Evidence map›Paper›PMID 32259711›Full record

ArticleEBioMedicine2020

Evolution of the immune landscape during progression of pancreatic intraductal papillary mucinous neoplasms to invasive cancer.

Susanne Roth, Katharina Zamzow, Matthias M Gaida, Mathias Heikenwälder, Christine Tjaden, Ulf Hinz, Promita Bose, Christoph W Michalski, Thilo Hackert

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.0field-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

41 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Tumor-Derived LAMB3 Drives Immunosuppressive LRRC15Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
  4. Pancreatic cancer.Nature reviews. Disease primers · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Pancreatic cancer is feeling the heat.Journal for immunotherapy of cancer · 2024
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

9 authors at 3 institutions in 1 country.

Susanne RothDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany. Electronic address: susanne.roth@med.uni-heidelberg.de.
Katharina ZamzowDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany.
Matthias M GaidaInstitute of Pathology, Heidelberg University Hospital, Heidelberg, Germany; Institute of Pathology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Mathias HeikenwälderDivision of Chronic Inflammation and Cancer, German Cancer Research Center, Heidelberg, Germany.
Christine TjadenDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany.
Ulf HinzDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany.
Promita BoseDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany.
Christoph W MichalskiDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany; Department of Surgery, Halle University Hospital, Halle (Saale), Germany.
Thilo HackertDepartment of Surgery, Heidelberg University Hospital, Heidelberg, Germany.
Heidelberg University · DEGerman Cancer Research Center · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraductal papillary mucinous neoplasms (IPMNs) are precursor lesions of pancreatic cancer, which is characterized by an immunosuppressive microenvironment. Yet, the spatial distribution of the immune infiltrate and how it changes during IPMN progression is just beginning to be understood.

methodsWe obtained tissue samples from patients who underwent pancreatic surgery for IPMN, and performed comprehensive immunohistochemical analyses to investigate the clinical significance, composition and spatial organization of the immune microenvironment during progression of IPMNs. Survival analysis of pancreatic cancer patients was stratified by tumour infiltrating immune cell subtypes.

findingsThe immune microenvironment evolves from a diverse T cell mixture, comprising CD8

interpretationThe major change with regards to T cell composition during IPMN progression occurs at the step of tissue invasion, indicating that malignant transformation only occurs when tumour immune surveillance is overcome. This suggests that novel immunotherapies that would boost spontaneous antitumor immunity at premalignant states could prevent pancreatic cancer development.

fundingThe present work was supported by German Cancer Aid grants (70,112,720 and 70,113,167) to S. R., and the Olympia Morata Programme of the Medical Faculty of Heidelberg University to S. R.

Indexed as

AgedFemaleHumansMaleMiddle AgedNeoplasm InvasivenessPancreatic Intraductal NeoplasmsT-Lymphocyte SubsetsTumor MicroenvironmentIntraductal papillary mucinous neoplasmPancreatic cancerPremalignant lesionTumour immunologyTumour microenvironment

Identifiers

PMID32259711
PMCPMC7132171
OpenAlexW3015059101

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.