Evidence map›Paper›PMID 35752724›Full record

ArticleAnnals of surgical oncology2022

Prevalence of Pathologic N2/N3 Disease in Postmenopausal Women with Clinical N0 ER+/HER2- Breast Cancer.

Maire J Amlicke, Jihye Park, Chris B Agala, Dana L Casey, Emily M Ray, Stephanie M Downs-Canner, Philip M Spanheimer

Open access · greenAbstract read
In one paragraph

Article in Annals of surgical oncology, 2022. 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
1.1field-weighted citation impact, top 23% 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, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Maire J AmlickeDepartment of Surgery, University of North Carolina, Chapel Hill, NC, USA.
Jihye ParkDepartment of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
Chris B AgalaDepartment of Surgery, University of North Carolina, Chapel Hill, NC, USA.
Dana L CaseyDepartment of Radiation Oncology, University of North Carolina, Chapel Hill, NC, USA.
Emily M RayLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Stephanie M Downs-CannerBreast Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Philip M SpanheimerDepartment of Surgery, University of North Carolina, Chapel Hill, NC, USA. Philip_Spanheimer@med.unc.edu.ORCID http://orcid.org/0000-0001-8644-0178
University of North Carolina at Chapel Hill · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHARLES M PEROU · 1992 to 2026
$59.3M
SHORT-TERM RESEARCH TRAININGT35DK007386 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Evan Samuel Dellon · 1986 to 2026
$4.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016086NCI NIH HHS P30CA016086NCI NIH HHS P50 CA058223NCI NIH HHS P50CA058223NIDDK NIH HHS T35 DK007386NIH HHS T35-DK007386
6 · The paper itself

Abstract

backgroundThe RxPONDER trial demonstrated that the 21-gene recurrence score can be used to guide adjuvant systemic therapy decisions in postmenopausal women with pN1 ER+/HER2- breast cancer. As such, a sentinel lymph node biopsy (SLNB) may not provide systemic treatment-altering information for many patients, and omission of SLNB in patients with low probability of pN2/N3 disease could be considered.

methodsPostmenopausal women (aged ≥ 50 years) diagnosed with cN0cM0, ER+/HER- breast cancer from 2013 to 2017 were identified in the National Cancer Database. The primary outcome was the prevalence of pN2/N3 disease.

resultsOf 325,692 postmenopausal women with cN0 ER+/HER2- breast cancer, 7106 (2.2%) were pN2/N3. In total, 81.7% had cT1 tumors, 16.8% T2, 1.3% T3, and 0.2% T4. In patients with T1 tumors, the prevalence of pN2/N3 disease was 1.2% compared with 17.2% in patients with T3/T4 tumors. In multivariable models, cT stage was the strongest predictor of pN2/N3 disease (adjusted odds ratio [aOR] 14.9 [12.1-18.4]). Lobular histology (aOR 2.4 [2.3-2.6]), higher grade (aOR 2.9 [2.6-3.1]), and young age (aOR 1.5 [1.3-1.7]) were also associated with increased prevalence of pN2/N3. We created a model using histology, grade, and T stage that stratifies patients with low prevalence of pN2/3 disease (< 1%) and those at high risk (> 20%).

conclusionsIn postmenopausal women with cN0 ER+/HER2- breast cancer, the prevalence of pN2/N3 disease is low, indicating a potential opportunity to use the results of RxPONDER to extend criteria to omit SLNB. Prospective study is needed to determine safety, including risk of nodal recurrence, of omission of SLNB in carefully selected patients.

Indexed as

Breast NeoplasmsAxillaCombined Modality TherapyFemaleHumansLymph Node ExcisionNeoplasm StagingPostmenopausePrevalenceSentinel Lymph Node Biopsy

Identifiers

PMID35752724
PMCPMC9561012
OpenAlexW4283449152

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.