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标题: EASL2019 THU-214 FIB-4指数的年平均值与HBV核心相关 抗原作为启动 [打印本页]

作者: StephenW    时间: 2019-4-4 13:04     标题: EASL2019 THU-214 FIB-4指数的年平均值与HBV核心相关 抗原作为启动

THU-214
Annual average of integral FIB-4 index and HBV core-related
Antigen as an appropriate indicators for starting nucleoside
Analogs at an optimum timing
Shuhei Hige1, Itaru Ozeki1, Hirokazu Suii1, Ryoji Tatsumi1,
Masakatsu Yamaguchi1, Mutsuumi Kimura1, Tomohiro Arakawa1,
Tomoaki Nakajima1, Yasuaki Kuwata1, Takumi Ohmura1, Joji Toyota1,
Yoshiyasu Karino1. 1Sapporo-Kosei General Hospital, Hepatology,
Sapporo,
Email: [email protected]
Background and aims: Although nucleos (t)ide analogue (NA) has
Reported to be useful for suppressing hepatocellular carcinoma
(HCC) with hepatitis B patients, it is important not to miss an
Optimum timing of starting NA because not a few patients progress to
HCC later. Serum HBV core-related antigen (HBcrAg) is reported
To correlate with intrahepatic cccDNA which may be related to viral
Activity and carcinogenic risk. In this study,
Average of integral FIB-4 index (aaFIB-4) and serum HBcrAg for
Determine an adequate timing of NA and estimating the HCC risk
During NA treatment.
Method: A total of 522 HBs antigen (HBsAg)-positive patients who
Did not have a history of HCC were followed from the start of NA
[entecavir (ETV) 319, lamivudine (Lam) to ETV 76, Lam 28, Lam or ETV
Plus adefovir (ADV) 99 cases]. An aaFIB-4 was calculated from
The integral value of each FIB-4 index during the same year. Serum
Levels of HBcrAg were measured by the LumipulseR HBcrAg Chemiluminescence Enzyme Immunoassay (Fujirebio, Tokyo, Japan).
The dynamic range of the assay is 3.0 to 6.8 (log10 U/ml). Kaplan-
Meier method was used to estimate the cumulative occurrence of
HCC.
Results: During the median follow-up of 107 months, HCC was
Confirmed in 79 patients. Overall cumulative 5/10 year occurrence
Rate of HCC (5/10y-HCC rate) was 10.0/18.2%. The cut off value of
aaFIB-4 and log10 HBsAg at the start of NA treatment for the
Occurrence of HCC during the treatment course was 3.00 and 3.2
(log10 IU/ml) by ROC analysis. 5y-HCC rate was 0/2.3/1.1/18.7/31.3 (%)
For those whose pretreatment aaFIB-4 was <1.0/1.0-2.0/2.0-3.0/3.0-
4.0/4.0 ≤ and 5.1/15.9/5.7 (%) for those whose pretreatment HBcrAg
Was <3.0/3.0-6.8/6.8 < .5/10y-HCC rate by the combined conditions is
Shown in Table. High aaFIB-4 was a significant predictive factor of
HCC and high HBsAg/low HBcrAg indicated low risk of HCC.
Of high aaFIB-4/low HBsAg, probability of HCC increased with
Increasing HBcrAg. 10y-HCC rate of cases↻ HBcrAg residual
<3.0 (Gr.1), decreased to <3.0 (Gr.2), remained ≥3.0 (Gr.3) was 5.1/
11.9/17.8 (%). Among high aa FIB-4 cases, 5y-HCC risk of those whose
Aa FIB-4 declined below3.00 during NA treatment was 17.2%,
Those who did not showaaFIB-4 decrease was 29.5% (p = 0.04).
Table: 5y/10y-HCC rate (%) by the combined conditions of aaFIB-4
Index, HBcrAg and HBsAg.
Overall     aaFIB-4 <3.00    aaFIB-4 ≥3.00
log10HBsAg   <3.2 3.2 ≤   ,  <3.2 3.2 ≤  , <3.2 3.2 ≤
HBcrAg <3.0 8.4/8.4 2.3/2.3   ,  0/0 0/0   ,19.0/19.0 0/0
           3.0–6.8 17.6/30.2 11.9/19.6  ,5.0/14.7 2.4/5.1    ,  22.9/48.0 24.6/39.2
           6.8 < 10.3/17.6 1.4/8.6 0/0   ,0/3.5 27.3/62.7     ,17.6/21.6
Conclusion: AaFIB-4 and HBcrAg at the start of NA treatment was
Corroded with occurrence of HCC afterwards. NA should be started
Before aaFIB-4 index reaches 3.00. The decrease of aaFIB-4 or HBcrAg
After NA treatment may reduce the risk of HCC.
Conclusion: AaFIB-4 and HBcrAg at the start of NA treatment was
Corroded with occurrence of HCC afterwards. NA should be started
Before aaFIB-4 index reaches 3.00. The decrease of aaFIB-4 or HBcrAg
After NA treatment may reduce the risk of HCC.
作者: StephenW    时间: 2019-4-4 13:05

