Pre-Surgery Inflammatory and Angiogenesis Biomarkers as Predictors of 12-Month Cancer-Related Distress: Results from the ColoCare Study.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
06 03 2023
Historique:
received: 19 08 2022
revised: 18 11 2022
accepted: 27 12 2022
pubmed: 4 1 2023
medline: 8 3 2023
entrez: 3 1 2023
Statut: ppublish

Résumé

Patients with colorectal cancer commonly suffer from complex psychological distress. Elevated distress may be linked to systemic biomarkers. We investigated associations of biomarkers of inflammation and angiogenesis with cancer-related distress (CTXD) score. N = 315 patients (stage I-IV) from 2 centers of the ColoCare Study were included: Huntsman Cancer Institute and University of Heidelberg. Biomarkers (e.g., IL6, VEGF-A, VEGF-D) were measured in serum collected pre-surgery and 12 months thereafter. The CTXD overall score and 4 subscales were collected 12 months after surgery and dichotomized to investigate biomarkers as predictors of distress 12 months after surgery; adjusted for age, sex, body mass index, tumor stage, center, and baseline levels of biomarkers. Doubling of IL6 predicted future increased risk of overall distress [odds ratio (OR), 1.20; 95% confidence interval (CI), 1.02-1.41; P = 0.03]. VEGF-A-predicted future increased risk of high family strain (VEGF-A: OR, 1.21; 95% CI, 1.01-1.44; P = 0.04) and VEGF-D was associated with medical and financial demands (OR, 1.34; 95% CI, 1.01-1.74; P = 0.03). This is the first study to show that systemic biomarkers are significantly associated with future CTXD score. Distress was not measured at baseline; we cannot rule out ongoing associations of inflammation and distress throughout treatment versus a direct effect of inflammation on distress. Nonetheless, these data add to evidence that biobehavioral processes interact and that systemic biomarkers are associated with cancer-related distress one year after surgery. Exercise and diet interventions that lower systemic cytokine levels may impact longer-term CTXD score and improve quality of life of patients with colorectal cancer.

Sections du résumé

BACKGROUND
Patients with colorectal cancer commonly suffer from complex psychological distress. Elevated distress may be linked to systemic biomarkers. We investigated associations of biomarkers of inflammation and angiogenesis with cancer-related distress (CTXD) score.
METHODS
N = 315 patients (stage I-IV) from 2 centers of the ColoCare Study were included: Huntsman Cancer Institute and University of Heidelberg. Biomarkers (e.g., IL6, VEGF-A, VEGF-D) were measured in serum collected pre-surgery and 12 months thereafter. The CTXD overall score and 4 subscales were collected 12 months after surgery and dichotomized to investigate biomarkers as predictors of distress 12 months after surgery; adjusted for age, sex, body mass index, tumor stage, center, and baseline levels of biomarkers.
RESULTS
Doubling of IL6 predicted future increased risk of overall distress [odds ratio (OR), 1.20; 95% confidence interval (CI), 1.02-1.41; P = 0.03]. VEGF-A-predicted future increased risk of high family strain (VEGF-A: OR, 1.21; 95% CI, 1.01-1.44; P = 0.04) and VEGF-D was associated with medical and financial demands (OR, 1.34; 95% CI, 1.01-1.74; P = 0.03).
CONCLUSIONS
This is the first study to show that systemic biomarkers are significantly associated with future CTXD score. Distress was not measured at baseline; we cannot rule out ongoing associations of inflammation and distress throughout treatment versus a direct effect of inflammation on distress. Nonetheless, these data add to evidence that biobehavioral processes interact and that systemic biomarkers are associated with cancer-related distress one year after surgery.
IMPACT
Exercise and diet interventions that lower systemic cytokine levels may impact longer-term CTXD score and improve quality of life of patients with colorectal cancer.

Identifiants

pubmed: 36595657
pii: 712706
doi: 10.1158/1055-9965.EPI-22-0882
pmc: PMC9991988
mid: NIHMS1862903
doi:

Substances chimiques

Vascular Endothelial Growth Factor D 0
Interleukin-6 0
Vascular Endothelial Growth Factor A 0
Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

363-370

Subventions

Organisme : NCI NIH HHS
ID : R03 CA270473
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA189184
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA206110
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA207371
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA246659
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA254108
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA215134
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA160684
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA042014
Pays : United States

Informations de copyright

©2023 American Association for Cancer Research.

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Auteurs

Clara L Lindley (CL)

Huntsman Cancer Institute, Salt Lake City, Utah.

Biljana Gigic (B)

Department of General, Visceral, and Transplantation Surgery, Heidelberg University Hospital, Heidelberg, Germany.

Anita R Peoples (AR)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

Claire J Han (CJ)

University of Washington, School of Nursing, Seattle, Washington.

Tengda Lin (T)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

Caroline Himbert (C)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

Christy A Warby (CA)

Huntsman Cancer Institute, Salt Lake City, Utah.

Juergen Boehm (J)

Huntsman Cancer Institute, Salt Lake City, Utah.

Sheetal Hardikar (S)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

Anjelica Ashworth (A)

Huntsman Cancer Institute, Salt Lake City, Utah.

Martin Schneider (M)

Department of General, Visceral, and Transplantation Surgery, Heidelberg University Hospital, Heidelberg, Germany.

Alexis Ulrich (A)

Klinik für Allgemein-, Viszeral-, Thorax- und Gefäßchirurgie, Städtische Kliniken Neuss, Neuss, Germany.

Petra Schrotz-King (P)

Division of Preventive Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Jane C Figueiredo (JC)

Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Christopher I Li (CI)

Clinical Research and Public Health Sciences Divisions, Fred Hutchinson Cancer Center, Seattle, Washington.

David Shibata (D)

Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.

Erin M Siegel (EM)

Cancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

Adetunji T Toriola (AT)

Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Siteman Cancer Center, St. Louis, Missouri.

Cornelia M Ulrich (CM)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

Karen L Syrjala (KL)

Clinical Research and Public Health Sciences Divisions, Fred Hutchinson Cancer Center, Seattle, Washington.

Jennifer Ose (J)

Huntsman Cancer Institute, Salt Lake City, Utah.
Department of Population Health Sciences, University of Utah, Utah.

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