Abstract

BackgroundNearly 50% of breast cancer patients suffer from depression or anxiety. Selective serotonin reuptake inhibitors (SSRIs), the first-line pharmacological treatment for depression, have been implicated in breast cancer development through increased prolactin levels and tamoxifen metabolism inhibition. Previous studies of breast cancer progression have focused on tamoxifen users, or have been limited by their small sample size and methodology. Therefore, we used UK population-based data to more robustly investigate the association between SSRI use and cancer-specific mortality.MethodsA cohort of patients with newly-diagnosed breast cancer between 1998 and 2012 was selected from English cancer registries and linked to prescription records from the Clinical Practice Research Datalink, and to death records from the Office for National Statistics. We used Cox regression models to calculate hazard ratios (HRs) comparing mortality between post-diagnostic SSRI users and non-users (using time-dependant covariates), after adjusting for demographics, comorbidities and pre-diagnosis use of hormone replacement therapy or oral contraceptives. We conducted several additional analyses to assess causality.ResultsOur cohort included 23,669 breast cancer patients, of which 2672 used SSRIs and 3053 died due to their breast cancer during follow-up. After adjustment, SSRI users had higher breast cancer-specific mortality than non-users (HR = 1.27; 95% confidence interval (CI) 1.16, 1.40). However, this association was attenuated when restricting to patients with a prior history of depression (HR = 1.14; 95% CI 0.98, 1.33), and when comparing to users of other antidepressant medications (HR = 1.06; 95% CI 0.93, 1.20). There was some evidence of higher mortality among long-term SSRI users, even when restricting to patients with prior depression (HR = 1.54; 95% CI 1.03, 2.29).ConclusionsIn this large breast cancer cohort, SSRI use was associated with a 27% increase in breast cancer mortality. The cause of this is unknown; however, confounding by indication seems likely as it was largely attenuated when restricting to patients with prior depression, or when comparing SSRIs to other antidepressant medications. Clinicians should not be unduly concerned when prescribing SSRIs to breast cancer patients, but the increase in mortality among long-term SSRI users warrants further investigation.

Highlights

  • 50% of breast cancer patients suffer from depression or anxiety

  • Cohort description We identified 27,008 breast cancer cases with no prior cancer diagnosis registered at Clinical Practice Research Datalink (CPRD) practices

  • Association between antidepressant use and survival Selective serotonin reuptake inhibitor (SSRI) users were at a higher risk of breast cancer death than SSRI non-users after adjustment for demographics, comorbidities and pre-diagnosis use of hormone replacement therapy or oral contraceptives

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Summary

Introduction

50% of breast cancer patients suffer from depression or anxiety. Selective serotonin reuptake inhibitors (SSRIs), the first-line pharmacological treatment for depression, have been implicated in breast cancer development through increased prolactin levels and tamoxifen metabolism inhibition. In England, around 15% of patients die due to the disease within 5 years [3]. Breast cancer patients are highly susceptible to mental health problems with nearly 50% suffering depression or anxiety [8], and 10–20% experiencing a major depressive episode after diagnosis [9, 10]. Selective serotonin reuptake inhibitors (SSRIs) are a group of antidepressant medications recommended for moderate/severe depression and treatment-resistant mild depression [11]. In England, 36 million prescriptions were dispensed during 2016, representing a 6% rise on the previous year [12]. SSRIs are widely used among breast cancer patients, mainly to treat depression, and to control hot flushes [15, 16]

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