Evidence map›Paper›PMID 27683115›Full record

ArticleOncotarget2016

CD8+/FOXP3+ ratio and PD-L1 expression associated with survival in pT3N0M0 stage esophageal squamous cell cancer.

Yingming Zhu, Minghuan Li, Dianbin Mu, Li Kong, Jianbo Zhang, Fen Zhao, Zhenxiang Li, Xuemei Liu, Cong Bo, Jinming Yu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 5 pooled it
3.2field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 5 syntheses or guidelines pooled it, 59 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

10 authors at 3 institutions in 1 country.

Yingming ZhuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Minghuan LiDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Dianbin MuDepartment of Pathology, Shandong Cancer Hospital and Institute, Shandong University Jinan, China.
Li KongDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Jianbo ZhangDepartment of Pathology, Shandong Cancer Hospital and Institute, Shandong University Jinan, China.
Fen ZhaoDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Zhenxiang LiDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Xuemei LiuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Cong BoDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Jinming YuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Shandong University · CNShandong First Medical University · CNShandong Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Data describing relationships between the tumor immune microenvironment and patient outcome are limited for esophageal squamous cell cancer (ESCC). The present study investigated the prognostic values of programmed death-ligand 1 (PD-L1) expression and CD8+ or forkhead box protein 3+ (FOXP3+) tumor-infiltrating lymphocytes (TILs) in 133 pathological T3N0M0 stage ESCC patients who underwent radical resection without neoadjuvant or adjuvant therapy. CD8+ and FOXP3+ TIL densities as well as PD-L1 levels in tumor cells and lymphocytes, were assessed through immunohistochemical staining. Patient survival was not associated with CD8+ or FOXP3+ TILs alone, but PD-L1 expression and the CD8+/FOXP3+ ratio were independent predictors of both disease-free and overall survival. PD-L1 expression correlated with age (p = 0.029), tumor length (p < 0.001), tumor differentiation status (p = 0.002) and reduced intratumoral CD8+ TIL density (p < 0.001). Our results suggest pT3N0M0 ESCC clinical outcomes correlate with CD8+ and FOXP3+ TIL densities and PD-L1 levels. Moreover, an intrinsic mechanism for induction of PD-L1 overexpression may be occurring during early tumor oncogenesis. This information may be useful for stratifying patients and guide the application of checkpoint blockade therapy in ESCC.

Indexed as

AdultAgedB7-H1 AntigenCarcinoma, Squamous CellCD8 AntigensEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleForkhead Transcription FactorsHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedNeoplasm StagingPrognosisTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanCD8 AntigensForkhead Transcription FactorsFOXP3 protein, humanCD8esophageal squamous cell cancerforkhead box protein 3programmed death receptor ligand-1pT3N0M0

Identifiers

PMID27683115
PMCPMC5342092
OpenAlexW2521930878

What OpenQuestion holds

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Registered trials

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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.