Evidence map›Paper›PMID 39306621›Full record

ArticleAnnals of surgical oncology2024

Plasma Ceramide C24:0/C16:0 Ratio is Associated with Improved Survival in Patients with Pancreatic Ductal Adenocarcinoma.

Joshua D Mitchell, Usman Panni, Nicole Fergestrom, Adetunji T Toriola, Timothy M Nywening, S Peter Goedegebuure, Xuntian Jiang, Jacqueline L Mudd, Yin Cao, Joseph Ippolito and 3 more

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

13 authors.

Joshua D MitchellCardiovascular Division, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Usman PanniDepartment of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Nicole FergestromCenter for Advancing Population Science, Medical College of Wisconsin, Milwaukee, WI, USA.
Adetunji T ToriolaAlvin J Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Timothy M NyweningDepartment of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
S Peter GoedegebuureAlvin J Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Xuntian JiangCardiovascular Division, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Jacqueline L MuddDepartment of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Yin CaoAlvin J Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Joseph IppolitoAlvin J Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Ryan C FieldsAlvin J Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
William G Hawkins *Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
Linda R Peterson *Cardiovascular Division, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA. lpeterso@wustl.edu.

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Washington University SPORE in Pancreatic CancerP50CA196510 · NCI · WASHINGTON UNIVERSITY · PI HAWKINS, WILLIAM G · 2016 to 2020
$10.9M
Washington University SPORE in Pancreatic CancerP50CA272213 · NCI · WASHINGTON UNIVERSITY · PI David G DeNardo, WILLIAM G HAWKINS · 2023 to 2026
$10.7M
NCATS NIH HHS UL1 TR002345NCATS NIH HHS UL1TR002345NCI NIH HHS P50 CA196510NCI NIH HHS P50CA196510NCI NIH HHS P50 CA272213NIDDK NIH HHS P30 DK020579
6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) has a high fatality rate, with surgery as the only curative treatment. Identification of new biomarkers related to survival may help guide discovery of new pathophysiologic pathways and potential therapeutic targets. As long-chain ceramides have been linked to tumor proliferation, we sought to determine if ceramide levels were prognostic in PDAC.

methodsPatients from two phase I studies of PDAC were followed for all-cause mortality. Ceramide levels (C24:0, C22:0, and C16:0) were quantified before treatment and at study intervals. Multivariable Cox regression models assessed the association of ceramide levels and mortality after adjusting for other univariable predictors, including time-dependent tumor resection. The ability of repeated ceramide measures to discriminate patients at risk for mortality was also assessed using multivariable modeling and the c-statistic.

resultsHigher plasma C16:0 concentration was associated with higher all-cause mortality in univariable and multivariable analysis (adjusted hazard ratio [aHR] 1.41, 95% confidence interval [CI] 1.09-1.82; p < 0.01). In contrast, a higher plasma C24:0/C16:0 ratio was associated with lower all-cause mortality in multivariable analysis (aHR 0.69, 95% CI 0.49-0.97; p = 0.032). Discrimination of mortality was significantly improved with the addition of either plasma C16:0 or C24:0/C16:0 levels, with optimal discrimination occurring using repeated measures of the C24:0/C16:0 ratio (c-statistic 0.73 vs. c-statistic 0.66; p < 0.001).

conclusionsHigher plasma C16:0 and lower C24:0/C16:0 ratios are independently associated with mortality in PDAC and show an ability to improve discrimination of mortality in this deadly disease. Further studies are needed to confirm this association and evaluate this novel pathway for potential therapeutic targets.

Indexed as

Biomarkers, TumorCarcinoma, Pancreatic DuctalCeramidesPancreatic NeoplasmsAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisSurvival RateBiomarkers, TumorCeramides

Identifiers

PMID39306621
PMCPMC11616724

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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.