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临床试验/NCT04942886
NCT04942886Enrolling By Invitation不适用

A Randomized, Prospective, Comparative Study of the Effectiveness of Prophylactic Entecavir Treatment for HBV Reactivation in Past HBV Infected Patients With Hematopoietic Stem Cell Transplantation

Seoul St. Mary's Hospital1 个研究点 分布在 1 个国家目标入组 226 人开始时间: 2021年8月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
226
试验地点
1
主要终点
Comparison of the rate of HBV reactivation between the treatment and delayed treatment groups.

研究概览

简要总结

This study is a randomized, prospective, comparative study of the effectiveness of prophylactic entecavir treatment for HBV reactivation in past HBV infected patients (HBsAg-, HBcIgG+) with allogeneic hematopoietic stem cell transplantation.

详细描述

This study is a randomized, prospective, comparative study of the effectiveness of prophylactic entecavir treatment for HBV reactivation in past HBV infected patients (HBsAg-, HBcIgG+) with allogeneic hematopoietic stem cell transplantation.

In this study, patients are randomized into treatment group or delayed treatment group.

* Stratified randomization (Block randomization within strata) according to the presence of HBsAb at baseline was used in this study.

  1. Experimental: Treatment group (n=113) The intervention group take entecavir 0.5mg everyday by oral administration for 3 years after allogeneic hematopoietic stem cell transplantation. The intervention group visit clinic every month and examined liver function test, HBsAg/Ab. HBV DNA level is examined at every 3 months.

* oral administration of entecavir is planned to start within 7 days after hematopoietic stem cell transplantation. 2. No Intervention: delayed treatment group (n=113) The delayed treatment group visit clinic every month and examined liver function test, HBsAg/Ab. HBV DNA level is examined at every 3 months. If the patient in the delayed treatment group shows HBV reactivation (positive HBsAg or HBV DNA ≥10 IU/mL), entecavir treatment is started.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 19 - 70
  • Patients receiving allogeneic hematopoietic stem cell transplantation
  • HBV serologic test: HBsAg (-), anti-HBc IgG (+) before receiving allogeneic hematopoietic stem cell transplantation
  • ECOG performence: 0-2
  • patients with informed consent

排除标准

  • HBV DNA (+, ≥10 IU/mL) at the time of screening
  • Receiving hematopoietic stem cell transplantation from donor with HBsAg+
  • Combined other chronic liver disease (severe alcoholics, autoimmune hepatitis, chronic hepatitis C etc.)
  • Previous antiviral therapy history for chronic hepatitis B
  • Other concomitant malignancy
  • Combined autoimmune disease (rheumatic arthritis, SLE etc)
  • CTP class B, C
  • Decompensated complications (ascites, hepatic encephalopathy etc.)
  • Active tuberculosis
  • Patients with lymphoma
  • Patients receiving autologous hematopoietic stem cell transplantation

研究组 & 干预措施

Treatment group

Experimental

The intervention group take entecavir 0.5mg everyday by oral administration for 3 years after allogeneic hematopoietic stem cell transplantation. The intervention group visit clinic every month and examined liver function test, HBsAg/Ab. HBV DNA level is examined at every 3 months.

干预措施: Baracle Tab.® (Drug)

结局指标

主要结局

Comparison of the rate of HBV reactivation between the treatment and delayed treatment groups.

时间窗: The primary outcome is evaluated during 3 years after hematopoietic stem cell transplantation

Comparing the rate of HBV reactivation between the treatment and delayed treatment groups during 3 years after hematopoietic stem cell transplantation \* Definition of HBV reactivation: HBsAg ≥ 1.0 S/CO or HBV DNA ≥ 10 IU/mL

次要结局

  • Comparison of the rate of active hepatitis with HBV reactivation between the treatment and delayed treatment groups.(The secondary outcomes are evaluated during 3 years after hematopoietic stem cell transplantation.)
  • Comparison of the rate of survival related to HBV reactivation between the treatment and delayed treatment groups.(The secondary outcomes are evaluated during 3 years after hematopoietic stem cell transplantation.)
  • Comparison of the rate of hepatic failure related to HBV reactivation between the treatment and delayed treatment groups.(The secondary outcomes are evaluated during 3 years after hematopoietic stem cell transplantation.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dong-Gun Lee

professor

Seoul St. Mary's Hospital

研究点 (1)

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