摘要
目的聚乙二醇干扰素(Peg—IFN)α-2a联合利巴韦林治疗1b型慢性丙型病毒性肝炎患者,延长疗程至72周与标准治疗的48周疗程比较,是否获得更高的持续病毒学应答率(SVR)。方法113例基因型1b慢性丙型病毒性肝炎患者经知情同意分为两组,A组(疗程48周)37例,B组(疗程72周)76例,分别给予Peg—IFNα-2a联合利巴韦林抗病毒治疗,治疗结束后随访24周。分别于治疗第4、12周,治疗结束时和结束后24周检测丙型肝炎病毒(HCV)RNA。结果分析采用按意向性治疗原则(ITT)方法。结果A组与B组快速病毒学应答率(RVR)分别为78.38%(29/37)、80.26%(61/76),差异无统计学意义(P〉0.05);早期病毒学应答率(EVR)分别为83.78%(31/37)、85.53%(65/76),差异无统计学意义(P〉0.05);治疗结束时病毒学应答率(ETVR)分别为91.89%(34/37)、90.79%(69,/76),差异无统计学意义(P〉0.05);SVR分别是64.86%(24/37)、84.21%(64/76),差异有统计学意义(P〈0.05)。A组与B组中取得RVR患者的SVR分别是75.86%(22/29)、95.08%(58/61),差异有统计学意义(P〈0.05)。结论对于基因型1b的丙型病毒性肝炎患者,采用Peg—IFNα-2a联合利巴韦林抗病毒治疗,不论是否取得RVR,将疗程延长至72周与标准治疗的48周比较获得更高的SVR。
Objective -To investigate whetherextension treatment of 72 weeks by using peginter- feron (Peg -IFN)α -2a plus ribavirin (RBV) for type 1 b chronic hepatitis C patients could acquire high- er sustained virologic response (SVR) rate than traditional treatment of 48 weeks or not. Methods 113 patients with genotype type 1 b chronic hepatitis C were divided into group A (48 weeks, n = 37) and group B (72 weeks,n =76) by informed consent with the treatment of Peg - IFNα- 2a plus ribavirin. All the pa- tients were followed - up for 24 weeks after the end of treatment. Hepatitis C virus (HCV) RNA was re- spectively detected at 4th week, and 12th week during the treatment, the end of treatment and 24 weeks af- ter the treatment. Outcomes analysis was conducted according to intention - to - treat principles. Results There was no statistically significant difference between group A and group B in rapid virologic response (RVR) rate (78. 38% vs. 80. 26% ), early virologic response (EVR) rate (83.78% vs. 85.53% ) and end - of - treatment virologic response (ETVR) rate (91.89 % vs. 90.79 ) ( P 〉 0. 05). But the SVR rate in group B ( 84. 21%, 64/76) was higher than in group A (64. 86%, 24/37 ) ( P 〈 0. 05 ). The SVR rate in achieving RVR patients of group B (95.08%, 58/61) was also higher than in group A (75.86%, 22/29, P 〈 0. 05 ). Conclusion Extension of treatment with Peg - IFNα - 2a plus ribavirin from 48 weeks to 72 weeks could increase the rate of SVR in patients who achieved RVR or not.
出处
《中华实验外科杂志》
CAS
CSCD
北大核心
2016年第3期768-770,共3页
Chinese Journal of Experimental Surgery
基金
国家自然科学基金(U1404309)