Evidence map›Paper›PMID 28039448›Full record

ArticleOncotarget2017

Independent prognostic role of PD-L1expression in patients with esophageal squamous cell carcinoma.

Dongxian Jiang, Qi Song, Haixing Wang, Jie Huang, Hao Wang, Jun Hou, Xiaojing Li, Yifan Xu, Akesu Sujie, Haiying Zeng and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 pooled it
1.7field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 3 syntheses or guidelines pooled it, 29 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

12 authors at 4 institutions in 1 country.

Dongxian JiangDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Qi SongDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Haixing WangDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Jie HuangDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Hao WangDepartment of thoracic surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Jun HouDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Xiaojing LiDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Yifan XuDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Akesu SujieDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Haiying ZengDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Lijie TanDepartment of thoracic surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Yingyong HouDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, P. R. China.
Sun Yat-sen University · CNFudan University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence has shown that PD-L1 expression is associated with clinicopathological features in various human malignancies. We searched for correlations between PD-L1 expression and clinicopathological data in esophageal squamous cell carcinoma (ESCC) patients. PD-L1 expression in primary tumors from 278 patients was evaluated using immunohistochemistry (IHC) in ESCC tissue microarray. Survival curves were constructed by using the Kaplan-Meier method. Univariate and multivariate Cox proportional hazard regression models were performed to identify associations with outcome variables. Overall, tumoral PD-L1 expression (≥10%, 20% or 30% as cut-off value) was associated with favorable DFS and OS upon multivariate analysis. When the patients stratified into stage I-II (168, 60.4%) and stage III-IV (110, 39.6%), or with lymph node metastasis (133, 47.8%), the prognostic role was not consistent. In patients with stage I-II disease, tumoral PD-L1 expression (≥5%, 10%, 20% or 30%) was associated with better DFS and OS upon multivariate analysis. In patients without lymph node metastasis, tumoral PD-L1 expression (≥1%, 5%, 10%, 20%, or 30%) was associated with improved DFS and OS in univariate or multivariate analysis. However, PD-L1 expression was not correlated with prognosis in patients with stage III-IV disease or with lymph node metastasis. Our results for the first time showed the prognostic role of tumoral PD-L1 expression was variable in different stages and lymph node status of ESCC. Tumoral PD-L1 expression was independent favorable predictor in ESCC patients with Stage I-II disease or without lymph node metastasis, not in stage III-IV or lymph node metastasis.

Indexed as

AdultAgedAged, 80 and overB7-H1 AntigenBiomarkers, TumorCarcinoma, Squamous CellChi-Square DistributionDisease-Free SurvivalDisease ProgressionEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleHumansImmunohistochemistryKaplan-Meier EstimateLymphatic MetastasisB7-H1 AntigenBiomarkers, TumorCD274 protein, humanclinical stageESCClymph node metastasisPD-L1 expressionprognostic marker

Identifiers

PMID28039448
PMCPMC5352403
OpenAlexW2565944822

What OpenQuestion holds

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LicenceCC BY
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.