Evidence map›Paper›PMID 32196839›Full record

ArticlePharmacoepidemiology and drug safety2020

The impact of generic aromatase inhibitors on initiation, adherence, and persistence among women with breast cancer: Applying multi-state models to understand the dynamics of adherence.

Aaron N Winn, Nicole M Fergestrom, Liliana E Pezzin, Purushottam W Laud, Joan M Neuner

Abstract read
In one paragraph

Article in Pharmacoepidemiology and drug safety, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

5 authors.

Aaron N WinnDepartment of Clinical Sciences, School of Pharmacy, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0000-0003-2906-3913
Nicole M FergestromCenter for the Advancing Population Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Liliana E PezzinCancer Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Purushottam W LaudCancer Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Joan M NeunerCancer Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0000-0003-0031-5988

Funding

Institutional Career Development CoreKL2TR001438 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI WIDLANSKY, MICHAEL E · 2015 to 2024
$2.9M
Policy-relevant mechanisms of socioeconomic disparities in adherence to oral hormonal therapy for breast cancerR01MD010728 · NIMHD · MEDICAL COLLEGE OF WISCONSIN · PI NEUNER, JOAN MARIE · 2016 to 2019
$2.2M
Mechanisms Underlying SES Disparities in Breast Cancer MortalityR01CA170945 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI NATTINGER, ANN B, PEZZIN, LILIANA E. · 2013 to 2015
$1.2M
NCATS NIH HHS KL2 TR001438NCATS NIH HHS KL2TR001438NCI NIH HHS R01 CA170945NIMHD NIH HHS 1R01MD010728-01NIMHD NIH HHS R01 MD010728
6 · The paper itself

Abstract

purposeClinical trials have clearly documented the survival benefit of aromatase inhibitors (AIs); however, many women fail to initiate (primary nonadherence) or remain adherent to AIs (secondary nonadherence). Prior studies have found that costs impact secondary nonadherence to medications but have failed to examine primary nonadherence. The purpose of this study is to examine primary and secondary adherence following the reduction in copays due to the introduction of generic AIs.

methodsUsing Surveillance, Epidemiology, and End Results-Medicare data, we identified 50 054 women diagnosed with incident breast cancer between 2008 and 2013. We compare women whose copays would change and those whose would not, due to the receipt of cost-sharing subsidies before and after generics were introduced using a difference-in-difference (DinD) analysis. To examine primary and secondary nonadherence, we rely on a multistate model with four states (Not yet initiated, User, Not Using, and Death). We adjusted for baseline factors using inverse probability treatment weights and then simulated adherence for 36 months following diagnosis.

resultsThe generic introduction of AIs resulted in patients initiating AIs faster (DinD = -4.7%, 95%CI = -7.0, -2.3; patients not yet initiating treatment at 6-months), being more adherent (DinD ranging in absolute increase of 8.1%-10.4%) and being less likely to not be using the therapy (DinD range in absolute decrease of 1.2% at 6 months to 8.8% at 24 months) for women that do not receive a subsidy after generics were available.

conclusionsIntroduction of generic alternatives to AIs significantly reduced primary and secondary nonadherence.

Indexed as

Medication AdherenceAgedAged, 80 and overAromatase InhibitorsBreast NeoplasmsCohort StudiesDrugs, GenericFemaleHumansMedicareModels, TheoreticalSEER ProgramSurvival AnalysisUnited StatesAromatase InhibitorsDrugs, Genericadherencebreast cancercopaymentendocrine therapygenericmulti-state modelpharmacoepidemiologysurvival analysis

Identifiers

PMID32196839
PMCPMC11363905

What OpenQuestion holds

Textmetadata
LicenceTDM
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.