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Low-dose aspirin use and survival in breast cancer patients: A nationwide cohort study

TLDR
Little evidence of an association between post-diagnostic low-dose aspirin use and cancer-specific mortality is found in this large nationwide study of breast cancer patients.
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This article is published in Cancer Epidemiology.The article was published on 2017-04-01 and is currently open access. It has received 17 citations till now. The article focuses on the topics: Breast cancer & Cancer registry.

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Complex roles of the old drug aspirin in cancer chemoprevention and therapy.

TL;DR: This review focuses on recent progress in the use of aspirin for cancer chemoprevention and therapy, and integratively analyzes the mechanisms underlying the anticancer effects of aspirin and its metabolites.
Journal ArticleDOI

No association between low-dose aspirin use and breast cancer outcomes overall: a Swedish population-based study

TL;DR: There was no evidence that low-dose aspirin use before or after breast cancer diagnosis is associated with a reduced risk of adverse outcomes overall in breast cancer, and a potential benefit was noted among women with stage I tumors.
Journal ArticleDOI

Aspirin and cancer survival: a systematic review and meta-analyses of 118 observational studies of aspirin and 18 cancers

TL;DR: There is a considerable body of evidence suggestive of about a 20% reduction in mortality in patients with cancer who take aspirin, and the benefit appears not to be restricted to one or a few cancers.
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Concurrent new drug prescriptions and prognosis of early breast cancer: studies using the Danish Breast Cancer Group clinical database.

TL;DR: In this article, the authors suggest that frequently used prescription drugs alter the viability of breast cancer cells in pre-clinical studies and that routine use of these drugs, therefore, may impact brea...
References
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Triple-Negative Breast Cancer: Clinical Features and Patterns of Recurrence

TL;DR: Triple-negative breast cancers have a more aggressive clinical course than other forms of breast cancer, but the adverse effect is transient.
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New ICD-10 version of the Charlson comorbidity index predicted in-hospital mortality

TL;DR: This work represents the first rigorous adaptation of the Charlson comorbidity index for use with ICD-10 data and yields closely similar prevalence and prognosis information by comorbridity category.
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Cyclooxygenase Isozymes: The Biology of Prostaglandin Synthesis and Inhibition

TL;DR: Characterization of the two COX isozymes is allowing the discrimination of the roles each play in physiological processes such as homeostatic maintenance of the gastrointestinal tract, renal function, blood clotting, embryonic implantation, parturition, pain, and fever.
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Overadjustment bias and unnecessary adjustment in epidemiologic studies.

TL;DR: This work uses causal diagrams and an empirical example (the effect of maternal smoking on neonatal mortality) to illustrate and clarify the definition of overadjustment bias, and to distinguish over adjustment bias from unnecessary adjustment.
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Problem of immortal time bias in cohort studies: example using statins for preventing progression of diabetes.

TL;DR: Immortal time in observational studies can bias the results in favour of the treatment group, but it is not difficult to identify and avoid.
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Frequently Asked Questions (8)
Q1. What are the contributions in "Low-dose aspirin use and survival in breast cancer patients: a nationwide cohort study" ?

In this paper, the authors investigated whether post-diagnostic low-dose aspirin use was associated with a decreased risk of death from breast cancer in a large nation-wide cohort of breast cancer patients diagnosed in Scotland. 

It is possible that the extended breast cancer survival observed for aspirin users in these studies may be due to higher PTSG-2 inhibiting doses as opposed to doses which inhibit platelet function. 

In a large breast cancer patient cohort, the authors investigated whether post-diagnostic low-dose aspirin use was associated with a reduction in the risk of breast cancer-specific mortality. 

In a further study of 935 breast cancer patients enrolled in the Carolina Breast Cancer Study, increased duration and regularity of self-reported pre-diagnostic NSAID use (including aspirin) was associated with reduced breast cancer-specific mortality in women with ERpositive tumours while no association was seen for women with ER-negative tumours [34]. 

Deaths were identified from National Records of Scotland with coverage up to 1st January 2015 (or from Scottish Cancer Registry death records) with breast cancer-specific deaths defined as those with breast cancer as the underlying cause of death (ICD code C50). 

Cox regression models were used to calculate hazard ratios (HR) and 95% CIs for breast cancer-specific and all-cause mortality by post-diagnostic low-dose aspirin use. 

post-diagnostic low-dose aspirin use was associated with an increase in all-cause mortality (HR 2.18, 95% CI 1.99, 2.40) which weakened in adjusted analysis but remained statistically significant (adjusted HR 1.21 1.04, 1.40). 

Misclassification of drug use is possible as over-the-counter use of low-dose aspirin was not accounted for, although previous evidence suggests that the majority of chronic aspirin use in administrative prescribing databases is captured [37].