Evidence map›Paper›PMID 33590387›Full record

ArticleBreast cancer research and treatment2021

Twenty-year risks of breast cancer-specific mortality for stage III breast cancer in the surveillance, epidemiology, and end results registry.

José P Leone, Bernardo A Leone, Nabihah Tayob, Michael J Hassett, Julieta Leone, Rachel A Freedman, Sara M Tolaney, Eric P Winer, Carlos T Vallejo, Nancy U Lin

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Article in Breast cancer research and treatment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  5. Locally advanced breast cancer.Breast (Edinburgh, Scotland) · 2022
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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

10 authors at 1 institution in 1 country.

José P LeoneDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA. JoseP_Leone@dfci.harvard.edu.ORCID http://orcid.org/0000-0002-8537-652X
Bernardo A LeoneGrupo Oncológico Cooperativo del Sur (GOCS), Neuquén, Argentina.
Nabihah TayobDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Michael J HassettDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Julieta LeoneGrupo Oncológico Cooperativo del Sur (GOCS), Neuquén, Argentina.
Rachel A FreedmanDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Sara M TolaneyDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Eric P WinerDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Carlos T VallejoGrupo Oncológico Cooperativo del Sur (GOCS), Neuquén, Argentina.
Nancy U LinDana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, 02215, USA.
Dana-Farber Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe aimed to report the 20-year risk of breast cancer-specific mortality (BCSM), report the risk of BCSM conditional on having survived 5 years, and identify factors associated with late deaths in stage III breast cancer.

methodsUsing Surveillance, Epidemiology, and End Results data, we included women with stage III breast cancer diagnosed from 1990 to 2005. We excluded women with unknown hormone receptor (HR) status, women who did not undergo resection of the primary tumor or axillary nodes, or unknown cause of death. We estimated risks of BCSM using cumulative incidence function and used Fine and Gray regression to identify factors associated with late deaths.

resultsFinal sample was 36,500 patients with 14 years of median follow-up. For each stage subgroup, the risk of BCSM at 20 years was significantly higher for HR-negative vs HR-positive tumors (IIIA: 49.8% vs 43.2%, P < 0.0001; IIIB: 60.9% vs 47.6%, P < 0.0001; IIIC: 68.7% vs 63.1%, P < 0.0001). Compared with the risks of non-BCSM, the risks of BCSM at 20 years were four times higher in stage IIIC HR-positive disease and seven times higher in stage IIIC HR-negative disease. Risks of BCSM conditional on having survived 5 years depended on tumor size, nodal status, race, and tumor grade for HR-positive disease and depended on tumor size, nodal status, and age for HR-negative disease.

conclusionsIn stage III breast cancer, the risk of BCSM at 20 years is very high and remains important even beyond the first 5 years in both HR-positive and HR-negative disease. Late BCSM depends on traditional clinicopathologic factors.

Indexed as

Breast NeoplasmsFemaleHumansNeoplasm StagingRegistriesSEER ProgramEstrogen receptorHormone receptorLatePrognostic factorsRecurrenceRelapse

Identifiers

PMID33590387
OpenAlexW3131289137

What OpenQuestion holds

Textmetadata
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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.