Evidence map›Paper›PMID 40986210›Full record

ArticleAnnals of surgical oncology2026

Contemporary Trends in Axillary Surgery for ER-Positive, HER2-Negative Breast Cancer Stratified by Neoadjuvant Endocrine Therapy, Neoadjuvant Chemotherapy, or Upfront Surgery.

Sasha R Douglas, Samantha M Thomas, Akiko Chiba, Maggie L DiNome, Gayle A DiLalla, E Shelley Hwang, Kendra Modell Parrish, Laura H Rosenberger, Jennifer K Plichta, Ton Wang and 1 more

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2026. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

11 authors.

Sasha R DouglasDepartment of Surgery, Duke University, Durham, NC, USA.
Samantha M ThomasBiostatistics and Bioinformatics, Duke University, Durham, NC, USA.
Akiko ChibaDepartment of Surgery, Duke University, Durham, NC, USA.
Maggie L DiNomeDepartment of Surgery, Duke University, Durham, NC, USA.
Gayle A DiLallaDepartment of Surgery, Duke University, Durham, NC, USA.
E Shelley HwangDepartment of Surgery, Duke University, Durham, NC, USA.
Kendra Modell ParrishDepartment of Surgery, Duke University, Durham, NC, USA.
Laura H RosenbergerDepartment of Surgery, Duke University, Durham, NC, USA.
Jennifer K PlichtaDepartment of Surgery, Duke University, Durham, NC, USA.
Ton WangDepartment of Surgery, Duke University, Durham, NC, USA.
Astrid M Botty van den BrueleDepartment of Surgery, Duke University, Durham, NC, USA. Astrid.botty.van.den.bruele@duke.edu.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
Building Interdisciplinary Research Careers in Women's Health (K12) - Administrative SupplementK12AR084231 · NIAMS · DUKE UNIVERSITY · PI Cindy Amundsen · 2023 to 2026
$2.5M
NCI NIH HHS P30 CA014236NIAMS NIH HHS K12 AR084231NIH HHS K12AR084231NIH HHS P30CA014236
6 · The paper itself

Abstract

backgroundDe-escalation of axillary surgery for hormone receptor-positive breast cancer has gained traction, but guidelines for axillary management after neoadjuvant endocrine therapy (NET) remain ill-defined.

methodsFemale patients age ≥50 years with clinical T1-4c, N0-1, ER+/HER2-<PUB4> breast cancer (2012-2021) were selected from the National Cancer Database (NCDB) and divided into three groups based on treatment: upfront surgery, neoadjuvant chemotherapy (NAC), or NET. Axillary surgery was categorized as no axillary surgery, sentinel lymph node biopsy (SLNB) alone, sentinel lymph node biopsy followed by axillary lymph node dissection (ALND), or ALND alone. Descriptive analysis and logistic regression were used to identify factors associated with ALND, and survival analysis was performed.

resultsThe inclusion criteria were met by 792,581 patients. The majority underwent surgery first (94.3 %), whereas 2.6 % received NAC and 3.1 % received NET. After adjustment, the odds of undergoing ALND were shown to be higher for those receiving NAC (odds ratio [OR], 1.18; 95 % confidence interval [CI], 1.12-1.24) or NET (OR, 1.10; 95 % CI, 1.05-1.14) than for those receiving surgery first (p < 0.001). The patients receiving NET were less likely to convert from cN+ to ypN0 (8.3 % vs NAC 19.6 %; p < 0.001), but they still were less likely to undergo ALND after SLNB. Overall survival was highest among the patients in the surgery-first group regardless of clinical nodal status (p < 0.001).

conclusionsAlthough the patients receiving NET had lower rates of nodal pathologic complete response, this did not translate to higher conversion to ALND after SLNB, suggesting that providers do not interpret residual nodal disease after NET the same way as after NAC.

Indexed as

Antineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsLymph Node ExcisionMastectomyNeoadjuvant TherapyAgedAxillaChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansMiddle AgedPrognosisReceptors, EstrogenAntineoplastic Agents, HormonalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID40986210
PMCPMC12619107

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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.