» Articles » PMID: 26364159

Digoxin Use After Diagnosis of Colorectal Cancer and Survival: a Population-based Cohort Study

Overview
Date 2015 Sep 14
PMID 26364159
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Digoxin has been shown to affect a number of pathways that are of relevance to cancer, and its use has been associated with increased risks of breast and uterus cancer and, more recently, a 40% increase in colorectal cancer risk. These findings raise questions about the safety of digoxin use in colorectal cancer patients, and, therefore, we investigated whether digoxin use after colorectal cancer diagnosis increased the risk of colorectal cancer-specific mortality.

Methods: A cohort of 10,357 colorectal cancer patients newly diagnosed from 1998 to 2009 was identified from English cancer registries and linked to the UK Clinical Practice Research Datalink (to provide digoxin and other prescription records) and to the Office of National Statistics mortality data (to identify 2,724 colorectal cancer-specific deaths). Using time-dependent Cox regression models, unadjusted and adjusted HRs and 95% confidence intervals (CI) were calculated for the association between postdiagnostic exposure to digoxin and colorectal cancer-specific mortality.

Results: Overall, 682 (6%) colorectal cancer patients used digoxin after diagnosis. Digoxin use was associated with a small increase in colorectal cancer-specific mortality before adjustment (HR, 1.25; 95% CI, 1.07-1.46), but after adjustment for confounders, the association was attenuated (adjusted HR, 1.10; 95% CI, 0.91-1.34) and there was no evidence of a dose response.

Conclusions: In this large population-based colorectal cancer cohort, there was little evidence of an increase in colorectal cancer-specific mortality with digoxin use after diagnosis.

Impact: These results provide some reassurance that digoxin use is safe in colorectal cancer patients.

Citing Articles

Association Between Digoxin Use and Cancer Incidence: A Propensity Score-Matched Cohort Study With Competing Risk Analysis.

Tai C, Yang Y, Tseng T, Chang F, Wang H Front Pharmacol. 2021; 12:564097.

PMID: 33867973 PMC: 8044813. DOI: 10.3389/fphar.2021.564097.


Digoxin treatment reactivates in vivo radioactive iodide uptake and correlates with favorable clinical outcome in non-medullary thyroid cancer.

Crezee T, Tesselaar M, Nagarajah J, Corver W, Morreau J, Pritchard C Cell Oncol (Dordr). 2021; 44(3):611-625.

PMID: 33534128 PMC: 8213564. DOI: 10.1007/s13402-021-00588-y.


Multifaceted anti-colorectal tumor effect of digoxin on HCT8 and SW620 cells .

Hou Y, Wang Y, Wang X, Liu Y, Zhang C, Chen Z Gastroenterol Rep (Oxf). 2021; 8(6):465-475.

PMID: 33442480 PMC: 7793120. DOI: 10.1093/gastro/goaa076.


Cancer mortality does not differ by antiarrhythmic drug use: A population-based cohort of Finnish men.

Kaapu K, Rantaniemi L, Talala K, Taari K, Tammela T, Auvinen A Sci Rep. 2018; 8(1):10308.

PMID: 29985440 PMC: 6037774. DOI: 10.1038/s41598-018-28541-4.


Cardiac glycosides use and the risk and mortality of cancer; systematic review and meta-analysis of observational studies.

Osman M, Farrag E, Selim M, Osman M, Hasanine A, Selim A PLoS One. 2017; 12(6):e0178611.

PMID: 28591151 PMC: 5462396. DOI: 10.1371/journal.pone.0178611.