sustained virologic response were assessed by qualitative RT-PCR (sensitivity 50 IU/mL).
Only 11 of 153 patients (7%) were allocated to group C. End-of-treatment and sustained virologic response rates were 94% and 82%, (group A), 85% and 80% (group B), and 73% and 36% (group C), respectively. In patients infected with genotype HCV-3 and high viral load (>800,000 IU/mL), a significant lower sustained virologic response rate was found than in patients infected with HCV-3 and a viral load lower or equal to 800,000 IU/mL (59% vs 85%, respectively; P = .003).
In HCV-2 and -3 (low viral load)-infected patients who have a rapid virologic response, treatment for 16 weeks with peginterferon-alpha-2a and ribavirin is sufficient. In patients infected by HCV-3 (high viral load), longer treatment may be necessary.
慢性丙型肝炎病毒(HCV)2型或3型感染患者的标准治疗方案是聚乙二醇化干扰素-α与利巴韦林联合使用24周。对于这些患者,在不影响持续病毒学应答率的情况下缩短治疗疗程是否可行尚不清楚。
对慢性感染HCV-2(n = 39)、HCV-2/3(n = 1)或HCV-3(n = 113)的患者,采用聚乙二醇化干扰素-α-2a(180μg/周)加利巴韦林800 - 1200mg/天进行治疗。4周后对HCV RNA进行定量评估。具有快速病毒学应答(HCV RNA低于600IU/mL)的患者被随机分为总治疗疗程为16周(A组)或24周(B组)。所有在第4周时HCV RNA≥600IU/mL的患者(C组)接受24周治疗。通过定性逆转录聚合酶链反应(灵敏度50IU/mL)评估治疗结束时和持续病毒学应答情况。
153例患者中仅有11例(7%)被分配至C组。治疗结束时和持续病毒学应答率分别为:A组94%和82%,B组85%和80%,C组73%和36%。在感染HCV-3且病毒载量高(>800,000IU/mL)的患者中,发现持续病毒学应答率显著低于感染HCV-3且病毒载量低于或等于800,000IU/mL的患者(分别为59%对85%;P = 0.003)。
在HCV-2和HCV-3(低病毒载量)感染且具有快速病毒学应答的患者中,使用聚乙二醇化干扰素-α-2a和利巴韦林治疗16周就足够了。对于HCV-3(高病毒载量)感染的患者,可能需要更长时间的治疗。