Evidence map›Paper›PMID 34579765›Full record

ArticleBreast cancer research : BCR2021

Modeling risks of cardiovascular and cancer mortality following a diagnosis of loco-regional breast cancer.

Nicole M Leoce, Zhezhen Jin, Rebecca D Kehm, Janise M Roh, Cecile A Laurent, Lawrence H Kushi, Mary Beth Terry

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Nicole M LeoceDepartment of Epidemiology, Joseph L. Mailman School of Public Health, Columbia University, 722 West 168th Street, New York, NY, 161110032, USA.
Zhezhen JinDepartment of Epidemiology, Joseph L. Mailman School of Public Health, Columbia University, 722 West 168th Street, New York, NY, 161110032, USA.
Rebecca D KehmDepartment of Epidemiology, Joseph L. Mailman School of Public Health, Columbia University, 722 West 168th Street, New York, NY, 161110032, USA.
Janise M RohDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Cecile A LaurentDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Lawrence H KushiDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Mary Beth TerryDepartment of Epidemiology, Joseph L. Mailman School of Public Health, Columbia University, 722 West 168th Street, New York, NY, 161110032, USA. mt146@columbia.edu.ORCID 0000-0002-4106-5033

Funding

Prospective Study of Breast Cancer SurvivorshipR01CA105274 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI KUSHI, LAWRENCE H · 2004 to 2014
$19.9M
Infrastructure for Pathways, a Prospective Study of Breast Cancer SurvivorshipU01CA195565 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI AMBROSONE, CHRISTINE B., KUSHI, LAWRENCE H · 2016 to 2025
$18.8M
Training Program in Cancer-Related Population SciencesR25CA094061 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI NEUGUT, ALFRED I. · 2002 to 2016
$5.9M
NCI NIH HHS 5-R25-CA-094061NCI NIH HHS R01 CA105274NCI NIH HHS R01CA105274NCI NIH HHS R25 CA094061NCI NIH HHS U01 CA195565NCI NIH HHS U01CA195565
6 · The paper itself

Abstract

backgroundMany women with breast cancer also have a high likelihood of cardiovascular mortality, and while there are several cardiovascular risk prediction models, none have been validated in a cohort of breast cancer patients. We first compared the performance of commonly-used cardiovascular models, and then derived a new model where breast cancer and cardiovascular mortality were modeled simultaneously, to account for the competing risk endpoints and commonality of risk factors between the two events.

methodsWe included 20,462 women diagnosed with stage I-III breast cancer between 2000 and 2010 in Kaiser Permanente Northern California (KPNC) with follow-up through April 30, 2015, and examined the performance of the Framingham, CORE and SCOREOP cardiovascular risk models by area under the receiver operating characteristic curve (AUC), and observed-to -expected (O/E) ratio. We developed a multi-state model based on cause-specific hazards (CSH) to jointly model the causes of mortality.

resultsThe extended models including breast cancer characteristics (grade, tumor size, nodal involvement) with CVD risk factors had better discrimination at 5-years with AUCs of 0.85 (95% CI 0.83, 0.86) for cardiovascular death and 0.80 (95% CI 0.78, 0.87) for breast cancer death compared with the existing cardiovascular models evaluated at 5 years AUCs ranging 0.71-0.78. Five-year calibration for breast and cardiovascular mortality from our multi-state model was also excellent (O/E = 1.01, 95% CI 0.91-1.11).

conclusionA model incorporating cardiovascular risk factors, breast cancer characteristics, and competing events, outperformed traditional models of cardiovascular disease by simultaneously estimating cancer and cardiovascular mortality risks.

Indexed as

Models, StatisticalAdultAgedAged, 80 and overArea Under CurveBreast NeoplasmsCardiovascular DiseasesCause of DeathCohort StudiesFemaleHumansMiddle AgedRisk FactorsYoung AdultBreast cancerCardiovascular diseaseCardiovascular mortalityRisk prediction models

Identifiers

PMID34579765
PMCPMC8474887

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Registered trials

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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.