Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea.
Clin Mol Hepatol. 2013 Mar;19(1):51-9. doi: 10.3350/cmh.2013.19.1.51. Epub 2013 Mar 25.
BACKGROUND/AIMS: The widespread use of cytotoxic chemotherapy and immunosuppressants has resulted in reactivation of hepatitis B virus (HBV) recently becoming an issue. Although rituximab (an anti-CD20 monoclonal antibody) has revolutionized the treatment of lymphoma, recent reports have suggested that rituximab therapy increases the risk of viral-mediated complications, and particularly HBV reactivation. This study analyzed real clinical practice data for rituximab-related HBV reactivation.
Between January 2005 and December 2011, 169 patients received treatment with rituximab. Screening status of the HBV infection and frequency of preemptive therapy were determined in these patients, and the clinical features of HBV reactivation were analyzed.
Seventy-nine of the 169 patients with chronic or past HBV infection were selected for evaluation of HBV reactivation. Of the 90 patients who were excluded, 22 (13.0%) were not assessed for HBsAg and anti-HBc, and 14 (8.3%) were not assessed for anti-HBc due to seronegativity for HBsAg. The selected patients were divided into those with chronic HBV infection (n=12) and those with past HBV infection (n=67); six patients (7.6%) experienced HBV reactivation. Eight patients received preemptive therapy, but three patients (37.5%) underwent HBV reactivation. Although HBsAg seropositivity was an independent risk factor for HBV reactivation (P=0.038), of the six patients with HBV reactivation, two (33.3%) had past HBV infection and three (50%) died of liver failure.
The findings of this study demonstrate that adherence to guidelines for screening and preemptive therapy for HBV reactivation was negligent among the included cohort. Attention should be paid to HBV reactivation in patients with past as well as chronic HBV infection during and after rituximab therapy.
背景/目的:细胞毒性化疗和免疫抑制剂的广泛应用导致乙型肝炎病毒(HBV)的再激活最近成为一个问题。虽然利妥昔单抗(一种抗 CD20 单克隆抗体)彻底改变了淋巴瘤的治疗方法,但最近的报告表明,利妥昔单抗治疗会增加病毒介导的并发症的风险,特别是 HBV 再激活的风险。本研究分析了利妥昔单抗相关 HBV 再激活的真实临床实践数据。
在 2005 年 1 月至 2011 年 12 月期间,169 例患者接受了利妥昔单抗治疗。对这些患者的 HBV 感染筛查状态和预防性治疗的频率进行了确定,并分析了 HBV 再激活的临床特征。
在有慢性或既往 HBV 感染的 169 例患者中,有 79 例入选评估 HBV 再激活。在排除的 90 例患者中,22 例(13.0%)未评估 HBsAg 和抗-HBc,14 例(8.3%)因 HBsAg 阴性而未评估抗-HBc。入选的患者分为慢性 HBV 感染组(n=12)和既往 HBV 感染组(n=67);有 6 例(7.6%)患者发生了 HBV 再激活。8 例患者接受了预防性治疗,但其中 3 例(37.5%)发生了 HBV 再激活。虽然 HBsAg 阳性是 HBV 再激活的独立危险因素(P=0.038),但在 6 例 HBV 再激活患者中,有 2 例(33.3%)既往有 HBV 感染,有 3 例(50%)死于肝功能衰竭。
本研究的结果表明,纳入的队列中对 HBV 再激活的筛查和预防性治疗指南的遵循存在疏忽。在利妥昔单抗治疗期间和之后,应注意慢性和既往 HBV 感染患者的 HBV 再激活。