Evidence map›Paper›PMID 39989973›Full record

ArticleResearch square2025

Race-based differences in serum biomarkers for cancer-associated cachexia in a diverse cohort of patients with pancreatic ductal adenocarcinoma.

Jennifer Permuth, Margaret Park, Evan Davis, Solomon Alhassan, J Arnoletti, Toni Basinski, Ashley McKee, Mark Bloomston, Tiffany Carson, Tiago Biachi de Castria and 37 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. 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

5 · Who and what money

Authors and funding

47 authors.

Jennifer PermuthH. Lee Moffitt Cancer Center and Research Institute.ORCID 0000-0002-4726-9264
Margaret ParkH. Lee Moffitt Cancer Center and Research Institute.
Evan DavisH. Lee Moffitt Cancer Center and Research Institute.
Solomon AlhassanH. Lee Moffitt Cancer Center and Research Institute.
J ArnolettiOrlando Health Cancer Institute.
Toni BasinskiH. Lee Moffitt Cancer Center and Research Institute.
Ashley McKeeH. Lee Moffitt Cancer Center and Research Institute.
Mark BloomstonOhio State University.
Tiffany CarsonH. Lee Moffitt Cancer Center and Research Institute.
Tiago Biachi de CastriaH. Lee Moffitt Cancer Center and Research Institute.
Dung-Tsa ChenMoffitt Cancer Center.ORCID 0000-0001-5026-415X
Elena CortizasUniversity of Miami.
Sylvia CrowderH. Lee Moffitt Cancer Center and Research Institute.
Maria Genilo DelgadoH. Lee Moffitt Cancer Center and Research Institute.
Wade DouglasFlorida State University College of Medicine.
Jason FlemingUniversity of Texas Southwestern Medical Center.
Pamela HodulH. Lee Moffitt Cancer Center and Research Institute.
Kevin HuguetSt. Anthony's Hospital.
Kun JiangMoffitt Cancer Center.
Dae Won KimH. Lee Moffitt Cancer Center and Research Institute.
John KoomenMoffitt Cancer Center.ORCID 0000-0002-3818-1762
Anjuli LuthraH. Lee Moffitt Cancer Center and Research Institute.
Mokenge MalafaH. Lee Moffitt Cancer Center and Research Institute.
Anjana MenonH. Lee Moffitt Cancer Center and Research Institute.
Raiza MoralesH. Lee Moffitt Cancer Center and Research Institute.
Nipun MerchantUniversity of Miami.
Kenneth MeredithSarasota Memorial Hospital.
Qianxing MoH. Lee Moffitt Cancer Center and Research Institute.ORCID 0000-0002-0021-7694
Manual Molina-VegaLakeland Heath Regional Hospital.
Lina Moreno-UrazanH. Lee Moffitt Cancer Center and Research Institute.
Kayode OlumoyinH. Lee Moffitt Cancer Center and Research Institute.
Nathan ParkerMoffitt Cancer Center.
Jose PimientoH. Lee Moffitt Cancer Center and Research Institute.
Ghulam RasoolH. Lee Moffitt Cancer Center and Research Institute.
Katarzyna RejniakH. Lee Moffitt Cancer Center and Research Institute.
Samer SansilH. Lee Moffitt Cancer Center and Research Institute.
Lauren SparksTranslational Research Institute, AdventHealth.ORCID 0000-0002-8724-6016
Paul StewartMoffitt Cancer Center.ORCID 0000-0003-0882-308X
Alexandra TassielliH. Lee Moffitt Cancer Center & Research Institute.
Jamie TeerDepartment of Biostatistics and Bioinformatics, Moffitt Cancer Center.ORCID 0000-0003-4513-0282
Dan Viet TranUniversity of Miami Miller School of Medicine.
Jose TrevinoVirginia Commonwealth University.
Vic VelanovichUniversity of South Florida.
Christopher WhelanMoffitt Cancer Center.ORCID 0000-0001-7511-2603
Daniel JeongDepartment of Radiology, Moffitt Cancer Center.
Sarah JudgeDepartment of Physical Therapy, College of Public Health and Health Professions, University of Florida.
Andrew JudgeDepartment of Physical Therapy, College of Public Health and Health Professions, University of Florida.ORCID 0000-0002-4488-291X

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
United for Health Excellence - Living PDX Program (U4HELPP)U54CA283762 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Jose G. Trevino · 2023 to 2026
$5.0M
NCI NIH HHS P30 CA076292NCI NIH HHS P30 CA240139NCI NIH HHS U54 CA283762
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma is projected to become the second leading cause of cancer-related deaths by 2040, with the highest disease burden expected amongst Non-Hispanic Blacks. One of the most significant predictors of poor outcomes is the presence of cancer-associated cachexia (CCa). Yet, race- and ethnicity-specific biomarkers for early CCa diagnosis are lacking. Thus, evaluated a panel of candidate biomarkers of CCa in a diverse cohort of pre-treatment serum. Our study shows that GDF-15 was associated with cachexia severity, was superior to standard CCa-associated biomarkers at classifying cachexia, and differentiated between non-cachexia and pre-cachexia status, but only among Hispanic/Latinx and non-Hispanic Whites. Furthermore, high GDF-15 levels at diagnosis were associated with a ~ 2-fold increase in weight loss over the 6 months post-diagnosis. Thus, GDF-15 may be a potential biomarker for pre-cachexia (prior to weight loss) in the White and the Hispanic population, but not Black individuals. These findings underscore the fact that enrollment of minority individuals in clinical trials to evaluate treatments for CCa is of utmost importance.

Identifiers

PMID39989973
PMCPMC11844656

What OpenQuestion holds

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Registered trials

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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.