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新型药物时代多发性骨髓瘤中乙型肝炎病毒再激活的发生率及临床背景

Incidence and clinical background of hepatitis B virus reactivation in multiple myeloma in novel agents' era.

作者信息

Tsukune Yutaka, Sasaki Makoto, Odajima Takeshi, Isoda Atsushi, Matsumoto Morio, Koike Michiaki, Tamura Hideto, Moriya Keiichi, Ito Shigeki, Asahi Maki, Imai Yoichi, Tanaka Junji, Handa Hiroshi, Koiso Hiromi, Tanosaki Sakae, Hua Jian, Hagihara Masao, Yahata Yuriko, Suzuki Satoko, Watanabe Sumio, Sugimori Hiroki, Komatsu Norio

机构信息

Department of Hematology, Juntendo University School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

Faculty of Health Science, Daito Bunka University School of Sports and Health Science, Saitama, Japan.

出版信息

Ann Hematol. 2016 Sep;95(9):1465-72. doi: 10.1007/s00277-016-2742-7. Epub 2016 Jun 30.

Abstract

There are some reports regarding hepatitis B virus (HBV) reactivation in patients with myeloma who are HBV carriers or who have had a resolved HBV infection, and there is no standard prophylaxis strategy for these patients. We performed a retrospective multicenter study to determine the incidence and characteristics of HBV reactivation in patients with multiple myeloma. We identified 641 patients with multiple myeloma who had been treated using novel agents and/or autologous stem cell transplantation with high-dose chemotherapy between January 2006 and June 2014 at nine Japanese hospitals. The patients' characteristics, laboratory data, and clinical courses were retrieved and statistically analyzed. During a median follow-up of 101 weeks, one of eight (12.5 %) HBV carriers developed hepatitis and 9 of 99 (9.1 %) patients with resolved HBV infection experienced HBV reactivation; the cumulative incidences of HBV reactivation at 2 years (104 weeks) and 5 years (260 weeks) were 8 and 14 %, respectively. The nine cases of reactivation after resolved HBV infection had received entecavir as preemptive therapy or were carefully observed by monitoring their HBV DNA levels, and none of these cases developed hepatitis. Among patients with multiple myeloma, HBV reactivation was not rare. Therefore, long-term monitoring of HBV DNA levels is needed to prevent hepatitis that is related to HBV reactivation in these patients.

摘要

有一些关于骨髓瘤患者中乙型肝炎病毒(HBV)再激活的报道,这些患者为HBV携带者或曾有过HBV感染已康复者,且针对这些患者尚无标准的预防策略。我们进行了一项回顾性多中心研究,以确定多发性骨髓瘤患者中HBV再激活的发生率及特征。我们纳入了2006年1月至2014年6月期间在日本9家医院接受新型药物和/或大剂量化疗联合自体干细胞移植治疗的641例多发性骨髓瘤患者。收集了患者的特征、实验室数据及临床病程并进行统计学分析。在中位随访101周期间,8例HBV携带者中有1例(12.5%)发生肝炎,99例曾有HBV感染已康复的患者中有9例(9.1%)出现HBV再激活;2年(104周)和5年(260周)时HBV再激活的累积发生率分别为8%和14%。9例曾有HBV感染已康复后发生再激活的患者接受了恩替卡韦作为抢先治疗或通过监测其HBV DNA水平进行密切观察,这些病例均未发生肝炎。在多发性骨髓瘤患者中,HBV再激活并不罕见。因此,需要对这些患者长期监测HBV DNA水平,以预防与HBV再激活相关的肝炎。

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