Plasma 25-Hydroxyvitamin D Levels and Survival in Stage III Colon Cancer: Findings from CALGB/SWOG 80702 (Alliance).


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
14 Jul 2023
Historique:
received: 13 02 2023
revised: 03 04 2023
accepted: 08 05 2023
pmc-release: 14 01 2024
medline: 17 7 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: ppublish

Résumé

To assess whether higher plasma 25-hydroxyvitamin D [25(OH)D] is associated with improved outcomes in colon cancer and whether circulating inflammatory cytokines mediate such association. Plasma samples were collected from 1,437 patients with stage III colon cancer enrolled in a phase III randomized clinical trial (CALGB/SWOG 80702) from 2010 to 2015, who were followed until 2020. Cox regressions were used to examine associations between plasma 25(OH)D and disease-free survival (DFS), overall survival (OS), and time to recurrence (TTR). Mediation analysis was performed for circulating inflammatory biomarkers of C-reactive protein (CRP), IL6, and soluble TNF receptor 2 (sTNF-R2). Vitamin D deficiency [25(OH)D <12 ng/mL] was present in 13% of total patients at baseline and in 32% of Black patients. Compared with deficiency, nondeficient vitamin D status (≥12 ng/mL) was significantly associated with improved DFS, OS, and TTR (all Plog-rank<0.05), with multivariable-adjusted HRs of 0.68 (95% confidence interval, 0.51-0.92) for DFS, 0.57 (0.40-0.80) for OS, and 0.71 (0.52-0.98) for TTR. A U-shaped dose-response pattern was observed for DFS and OS (both Pnonlinearity<0.05). The proportion of the association with survival that was mediated by sTNF-R2 was 10.6% (Pmediation = 0.04) for DFS and 11.8% (Pmediation = 0.05) for OS, whereas CRP and IL6 were not shown to be mediators. Plasma 25(OH)D was not associated with the occurrence of ≥ grade 2 adverse events. Nondeficient vitamin D is associated with improved outcomes in patients with stage III colon cancer, largely independent of circulation inflammations. A randomized trial is warranted to elucidate whether adjuvant vitamin D supplementation improves patient outcomes.

Identifiants

pubmed: 37289007
pii: 727221
doi: 10.1158/1078-0432.CCR-23-0447
pmc: PMC10524689
mid: NIHMS1901788
doi:

Substances chimiques

25-hydroxyvitamin D A288AR3C9H
Interleukin-6 0
Vitamin D 1406-16-2
Vitamins 0
C-Reactive Protein 9007-41-4

Types de publication

Randomized Controlled Trial Clinical Trial, Phase III Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2621-2630

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233320
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233234
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189858
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA205406
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180860
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233163
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233339
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189960
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233337
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180863
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015083
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA169141
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233180
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA196171
Pays : United States
Organisme : NCI NIH HHS
ID : R33 CA160344
Pays : United States

Informations de copyright

©2023 American Association for Cancer Research.

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Auteurs

Qiao-Li Wang (QL)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Chao Ma (C)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Chen Yuan (C)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Qian Shi (Q)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Brian M Wolpin (BM)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Yin Zhang (Y)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Charles S Fuchs (CS)

Genentech and Roche, South San Francisco, California.
Yale Cancer Center, Yale School of Medicine, Smilow Cancer Hospital, New Haven, Connecticut.

Jeffrey Meyer (J)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Tyler Zemla (T)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

En Cheng (E)

Division of Research, Kaiser Permanente Northern California, Oakland, California.

Priya Kumthekar (P)

Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Lou & Jean Malnati Brain Tumor Institute at the Robert H Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.

Katherine A Guthrie (KA)

SWOG Statistics and Data Management Center, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Felix Couture (F)

Hôtel-Dieu de Québec, Quebec, Canada.

Philip Kuebler (P)

Columbus NCI Community Oncology Research Program, Columbus, Ohio.

Pankaj Kumar (P)

Illinois Cancer Care PC, Peoria, Illinois.

Benjamin Tan (B)

Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri.

Smitha Krishnamurthi (S)

Cleveland Clinic Lerner College of Medicine, Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.

Richard M Goldberg (RM)

West Virginia University Cancer Institute, Morgantown, West Virginia.

Alan Venook (A)

University of California, San Francisco, California.

Charles Blanke (C)

SWOG Cancer Research Network Group Chair's Office, Oregon Health and Science University Knight Cancer Institute, Portland, Oregon.

Anthony F Shields (AF)

Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan.

Eileen M O'Reilly (EM)

Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical Center, New York, New York.

Jeffrey A Meyerhardt (JA)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

Kimmie Ng (K)

Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.

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