Evidence map›Paper›PMID 27889052›Full record

ArticleMaturitas2017

Types of oral contraceptives and breast cancer survival among women enrolled in Medicaid: A competing-risk model.

Marsha E Samson, Swann Arp Adams, Caroline M Mulatya, Jiajia Zhang, Charles L Bennett, James Hebert, Susan E Steck

Open access · greenAbstract read
In one paragraph

Article in Maturitas, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 18% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
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

7 authors at 1 institution in 1 country.

Marsha E SamsonCancer Prevention and Control Program, University of South Carolina, United States; Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States. Electronic address: msamson@email.sc.edu.
Swann Arp AdamsCancer Prevention and Control Program, University of South Carolina, United States; Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States; College of Nursing, University of South Carolina, United States.
Caroline M MulatyaEpidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States.
Jiajia ZhangEpidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States.
Charles L BennettCollege of Pharmacy, University of South Carolina, United States.
James HebertCancer Prevention and Control Program, University of South Carolina, United States; Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States.
Susan E SteckCancer Prevention and Control Program, University of South Carolina, United States; Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, United States.
University of South Carolina · US

Funding

Biomedical-Behavioral Interface: Prevention and Developmental Sciences TrainingT32GM081740 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PRINZ, RONALD J · 2008 to 2022
$4.5M
NIGMS NIH HHS T32 GM081740
6 · The paper itself

Abstract

introductionOral contraceptive pills have been implicated in the pathophysiology of breast cancer. Although many studies have examined the relationship between combined oral contraceptives (COCs) and breast cancer, there is a paucity of literature that discusses progestin-only oral contraceptives (POCs) and breast cancer. The purpose of this investigation is to examine potential associations between different types of oral contraceptives and breast cancer mortality in the South Carolina Medicaid population among different racial/ethnic groups.

methodsSubjects included 4816 women diagnosed with breast cancer between 2000 and 2013. Kaplan-Meier curves were calculated to determine time-to-mortality rates among users of oral contraceptives. Competing-risks models and Cox multivariate survival models were used to estimate the hazard ratios (HRs) and 95% confidence intervals (CIs) of breast cancer and other-cause mortality, as well as all-cause mortality.

resultsPOCs were associated with a significantly decreased risk of breast cancer mortality (HR: 0.07; 95% CI: 0.01, 0.52) and a non-significant increased risk of all-cause mortality (HR: 1.04; 95% CI: 0.52, 2.07). COCs increased the risk of breast cancer mortality (HR: 1.61; 95% CI: 1.14, 2.28) and all-cause mortality (HR: 1.83; 95% CI: 1.30, 2.57).

conclusionUse of POCs may be associated with a decreased risk of breast cancer mortality. Due to the small sample size of POC users in the current study, additional research is needed to confirm these findings.

Indexed as

MedicaidAdultBreast NeoplasmsContraceptives, OralFemaleHumansMiddle AgedRiskSurvival RateUnited StatesContraceptives, OralBreast cancerCompeting riskHealth disparitiesOral contraceptivesProgestinSurvival analysis

Identifiers

PMID27889052
PMCPMC5367152
OpenAlexW2551760885

What OpenQuestion holds

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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.