Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Hepatol. 2012 Dec;57(6):1177-85. doi: 10.1016/j.jhep.2012.07.031. Epub 2012 Aug 4.
BACKGROUND & AIMS: Data on acute exacerbation and reactivation of chronic hepatitis C virus (HCV) infection following chemotherapy are very limited. We sought to characterize the episodes of acute exacerbation and viral reactivation of HCV infection in cancer patients.
The medical records of HCV-infected patients seen at our institution (2008-2009) were analyzed retrospectively. Acute exacerbation was defined as greater than 3-fold increase in serum level of alanine aminotransferase, and viral reactivation as ≥ 1 log(10) IU/ml increase of HCV viral load following chemotherapy.
Acute exacerbation occurred in 33 (11%) of 308 patients with proven HCV infection. Patients with acute exacerbation more often had underlying hematological malignancies (73% vs. 29%; p<0.001) and lymphopenia (6% vs. 0%; p=0.01) than patients without it. In multivariate analysis, underlying hematological malignancies (p=0.02; odds ratio, 3.2; 95% confidence interval, 1.2-8.7) and use of rituximab (p=0.004; odds ratio, 4.2; 95% confidence interval, 1.6-10.9) were associated with acute exacerbation. Patients with acute exacerbation received higher median cumulative dose of rituximab than those without exacerbation. Discontinuation of chemotherapy due to liver dysfunction was more common in patients with acute exacerbation than in patients without it (45% vs. 11%; p<0.001). Eight (36%) of 22 patients with known pre- and post-chemotherapy viral load had viral reactivation.
Acute exacerbation and reactivation of chronic HCV infection occur often after chemotherapy. Liver dysfunction can lead to discontinuation of potentially life-saving chemotherapy in nearly one-half of the patients with exacerbation of HCV infection.
有关化疗后慢性丙型肝炎病毒(HCV)感染急性加重和再激活的数据非常有限。我们旨在描述癌症患者中 HCV 感染急性加重和病毒再激活的发作情况。
回顾性分析了我院(2008-2009 年)就诊的 HCV 感染患者的病历。血清丙氨酸氨基转移酶水平升高 3 倍以上定义为急性加重,化疗后 HCV 病毒载量增加≥1log10IU/ml 定义为病毒再激活。
308 例确诊 HCV 感染患者中,有 33 例(11%)发生急性加重。与未发生急性加重的患者相比,发生急性加重的患者更常患有基础血液系统恶性肿瘤(73%比 29%;p<0.001)和淋巴细胞减少症(6%比 0%;p=0.01)。多变量分析显示,基础血液系统恶性肿瘤(p=0.02;比值比,3.2;95%置信区间,1.2-8.7)和利妥昔单抗的使用(p=0.004;比值比,4.2;95%置信区间,1.6-10.9)与急性加重有关。发生急性加重的患者接受的利妥昔单抗累积中位剂量高于未发生急性加重的患者。与未发生急性加重的患者相比,因肝功能障碍而停止化疗的患者更为常见(45%比 11%;p<0.001)。22 例已知化疗前后病毒载量的患者中,有 8 例(36%)发生病毒再激活。
化疗后常发生慢性 HCV 感染的急性加重和再激活。肝功能障碍可导致近一半 HCV 感染急性加重患者停止潜在的救命化疗。