Vitamin D Levels in Patients with Colorectal Cancer Before and After Treatment Initiation.


Journal

Journal of gastrointestinal cancer
ISSN: 1941-6636
Titre abrégé: J Gastrointest Cancer
Pays: United States
ID NLM: 101479627

Informations de publication

Date de publication:
Dec 2019
Historique:
pubmed: 31 7 2018
medline: 6 5 2020
entrez: 31 7 2018
Statut: ppublish

Résumé

We aimed to described 25-hydroxyvitamin D [25(OH)D] levels in newly diagnosed colorectal cancer (CRC) patients and to re-evaluate levels after chemotherapy. Permanent residents of the San Francisco Bay Area with a new CRC diagnosis of any stage were recruited prior to any non-surgical therapy. Serum 25(OH)D levels were measured at time of diagnosis and 6-month follow-up. Supplement use was not restricted. The primary endpoint was the frequency of vitamin D deficiency in patients with newly diagnosed CRC of all stages. The Kruskal-Wallis and Spearman correlation tests were used to evaluate associations of patient characteristics with 25(OH)D levels. Median 25(OH)D level at baseline was 27.0 ng/mL (range 7.2, 59.0); 65% of patients had insufficient levels (25(OH)D < 30 ng/mL) (n = 94). Race, disease stage, multivitamin use, vitamin D supplementation, and county of residence were associated with baseline 25(OH)D levels (P < 0.05). The median change in 25(OH)D from baseline to 6 months was - 0.7 ng/mL [- 19.4, 51.7] for patients treated with chemotherapy (n = 58) and 1.6 ng/mL [- 6.4, 33.2] for patients who did not receive chemotherapy (n = 19) (P = 0.26). For patients who received vitamin D supplementation during chemotherapy, the median 25(OH)D change was 8.3 ng/mL [- 7.6, 51.7] versus - 1.6 [- 19.4, 24.3] for chemotherapy patients who did not take vitamin D supplements (P = 0.02). Among patients with a new diagnosis of CRC, most patients were found to have 25(OH)D levels consistent with either deficiency or insufficiency. In the subset of patients who received chemotherapy and took a vitamin D supplement, serum 25(OH)D levels increased, suggesting that vitamin D repletion is a feasible intervention during chemotherapy.

Identifiants

pubmed: 30058032
doi: 10.1007/s12029-018-0147-7
pii: 10.1007/s12029-018-0147-7
pmc: PMC6650370
mid: NIHMS1029046
doi:

Substances chimiques

Vitamins 0
Vitamin D 1406-16-2
25-hydroxyvitamin D A288AR3C9H

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

769-779

Subventions

Organisme : NCI NIH HHS
ID : K07 CA197077
Pays : United States
Organisme : NCI NIH HHS
ID : K08 CA175153
Pays : United States

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Auteurs

Marissa B Savoie (MB)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.

Alan Paciorek (A)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.

Li Zhang (L)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Erin L Van Blarigan (EL)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.

Nilli Sommovilla (N)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.

Donald Abrams (D)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Chloe E Atreya (CE)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Emily K Bergsland (EK)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Hueylan Chern (H)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Colorectal Surgery, University of California, San Francisco, CA, USA.

Robin K Kelley (RK)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Andrew Ko (A)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Angela Laffan (A)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.

Ankit Sarin (A)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Colorectal Surgery, University of California, San Francisco, CA, USA.

Madhulika G Varma (MG)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Colorectal Surgery, University of California, San Francisco, CA, USA.

Alan P Venook (AP)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA.

Katherine Van Loon (K)

UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA. katherine.vanloon@ucsf.edu.
Department of Medicine, Division of Hematology/Oncology, University of California, San Francisco, CA, USA. katherine.vanloon@ucsf.edu.

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Classifications MeSH