Evidence map›Paper›PMID 28429196›Full record

ArticleAnnals of surgical oncology2017

Expression of Programmed Cell Death Protein 1 by Tumor-Infiltrating Lymphocytes and Tumor Cells is Associated with Advanced Tumor Stage in Patients with Esophageal Adenocarcinoma.

Dagmar Kollmann, Desislava Ignatova, Julia Jedamzik, Yun-Tsan Chang, Gerd Jomrich, Matthias Paireder, Ivan Kristo, Dmitry Kazakov, Michal Michal, Antonio Cozzio and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of surgical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Paradoxical effects of adiposity and inflammation on immunotherapy efficacy in gastric cancer: novel insights from real-world data.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The immune landscape of esophageal cancer.Cancer communications (London, England) · 2019
    Review
  13. Clinicopathologic implications of CD8Cancer immunology, immunotherapy : CII · 2018
    Article
  14. Article
  15. Article
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

16 authors at 8 institutions in 4 countries.

Dagmar KollmannDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Desislava IgnatovaDepartment of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
Julia JedamzikDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Yun-Tsan ChangDepartment of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
Gerd JomrichDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Matthias PairederDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Ivan KristoDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Dmitry KazakovDepartment of Pathology, Faculty of Medicine in Plzen and Charles University Hospital Plzen, Biomedical Center, Charles University, Pilsen, Czech Republic.
Michal MichalDepartment of Pathology, Faculty of Medicine in Plzen and Charles University Hospital Plzen, Biomedical Center, Charles University, Pilsen, Czech Republic.
Antonio CozzioDepartment of Dermatology, Kantonspital St. Gallen, University of Zurich, Zurich, Switzerland.
Wolfram HoetzeneckerDepartment of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
Tobias SchattonDepartment of Dermatology, Harvard Skin Disease Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Reza AsariDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Matthias PreusserClinical Division of Oncology, Department of Medicine I and Comprehensive Cancer Center, GET-Unit, Medical University of Vienna, Vienna, Austria.
Emmanuella GuenovaDepartment of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland. emmanuella.guenova@usz.ch.
Sebastian F SchoppmannDepartment of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria. sebastian.schoppmann@meduniwien.ac.at.
Medical University of Vienna · ATComprehensive Cancer Center Vienna · ATCharles University · CZUniversity of Zurich · CHHarvard University · USKantonsspital St. Gallen · CHKepler Universitätsklinikum · ATUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite recent advances in the therapy for adenocarcinoma of the esophagogastric junction (AEG), overall prognosis remains poor. Programmed cell death protein 1 (PD1) is a co-inhibitory receptor primarily expressed by T-cells. Tumor cells can escape anticancer immune responses by triggering the PD1 pathway. Moreover, PD1 receptor engagement on cancer cells may trigger tumor-intrinsic growth signals. This study aimed to evaluate the potential clinical relevance of PD1 expression by tumor-infiltrating lymphocytes (TILs) and cancer cells in the AEG.

methodsPatients with AEG who underwent esophagectomy from 1992 to 2011 were included in the study. Expression of PD1was evaluated by immunohistochemistry and correlated with long-term overall survival (OS), disease-free survival (DFS), and various clinicopathologic parameters.

resultsTumor biospecimens from 168 patients were analyzed. In the analysis, 81% of the patients showed high tumoral frequencies (>5%) of PD1-expressing TILs (TIL-PD1

conclusionsThe PD1 receptor is expressed by both TILs and cancer cells in AEG. High expression of PD1 is associated with advanced tumor stage and lymph node involvement, but not with survival.

Indexed as

Esophagogastric JunctionAdenocarcinomaAdultAgedAged, 80 and overDisease-Free SurvivalEsophageal NeoplasmsFemaleHumansImmunohistochemistryLymphatic MetastasisLymphocytes, Tumor-InfiltratingMaleMiddle AgedNeoplasm StagingProgrammed Cell Death 1 ReceptorPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID28429196
PMCPMC5539275
OpenAlexW2606227520

What OpenQuestion holds

Textmetadata
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.