Health Services Research and Development Center of Excellence, VA Puget Sound Healthcare System, Seattle, Washington, USA.
Clin Gastroenterol Hepatol. 2010 Nov;8(11):972-8. doi: 10.1016/j.cgh.2010.07.012. Epub 2010 Aug 6.
BACKGROUND & AIMS: A significant proportion of patients with hepatitis C virus (HCV) infection discontinue antiviral treatment prematurely. Risk factors for discontinuation before 48 weeks among patients with genotype 1 HCV vary over the course of therapy. We investigated the rates and risk factors for treatment discontinuation within 12 weeks, 12-24 weeks, and 24-48 weeks.
We retrospectively evaluated data from all Veterans Affairs (VA) patients with genotype 1 HCV who initiated pegylated interferon and ribavirin therapy from 2002-2007 (n = 11,019). We accounted for appropriate discontinuation because of viral nonresponse.
Overall, 53% of patients completed at least 38.4 weeks of therapy (80% of the projected 48 weeks), 16.5% discontinued early in the setting of viral nonresponse, and 30.9% discontinued despite viral response or in the absence of virologic data. Cirrhosis, diabetes, pretreatment substance use disorder, hemoglobin, and lack of hematopoietic growth factor use independently predicted discontinuation before 12 weeks (P < .05 for all). Among patients with documented early virologic responses, higher baseline levels of creatinine, depression, and lack of growth factor use predicted discontinuation from 12-24 weeks. No factors independently predicted discontinuation from 24-48 weeks among patients responding to treatment at 24 weeks.
Early discontinuation of antiviral therapy is common. Use of growth factors was the strongest independent predictor of treatment retention before 24 weeks and should be evaluated prospectively. Early interventions may also be warranted for other risk factors for early discontinuation, such as pre-existing substance use, depression, cirrhosis, or diabetes.
相当比例的丙型肝炎病毒(HCV)感染患者会提前终止抗病毒治疗。在治疗过程中,基因型 1 HCV 患者在 48 周前停药的风险因素各不相同。我们调查了在 12 周、12-24 周和 24-48 周内停药的发生率和风险因素。
我们回顾性评估了 2002-2007 年期间所有开始接受聚乙二醇干扰素和利巴韦林治疗的基因型 1 HCV 退伍军人事务部(VA)患者的数据(n=11019)。我们考虑了因病毒无应答而适当停药的情况。
总体而言,53%的患者完成了至少 38.4 周的治疗(80%的预期 48 周),16.5%因病毒无应答而提前停药,30.9%尽管病毒应答或缺乏病毒学数据仍停药。肝硬化、糖尿病、治疗前物质使用障碍、血红蛋白和未使用造血生长因子独立预测了 12 周内停药(所有 P<0.05)。在有早期病毒学应答记录的患者中,基线肌酐、抑郁和缺乏生长因子使用水平较高预测了从 12-24 周的停药。在 24 周时对治疗有应答的患者中,没有任何因素独立预测从 24-48 周的停药。
抗病毒治疗的早期停药很常见。生长因子的使用是治疗前保留治疗的最强独立预测因素,应进行前瞻性评估。对于其他早期停药的风险因素,如预先存在的物质使用、抑郁、肝硬化或糖尿病,也可能需要早期干预。