首页> 外文期刊>Expert opinion on pharmacotherapy >Lamivudine for the prevention of hepatitis B virus reactivation after high-dose chemotherapy and autologous hematopoietic stem cell transplantation for patients with advanced or relapsed non-Hodgkin's lymphoma single institution experience.
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Lamivudine for the prevention of hepatitis B virus reactivation after high-dose chemotherapy and autologous hematopoietic stem cell transplantation for patients with advanced or relapsed non-Hodgkin's lymphoma single institution experience.

机译:拉米夫定预防晚期或复发性非霍奇金淋巴瘤患者接受大剂量化疗和自体造血干细胞移植后乙型肝炎病毒再激活的单一机构经验。

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OBJECTIVE: Hepatitis B virus (HBV) reactivation is a well-known complication in cancer patients receiving cytotoxic chemotherapy, resulting in varying degrees of liver damage. The objective of this study was to investigate the efficacy of lamivudine for the prevention of HBV reactivation in non-Hodgkin's lymphoma (NHL) patients undergoing high-dose chemotherapy and autologous hematopoietic stem cell transplantation (AHSCT). RESEARCH DESIGN AND METHODS: Thirty-two patients with NHL who were HBV surface antigen (HBsAg)-positive were enrolled in this pilot study. They were divided into two groups: 20 patients received prophylactic oral lamivudine 100 mg/day before, and until at least 6 months after transplantation. The historical control group comprised 12 patients who received high-dose chemotherapy and AHSCT without lamivudine. The incidence and severity of hepatitis due to HBV reactivation, as well as other adverse clinical outcomes, were compared between the two groups. RESULTS: Most baseline clinical characteristics were similar in the two groups, except for HBV e-antigen (HBeAg)-positive status (85% in the lamivudine group vs 33.3% in the control group, p = 0.006) and the type of AHSCT. There was a lower incidence of hepatitis due to HBV reactivation in the lamivudine group than in the control group (10 vs 50%, p = 0.030), less severe hepatitis (0 vs 25%, p = 0.009), and lower mortality (0 vs 25%, p = 0.236). An HBV variant with tyrosine methionine aspartate aspartate (YMDD) mutation was detected in one patient in the lamivudine group (5%) after administration of lamivudine for 9 months. No significant adverse events were associated with the use of prophylactic lamivudine, and hematopoietic reconstitution was not affected by the intervention. CONCLUSIONS: Prophylactic lamivudine may reduce the incidence and severity of chemotherapy-related HBV reactivation and hepatitis-related mortality in HBsAg-positive NHL patients receiving high-dose chemotherapy and AHSCT. Additional randomized, multicenter trials are warranted.
机译:目的:乙型肝炎病毒(HBV)的重新激活是接受细胞毒性化学疗法的癌症患者的众所周知的并发症,导致不同程度的肝损伤。这项研究的目的是研究拉米夫定在接受大剂量化疗和自体造血干细胞移植(AHSCT)的非霍奇金淋巴瘤(NHL)患者中预防HBV激活的功效。研究设计和方法:32例HBV表面抗原(HBsAg)阳性的NHL患者入选了该试验研究。他们分为两组:20例患者在移植前100毫克/天和至少移植后6个月接受口服拉米夫定预防性治疗。历史对照组包括12例接受大剂量化疗和AHSCT且未使用拉米夫定的患者。在两组之间比较了由HBV激活引起的肝炎的发生率和严重程度,以及其他不良的临床结果。结果:除HBV e-抗原(HBeAg)呈阳性状态(拉米夫定组为85%,对照组为33.3%,p = 0.006)和AHSCT类型外,两组的大多数基线临床特征相似。拉米夫定组的HBV激活引起的肝炎发生率比对照组低(10 vs 50%,p = 0.030),轻度肝炎(0 vs 25%,p = 0.009)和较低的死亡率(0 vs 25%,p = 0.236)。拉米夫定组治疗9个月后,在拉米夫定组(5%)的一名患者中检测到酪氨酸甲硫氨酸天冬氨酸(YMDD)突变的HBV变异。预防性拉米夫定的使用无重大不良事件发生,且干预措施未影响造血重建。结论:预防性拉米夫定可降低接受大剂量化疗和AHSCT的HBsAg阳性NHL患者化疗相关的HBV激活的发生率和严重程度,并降低与肝炎相关的死亡率。需要进行其他随机,多中心试验。

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