| Literature DB >> 27358178 |
Yutaka Tsukune1, Makoto Sasaki2, Takeshi Odajima3, Atsushi Isoda4, Morio Matsumoto4, Michiaki Koike5, Hideto Tamura6, Keiichi Moriya6, Shigeki Ito7, Maki Asahi8, Yoichi Imai9, Junji Tanaka9, Hiroshi Handa10, Hiromi Koiso11, Sakae Tanosaki12, Jian Hua13, Masao Hagihara13, Yuriko Yahata1, Satoko Suzuki14, Sumio Watanabe15, Hiroki Sugimori16, Norio Komatsu1.
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.Entities:
Keywords: Hepatitis B; Multiple myeloma; Novel agents; Viral reactivation
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Year: 2016 PMID: 27358178 DOI: 10.1007/s00277-016-2742-7
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673