THU-214
FIB-4指数的年平均值与HBV核心相关
抗原作为启动核苷的适当指标
模拟在最佳时机
Shuhei Hige1,Itaru Ozeki1,Hirokazu Suii1,Ryoji Tatsumi1,
Masakatsu Yamaguchi1,Mutsuumi Kimura1,Tomohiro Arakawa1,
Tomoaki Nakajima1,Yasuaki Kuwata1,Takumi Ohmura1,Joji Toyota1,
Yoshiyasu Karino1。 1Sapporo-Kosei综合医院,肝脏病学,
札幌,
电子邮件:[email protected]
背景和目的:虽然核苷(t)ide类似物(NA)具有
据报道可用于抑制肝细胞癌
(HCC)乙型肝炎患者,重要的是不要错过
起始NA的最佳时机,因为没有一些患者进展
HCC后来。报道了血清HBV核心相关抗原(HBcrAg)
与可能与病毒相关的肝内cccDNA相关
活动和致癌风险。在这个研究中,
整体FIB-4指数(aaFIB-4)和血清HBcrAg的平均值
确定NA的适当时间并估计HCC风险
NA治疗期间。
方法:共有522名HBs抗原(HBsAg)阳性患者
从NA开始就没有HCC史
[恩替卡韦(ETV)319,拉米夫定(Lam)至ETV 76,Lam 28,Lam或ETV
加阿德福韦(ADV)99例]。 aaFIB-4计算自
同年每个FIB-4指数的积分值。血清
通过LumipulseR HBcrAg化学发光酶免疫测定法(Fujirebio,Tokyo,Japan)测量HBcrAg的水平。
测定的动态范围是3.0至6.8(log10U / ml)。卡普兰
Meier方法用于估计累积的发生率
HCC。
结果:在107个月的中位随访期间,HCC为
确诊79例患者。总累计5/10年发生
HCC率(5 / 10y-HCC率)为10.0 / 18.2%。截止值
aaFIB-4和log10 HBsAg在NA治疗开始时为
治疗过程中HCC的发生率为3.00和3.2
(log10IU / ml)通过ROC分析。 5y-HCC率为0 / 2.3 / 1.1 / 18.7 / 31.3(%)
对于预处理aaFIB-4 <1.0 / 1.0-2.0 / 2.0-3.0 / 3.0-的人
对于预处理HBcrAg的人,4.0 /4.0≤和5.1 / 15.9 / 5.7(%)
组合条件下<3.0 / 3.0-6.8 / 6.8 <.5 / 10y-HCC率
如表所示。高aaFIB-4是一个重要的预测因子
HCC和高HBsAg /低HBcrAg表明HCC风险低。
高aaFIB-4 /低HBsAg,HCC的概率随着增加而增加
增加HBcrAg。 10-HCC病例率为HBcrAg残留
<3.0(Gr.1),降至<3.0(Gr.2),保持≥3.0(Gr.3)为5.1 /
11.9 / 17.8(%)。在高aa FIB-4病例中,5y-HCC的风险是那些
在NA治疗期间,Aa FIB-4下降至3.00以下,为17.2%,
那些没有表现出FIB-4减少的人是29.5%(p = 0.04)。
表:aaFIB-4的组合条件下的5y / 10y-HCC速率(%)
指数,HBcrAg和HBsAg。
总体而言aaFIB-4 <3.00 aaFIB-4≥3.00
log10HBsAg <3.23.2≤<3.23.2≤<3.23.2≤
HBcrAg <3.0 8.4 / 8.4 2.3 / 2.3 0/0 0/0 19.0 / 19.0 0/0
3.0-6.8 17.6 / 30.2 11.9 / 19.6 5.0 / 14.7 2.4 / 5.1 22.9 / 48.0 24.6 / 39.2
6.8 <10.3 / 17.6 1.4 / 8.6 0/0 0 / 3.5 27.3 / 62.7 17.6 / 21.6
结论:NA治疗开始时AaFIB-4和HBcrAg为
随后发生HCC腐蚀。 NA应该开始
在aaFIB-4指数达到3.00之前。 aaFIB-4或HBcrAg的减少
NA治疗后可降低HCC的风险。




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