Evidence map›Paper›PMID 32852885›Full record

ArticleJournal of viral hepatitis2021

Reappraisal of the diagnostic value of alpha-fetoprotein for surveillance of HBV-related hepatocellular carcinoma in the era of antiviral therapy.

Xiangjun Qian, Shuhong Liu, Huiling Long, Siyu Zhang, Xiaotong Yan, Mingjie Yao, Jiyuan Zhou, Jiao Gong, Jianwen Wang, Xiajie Wen and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of viral hepatitis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 1 country.

Xiangjun QianDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.ORCID 0000-0001-6485-0731
Shuhong LiuDepartment of Pathology and Hepatology, The 5th Medical Centre, Chinese PLA General Hospital, Beijing, China.
Huiling LongDepartment of Infectious Diseases, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Siyu ZhangDepartment of Traditional and Western Medical Hepatology, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
Xiaotong YanDepartment of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou, China.
Mingjie YaoDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Jiyuan ZhouIntervention and Cell Therapy Center, Peking University Shenzhen Hospital, Shenzhen, China.
Jiao GongDepartment of Laboratory Medicine, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jianwen WangDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Xiajie WenDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Tao ZhouIntervention and Cell Therapy Center, Peking University Shenzhen Hospital, Shenzhen, China.
Xiangwei ZhaiDepartment of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou, China.
Qiang XuDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Ting ZhangDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Xiangmei ChenDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.ORCID 0000-0003-0302-6866
Guoxin HuDepartment of Infectious Diseases, Peking University Shenzhen Hospital, Shenzhen, China.
Jie WangDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Zhiliang GaoDepartment of Infectious Diseases, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Yuemin NanDepartment of Traditional and Western Medical Hepatology, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
Junhui ChenIntervention and Cell Therapy Center, Peking University Shenzhen Hospital, Shenzhen, China.
Bo HuDepartment of Laboratory Medicine, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-0133-9837
Jingmin ZhaoDepartment of Pathology and Hepatology, The 5th Medical Centre, Chinese PLA General Hospital, Beijing, China.
Fengmin LuDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.ORCID 0000-0002-1832-3209
Peking University · CNPeking University Shenzhen Hospital · CNSun Yat-sen University · CNChinese PLA General Hospital · CNHebei Medical University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was designed to explore if antiviral treatment influences the performance of serum alpha-fetoprotein (AFP) for hepatocellular carcinoma (HCC) among the high-risk chronic HBV-infected patients. A total of 5936 patients who had evidence of chronic HBV infection were enrolled from four independent centres in this retrospective study, including 1721 chronic hepatitis B (CHB), 2286 liver cirrhosis (LC), 798 HCC within Milan criteria and 1131 HCC beyond Milan criteria patients. Stratified by whether they received treatment or not, the patients were further divided into antiviral and non-antiviral groups. Then, the performance of AFP for discriminating HCC was evaluated. Patients receiving antivirals had significantly lower median levels of AFP compared with the non-antiviral patients (P < .001), and there were significantly less patients with abnormal AFP levels in antiviral groups (P < .001). Antiviral therapy improved the AUROCs of AFP for discriminating HCC within Milan criteria. When setting the cut-off values at 20 ng/mL and 100 ng/mL as surveillance and confirmatory tests respectively for HCC among patients receiving antiviral treatment, AFP exhibited a significantly higher sensitivity than those of 200 ng/mL and 400 ng/mL, which are currently recommended by some guidelines, without compromising specificity. Further analysis in antiviral patients revealed that serum AFP had better performance for discriminating HCC within Milan criteria in ALT ≤ 1ULN patients than that in ALT > 1ULN patients. In conclusion, in the era of antiviral therapy, serum AFP's surveillance performance was substantially improved for HCC within Milan criteria among the high-risk population of CHB and LC patients.

Indexed as

Carcinoma, HepatocellularLiver Neoplasmsalpha-FetoproteinsAntiviral AgentsHepatitis B virusHumansRetrospective Studiesalpha-FetoproteinsAntiviral Agentsalpha-fetoproteinantiviral treatmenthepatitis B virushepatocellular carcinoma

Identifiers

PMID32852885
PMCPMC7756791
OpenAlexW3081205680

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.