在血液恶性肿瘤化疗期间接受预防性拉米夫定治疗的无症状乙型肝炎病毒携带者中乙型肝炎病毒突变的频率

Anna Maria Pelizzari, Maddalena Motta, Elisabetta Cariani, Paola Turconi, Erika Borlenghi, Giuseppe Rossi
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引用次数: 29

摘要

乙型肝炎病毒(HBV)再激活是无症状HBV携带者化疗的潜在致命并发症。预防性拉米夫定已被证明对其预防有效,但慢性肝炎治疗患者中可能出现拉米夫定耐药HBV YMMD突变体,这可能限制其使用。为了评估HBV YMMD突变的频率及其临床意义,我们分析了32个疗程的血液恶性肿瘤HBV携带者从化疗开始到化疗结束后1-5个月的拉米夫定预防。拉米夫定的中位使用时间为6个月(范围2-24+),中位随访时间为19.5个月(范围5-40)。化疗结束后和拉米夫定停药后,轻度肝炎的HBV再激活发作4次,没有突变株的证据。在随访中,1例连续使用拉米夫定20个月的转氨酶水平正常的患者检测到YMMD突变体。总之,在接受血液学恶性肿瘤化疗的HBV携带者中,在预防性拉米夫定疗程中出现HBV YMMD突变的发生率为3.1%,与临床相关性很小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Frequency of hepatitis B virus mutant in asymptomatic hepatitis B virus carriers receiving prophylactic lamivudine during chemotherapy for hematologic malignancies.

Hepatitis B virus (HBV) reactivation is a potentially fatal complication of chemotherapy in asymptomatic HBV carriers. Prophylactic lamivudine has proven effective for its prevention, but the potential emergence of lamivudine-resistant HBV YMMD mutants, as shown in patients treated for chronic hepatitis, may limit its use. To evaluate the frequency of HBV YMMD mutant and its clinical significance, we have analysed 32 courses of primary lamivudine prophylaxis given to HBV carriers with haematologic malignancies, from the start until 1-5 months after the end of chemotherapy. Lamivudine was used for a median of 6 months (range 2-24+) and median follow-up was 19.5 months (range 5-40). Four episodes of HBV reactivation with mild hepatitis and no evidence of mutant strain occurred after chemotherapy completion and after lamivudine withdrawal. At follow-up YMMD mutant was detected in one patient with normal transaminase levels, who had been on continuous lamivudine for 20 months. In conclusion, among HBV carriers treated with chemotherapy for haematologic malignancies, the emergence of HBV YMMD mutant occurred in 3.1% of prophylactic lamivudine courses and was of little clinical relevance.

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