Poo Jorge Luis, Sánchez-Avila F, Kershenobich D, García-Samper X, Gongora J, Uribe M
Centro de Investigacion Farmacológica y Biotecnológica, Medica Sur Hospital and Clinical Foundation, Mexico City, Mexico.
J Gastroenterol Hepatol. 2004 Dec;19 Suppl 6:S79-81. doi: 10.1111/j.1440-1746.2004.03634.x.
Despite steady progress in antiviral treatment for patients with chronic hepatitis C virus (HCV), many patients still have detectable serum HCV RNA levels by the end of interferon-based treatment and are known as virological non-responders. Re-treatment of these patients not responding to previous therapy remains challenging. Studies of the dynamics of the HCV population show a marked decline in new cases since 1996; however, the relative proportion of non-responders is expected to increase over time and, similarly, the number of patients eligible for first-line treatment is expected to decrease. The current standard of care for treatment involves the use of pegylated interferons in combination with ribavirin. However, many difficult-to-treat groups still have low response rates. Newer combinations are being investigated to optimize chances of attaining a sustained response in these groups: one such triple therapy regimen is peginterferon alfa-2a, ribavirin and thymalfasin, which was given to 23 previously non-responder patients. Viral response was 60.8% at week 12 and 47.8% at week 24. These preliminary results encourage further evaluation of this promising combination.
尽管慢性丙型肝炎病毒(HCV)患者的抗病毒治疗取得了稳步进展,但许多患者在基于干扰素的治疗结束时血清HCV RNA水平仍可检测到,这些患者被称为病毒学无应答者。对这些对先前治疗无反应的患者进行再治疗仍然具有挑战性。HCV群体动态研究表明,自1996年以来新病例显著减少;然而,预计无应答者的相对比例会随着时间的推移而增加,同样,符合一线治疗条件的患者数量预计会减少。目前的治疗护理标准包括使用聚乙二醇化干扰素联合利巴韦林。然而,许多难治性群体的应答率仍然很低。正在研究更新的联合治疗方案,以优化这些群体获得持续应答的机会:一种这样的三联疗法方案是聚乙二醇化干扰素α-2a、利巴韦林和胸腺法新,该方案应用于23名先前的无应答患者。第12周时病毒应答率为60.8%,第24周时为47.8%。这些初步结果鼓励对这种有前景的联合治疗方案进行进一步评估。