Evidence map›Paper›PMID 39610376›Full record

ArticleiScience2024

Pembrolizumab followed by irreversible electroporation of a liver metastasis in pancreatic cancer patients.

Rasmus Virenfeldt Flak, Emil Kofod-Olsen, Nikolaj Dich Sølvsten, Gintare Naujokaite, Ralf Agger, Mogens Tornby Stender, Signe Christensen, Susy Shim, Laurids Østergaard Poulsen, Sönke Detlefsen and 2 more

Abstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rasmus Virenfeldt FlakDepartment of Gastrointestinal Surgery and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Emil Kofod-OlsenDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Nikolaj Dich SølvstenDepartment of Gastrointestinal Surgery and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Gintare NaujokaiteDepartment of Radiology, Aalborg University Hospital, Aalborg, Denmark.
Ralf AggerDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Mogens Tornby StenderDepartment of Gastrointestinal Surgery and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Signe ChristensenDepartment of Oncology and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Susy ShimDepartment of Oncology and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Laurids Østergaard PoulsenDepartment of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Sönke DetlefsenDepartment of Pathology, Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.
Ole Thorlasius-UssingDepartment of Gastrointestinal Surgery and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Morten LadekarlDepartment of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preclinical studies suggest that irreversible electroporation (IRE) increases the effect of immune checkpoint inhibition in pancreatic cancer (PC). Patients with PC received PD-1 inhibitor pembrolizumab and, on day 10, percutaneous IRE of a liver metastasis. Blood samples were analyzed for immune cell subsets and inflammation related proteins. mRNA expression profiling was done in sequential biopsies. Treatment was safe, but the trial was terminated early. The response rate in eight patients was 0% and tumor growth was exponential. A drop in circulating plasmacytoid dendritic cells and a rise in several cytokines and proteins, especially PD-1, after immunotherapy was observed. In liver metastases, immune stimulatory genes were upregulated and immune suppressive genes were downregulated after pembrolizumab, while markers of effector T cells were unchanged. Treatment was safe but showed no efficacy in PC. Immunotherapy induced an immune permissive tumor microenvironment but with no increase in effector cells.

Indexed as

clinical findingclinical stageHealth sciencesoncology

Identifiers

PMID39610376
PMCPMC11602522

What Socratic 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 Socratic graph.