aMAP评分在酒精相关性肝硬化患者队列中预测肝细胞癌发展的有效性

Ken Liu, Terry C. F. Yip, Steven Masson, Waleed Fateen, Tae-Hwi Schwantes-An, Geoffrey W. McCaughan, Timothy R. Morgan, Guruprasad P. Aithal, Devanshi Seth
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引用次数: 3

摘要

背景和目的最近设计了aMAP评分来预测肝细胞癌(HCC)的发展。然而,其在酒精相关性肝硬化(ALC)中的表现未被测试。我们的目的是在一组ALC患者中验证aMAP评分。方法纳入先前全基因组关联研究中ALC的研究参与者。所有参与者都有大量饮酒的历史。通过纤维扫描和/或组织学诊断肝硬化。随访患者至最后一次肝脏影像学检查、HCC、肝移植(LT)或死亡,后两者调整为竞争风险。结果共纳入269例ALC患者:男性(72.5%),高加索(98.9%),中位年龄56岁,Child-Pugh评分中位7分。aMAP评分中位数为60:低危12.3%,中危35.3%,高危52.4%。中位随访41个月后,14例患者发生HCC, 27例接受肝移植,104例死亡。aMAP评分预测HCC发展(风险比每增加1分1.12,P <.001),风险组间累积发生率函数分离良好。预测HCC发展的时间依赖性受试者工作特征曲线下面积在1年和5年分别为0.83和0.82,与address -HCC和退伍军人事务医疗保健系统评分相似。我们验证了aMAP评分在ALC中的优异表现,并确认了其在更广泛的病因中的适用性。
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Validation of the aMAP score to predict hepatocellular carcinoma development in a cohort of alcohol-related cirrhosis patients

Background and Aims

The aMAP score was recently devised to predict hepatocellular carcinoma (HCC) development. However, its performance was not tested in alcohol-related cirrhosis (ALC). We aimed to validate the aMAP score in a cohort of ALC patients.

Method

Study participants with ALC from a prior genome-wide association study were included. All participants had a history of high alcohol consumption. Cirrhosis was defined clinically, using fibroscan and/or histology. Patients were followed until the last liver imaging, HCC, liver transplantation (LT) or death with the latter two adjusted as competing risks.

Results

A total of 269 ALC patients were included: male (72.5%), Caucasian (98.9%), median age 56 years, and median Child-Pugh score 7. The median aMAP score was 60: 12.3% low-risk, 35.3% medium-risk and 52.4% high-risk. After a median follow-up of 41 months, 14 patients developed HCC, 27 received LT and 104 died. The aMAP score predicted HCC development (hazard ratio 1.12 per point increase, P < .001) with good separation of cumulative incidence function between risk groups. The area under the time-dependent receiver operating characteristics curve for predicting HCC development was 0.83 at 1 year and 0.82 at 5 years which was similar to ADRESS-HCC and Veterans Affairs Healthcare System scores respectively.

Conclusions

We validated the excellent performance of the aMAP score in ALC and affirm its applicability across wider aetiologies.

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