Evidence map›Paper›PMID 27536144›Full record

ArticleOncoTargets and therapy2016

Increased programmed death ligand-1 expression predicts poor prognosis in hepatocellular carcinoma patients.

Xiaobin Gu, Xian-Shu Gao, Wei Xiong, Wei Guo, Linjun Han, Yun Bai, Chuan Peng, Ming Cui, Mu Xie

Abstract read
In one paragraph

Article in OncoTargets and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  3. Establishing peripheral PD-L1 as a prognostic marker in hepatocellular carcinoma patients: how long will it come true?Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

9 authors.

Xiaobin GuDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.
Xian-Shu GaoDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.
Wei XiongDepartment of Oncology, Tangshan People's Hospital, Hebei, People's Republic of China.
Wei GuoGraduate School of Medicine, Hebei North University, Zhangjiakou, Hebei, People's Republic of China.
Linjun HanGraduate School of Medicine, Hebei North University, Zhangjiakou, Hebei, People's Republic of China.
Yun BaiDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.
Chuan PengDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.
Ming CuiDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.
Mu XieDepartment of Radiation Oncology, Peking University First Hospital, Peking University, Beijing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccumulating studies have investigated the prognostic and clinical significance of programmed death ligand-1 (PD-L1) expression in patients with hepatocellular carcinoma (HCC); however, the results were conflicting and inconclusive. We conducted a meta-analysis to combine controversial data to precisely evaluate this issue.

methodsRelevant studies were thoroughly searched on PubMed, Web of Science, and Embase until April 2016. Eligible studies were evaluated by selection criteria. Hazard ratio (HR) with 95% confidence interval (CI) was used to estimate the prognostic role of PD-L1 for overall survival (OS) and disease-free survival (DFS)/recurrence-free survival (RFS). Odds ratio (OR) with 95% CI were selected to assess the relationship between PD-L1 and clinicopathological features of HCC patients. Publication bias was tested using Begg's funnel plot.

resultsA total of seven studies published from 2009 to 2016 were included for meta-analysis. The data showed that high PD-L1 expression was correlated to shorter OS (HR =2.09, 95% CI: 1.66-2.64, P<0.001) as well as poor DFS/RFS (HR =2.3, 95% CI: 1.46-3.62, P<0.001). In addition, increased PD-L1 expression was also associated with tumor differentiation (HR =1.51, 95% CI: 1-2.29, P=0.05), vascular invasion (HR =2.16, 95% CI: 1.43-3.27, P<0.001), and α-fetoprotein (AFP; HR =1.46, 95% CI: 1-2.14, P=0.05), but had no association with tumor stage, tumor size, hepatitis history, sex, age, or tumor multiplicity. No publication bias was found for all analyses.

conclusionThis meta-analysis revealed that overexpression of PD-L1 was predictive for shortened OS and DFS/RFS in HCC. Furthermore, increased PD-L1 expression was associated with less differentiation, vascular invasion, and AFP elevation.

Indexed as

hepatocellular carcinomameta-analysisprognosisprogrammed death ligand-1

Identifiers

PMID27536144
PMCPMC4976917

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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.