Evidence map›Paper›PMID 30497874›Full record

ArticlePancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]2019

Circulating interleukin-6 is associated with disease progression, but not cachexia in pancreatic cancer.

Mitchell L Ramsey, Erin Talbert, Daniel Ahn, Tanios Bekaii-Saab, Niharika Badi, P Mark Bloomston, Darwin L Conwell, Zobeida Cruz-Monserrate, Mary Dillhoff, Matthew R Farren and 11 more

Open access · greenAbstract read
In one paragraph

Article in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Prognostic significance of pre-intervention circulating cytokines in digestive system cancers: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  3. The effects of tissue inflammation on cancer cachexia.Biochimica et biophysica acta. Molecular basis of disease · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. The metabolic basis of cancer-related fatigue.Neuroscience and biobehavioral reviews · 2025
    Review
  9. Review
  10. 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

21 authors at 5 institutions in 1 country.

Mitchell L RamseyDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Erin TalbertDepartment of Cancer Biology and Genetics and The Ohio State University Comprehensive Cancer Center Cachexia Program, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Daniel AhnDivision of Hematology/Medical Oncology, Mayo Clinic, Phoenix, AZ, USA.
Tanios Bekaii-SaabDivision of Hematology/Medical Oncology, Mayo Clinic, Phoenix, AZ, USA.
Niharika BadiDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
P Mark Bloomston21st Century Oncology, Inc., Fort Meyers, FL, USA.
Darwin L ConwellDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Zobeida Cruz-MonserrateDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Mary DillhoffDepartment of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Matthew R FarrenDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, USA.
Alice HintonDivision of Biostatistics, The Ohio State University, Columbus, OH, USA.
Somashekar G KrishnaDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Gregory B LesinskiDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA, USA.
Thomas MaceDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Andrei ManilchukDepartment of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Anne NoonanDivision of Medical Oncology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Timothy M PawlikDepartment of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Priyani V RajasekeraDepartment of Cancer Biology and Genetics and The Ohio State University Comprehensive Cancer Center Cachexia Program, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Carl SchmidtDepartment of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Denis GuttridgeDepartment of Cancer Biology and Genetics and The Ohio State University Comprehensive Cancer Center Cachexia Program, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Phil A HartDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA. Electronic address: philip.hart@osumc.edu.
The Ohio State University Wexner Medical Center · USEmory University · USMayo Clinic Hospital · US21st Century Oncology (United States) · USThe Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI WANCAI YANG · 1985 to 2026
$132.3M
The Ohio State University Pancreatic Disorders Network (OSU-PDN)U01DK108327 · NIDDK · OHIO STATE UNIVERSITY · PI CONWELL, DARWIN LEWIS, HART, PHILIP A. · 2015 to 2024
$5.5M
Tumor ImmunologyT32CA090223 · NCI · OHIO STATE UNIVERSITY · PI CARSON, WILLIAM E. · 2002 to 2023
$4.1M
(PQD6) Muscle stem cells and cancer cachexiaR01CA180057 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2013 to 2016
$1.5M
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA180057NCI NIH HHS T32 CA090223NIDDK NIH HHS U01 DK108327
6 · The paper itself

Abstract

backgroundCachexia is a wasting syndrome characterized by involuntary loss of >5% body weight due to depletion of adipose and skeletal muscle mass. In cancer, the pro-inflammatory cytokine interleukin-6 (IL-6) is considered a mediator of cachexia and a potential biomarker, but the relationship between IL-6, weight loss, and cancer stage is unknown. In this study we sought to evaluate IL-6 as a biomarker of cancer cachexia while accounting for disease progression.

methodsWe retrospectively studied 136 subjects with biopsy-proven pancreatic ductal adenocarcinoma (PDAC), considering the high prevalence of cachexia is this population. Clinical data were abstracted from subjects in all cancer stages, and plasma IL-6 levels were measured using a multiplex array and a more sensitive ELISA. Data were evaluated with univariate comparisons, including Kaplan-Meier survival curves, and multivariate Cox survival models.

resultsOn multiplex, a total of 43 (31.4%) subjects had detectable levels of plasma IL-6, while by ELISA all subjects had detectable IL-6 levels. We found that increased plasma IL-6 levels, defined as detectable for multiplex and greater than median for ELISA, were not associated with weight loss at diagnosis, but rather with the presence of metastasis (p < 0.001 for multiplex and p = 0.007 for ELISA). Further, while >5% weight loss was not associated with worse survival, increased plasma IL-6 by either methodology was.

conclusionCirculating IL-6 levels do not correlate with cachexia (when defined by weight loss), but rather with advanced cancer stage. This suggests that IL-6 may mediate wasting, but should not be considered a diagnostic biomarker for PDAC-induced cachexia.

Indexed as

AgedBiomarkers, TumorCachexiaCarcinoma, Pancreatic DuctalDisease ProgressionFemaleHumansInterleukin-6MaleMiddle AgedPancreatic NeoplasmsRetrospective StudiesBiomarkers, TumorIL6 protein, humanInterleukin-6BiomarkerInflammationPancreatic ductal adenocarcinomaWeight loss

Identifiers

PMID30497874
PMCPMC6613190
OpenAlexW2900094529

What OpenQuestion holds

Textmetadata
LicenceTDM
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.