Evidence map›Paper›PMID 32309319›Full record

ArticleAnnals of translational medicine2020

Myeloid derived suppressor cells are reduced and T regulatory cells stabilised in patients with advanced pancreatic cancer treated with gemcitabine and intravenous omega 3.

John Isherwood, Ali Arshad, Wen Yuan Chung, Franscois Runau, Jill Cooke, Cristina Pollard, Lynne Howells, Jenny Fishwick, John Thompson, Matthew Metcalfe and 2 more

Open access · diamondAbstract read
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Article in Annals of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 17 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 3 institutions in 1 country.

John IsherwoodDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Ali ArshadDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Wen Yuan ChungDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Franscois RunauDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Jill CookeDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Cristina PollardDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Lynne HowellsLeicester Cancer Research Centre, Leicester Royal Infirmary, Leicester, UK.
Jenny FishwickLeicester Cancer Research Centre, Leicester Royal Infirmary, Leicester, UK.
John ThompsonDepartment of Health Sciences, University of Leicester, Leicester, UK.
Matthew MetcalfeDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
William StewardLeicester Cancer Research Centre, Leicester Royal Infirmary, Leicester, UK.
Ashley DennisonDepartment of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK.
Leicester General Hospital · GBLeicester Royal Infirmary · GBUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic adenocarcinoma (PAC) is a devastating condition, with the majority of patients presenting with metastatic or locally advanced disease. In these patients their disease is classified as advanced pancreatic cancer (APC), which is incurable and associated with survivals generally of a few months. The overall survival (OS) for pancreatic cancer has not changed significantly in the past forty years with multiple trials demonstrating disappointing results. Immune modulatory cells particularly myeloid derived suppressor cells (MDSCs) and T regulatory cells (Tregs) are important mediators in PAC. Omega 3 fatty acids (ω-3FAs) have been shown to have anti-inflammatory properties and there is now evidence demonstrating the benefit of ω-3FAs in PAC.

methodsThis was a single-center cohort study investigating intravenous ω-3FAs and gemcitabine chemotherapy versus gemcitabine therapy only in patients with APC. Here, we investigated levels of MDSCs and Tregs and examined how these changes correlated with survival.

resultsEighteen trial and nine control patients were recruited. There was a significant benefit in progression-free survival (PFS) in trial compared to control patients (P=0.0003). Median survival in trial patients was 5.65 months compared to 1.8 months in control patients. There was no significant benefit in OS in trial compared to control patients (P=0.13). Median survival in trial patients was 7 months compared to 2.9 months in control patients. MDSCs were significantly decreased in trial patients (P=0.0001) but not control patients. Conversely Tregs were significantly increased in control patients (P=0.005) but not in trial patients.

conclusionsAdministration of ω-3FAs with gemcitabine chemotherapy in APC results in a significant decrease of MDSCs and stability of Tregs. This may be secondary to the reduction of pro-inflammatory mediators. A phase three randomized trial is justified to further examine these effects.

Indexed as

myeloid derived suppressor cells (MDSCs)omega 3 fatty acids (ω-3FAs)Pancreatic cancerT regulatory cells (Tregs)

Identifiers

PMID32309319
PMCPMC7154395
OpenAlexW3006803097

What OpenQuestion holds

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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.