Evidence map›Paper›PMID 39548013›Full record

ArticleBreast cancer research and treatment2025

Trajectories of antidepressant use after tamoxifen initiation among young and middle-aged women with breast cancer.

Oluwadamilola Onasanya, Paula Rosenblatt, Susan dosReis, Eberechukwu Onukwugha, Zafar Zafari, Wendy Camelo Castillo

Abstract read
PubMed Publisher
In one paragraph

Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Oluwadamilola OnasanyaDepartment of Practice, Sciences, and Health Outcomes Research, School of Pharmacy, University of Maryland Baltimore, 220 N Arch Street- 12th Floor, Baltimore, MD, 21201, USA.
Paula RosenblattDivision of Hematology and Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Susan dosReisDepartment of Practice, Sciences, and Health Outcomes Research, School of Pharmacy, University of Maryland Baltimore, 220 N Arch Street- 12th Floor, Baltimore, MD, 21201, USA.
Eberechukwu OnukwughaDepartment of Practice, Sciences, and Health Outcomes Research, School of Pharmacy, University of Maryland Baltimore, 220 N Arch Street- 12th Floor, Baltimore, MD, 21201, USA.
Zafar ZafariDepartment of Practice, Sciences, and Health Outcomes Research, School of Pharmacy, University of Maryland Baltimore, 220 N Arch Street- 12th Floor, Baltimore, MD, 21201, USA.
Wendy Camelo CastilloDepartment of Practice, Sciences, and Health Outcomes Research, School of Pharmacy, University of Maryland Baltimore, 220 N Arch Street- 12th Floor, Baltimore, MD, 21201, USA. wcastillo@rx.umaryland.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAntidepressant treatment patterns may change after women with breast cancer (BC) initiate tamoxifen, potentially impacting health outcomes. We characterized trajectories of antidepressant use after initiating tamoxifen among young and middle-aged women with BC, identifying risk factors for trajectory group membership.

methodsA retrospective cohort included women 18-64 years-old with BC and antidepressant treatment history who received a new tamoxifen dispensing (index date). We measured longitudinal antidepressant use post-index date as 12, monthly, proportion of days covered (PDC) measurements in a 25% random sample of IQVIA PharMetrics® Plus for Academics US claims, 2006-2022. Group-based trajectory models identified latent subgroups of antidepressant use by testing 2-6-group representations; the best model fit determined by the lowest Bayesian Information Criterion, clinical interpretability, and each subgroup comprising ≥ 5% of the cohort. Using multinomial logistic regression, baseline covariates including demographics, depression status and the CYP2D6-inhibitory strength of antidepressants were evaluated as risk factors for the trajectory of antidepressant use after tamoxifen initiation.

resultsOur sample of 851 women followed four distinct antidepressant adherence trajectories after tamoxifen initiation: 12% exhibited immediately decreasing use [mean PDC (sd) 8% (± 7)]; 7% exhibited delayed decreasing use [41% (± 14)]; 20% exhibited dynamic-moderate use [54% (± 15)]; and 60% exhibited consistently high use [91% (+ 7)]. Age, depression, and treatment with non CYP2D6-inhibiting antidepressants were associated with women's trajectory of antidepressant use after initiating tamoxifen.

conclusionNearly 40% of women were nonadherent to antidepressants after tamoxifen initiation. Future research should explore cancer-related and mental health implications of this nonadherence.

Indexed as

Antidepressive AgentsAntineoplastic Agents, HormonalBreast NeoplasmsDepressionTamoxifenAdolescentAdultFemaleHumansMiddle AgedRetrospective StudiesRisk FactorsYoung AdultAntidepressive AgentsAntineoplastic Agents, HormonalTamoxifenAdherenceAntidepressantsBreast cancerCancer survivorshipGroup-based trajectory modelingTamoxifen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.