Evidence map›Paper›PMID 40349259›Full record

ArticleBreast cancer research and treatment2025

Survival outcomes after pathologic complete response with neoadjuvant endocrine therapy vs. neoadjuvant chemotherapy: a retrospective national database study.

Tori C Nierenberg, Samantha M Thomas, Ian Halliday, Astrid Botty van den Bruele, Akiko Chiba, Kendra J Modell Parrish, Hannah E Woriax, Maggie L DiNome, Kelly E Westbrook, Jennifer K Plichta

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Tori C NierenbergDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Samantha M ThomasDepartment of Biostatistics & Bioinformatics, Duke University, Durham, NC, USA.
Ian HallidayDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Astrid Botty van den BrueleDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Akiko ChibaDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Kendra J Modell ParrishDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Hannah E WoriaxDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Maggie L DiNomeDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Kelly E WestbrookDuke Cancer Institute, Durham, NC, USA.
Jennifer K PlichtaDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA. Jennifer.Plichta@duke.edu.ORCID http://orcid.org/0000-0002-7411-0558

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

backgroundNeoadjuvant therapies can result in pathologic complete response (pCR) in patients with breast cancer, which can be predictive of long-term outcomes. Patients with estrogen receptor positive (ER +) tumors may receive either neoadjuvant chemotherapy (NAC) or neoadjuvant endocrine therapy (NET). We sought to compare survival outcomes in those with non-metastatic ER + breast cancer who received NET or NAC and achieved pCR.

methodsAll patients diagnosed with ER + /HER2- stage I-III breast cancer, who received neoadjuvant systemic therapy followed by surgery, and achieved pCR, were selected from the National Cancer Database (NCDB, 2010-2021). The Kaplan-Meier method was used to estimate overall survival (OS), and log-rank tests were used to test for differences in OS. Cox Proportional Hazards models were used to estimate the association of NAC vs NET with OS, after adjustment for covariates.

results3313 patients met eligibility criteria: 3148 received NAC and 165 NET. The median follow-up for the entire cohort was 82 months (95% CI 80.4-83.1). Patients who received NAC were significantly younger (median age: NAC 49y vs NET 64y; p < 0.001), more likely to have a comorbidity score of 0 (NAC 89.3% vs NET 81.2%, p = 0.004), and more likely to have private insurance (NAC 68.9% vs NET 44.2%, p < 0.001). There were no significant differences between the NAC and NET patients based on race and ethnicity, income, education, or community type (all p > 0.05). The NAC treated patients were more likely to have larger tumors [median tumor size (IQR): NAC 3 cm (2.0-4.3) vs NET 1.3 cm (0.7-2.8); p < 0.001)], ductal histology (NAC 92.6% vs 81.2%, p < 0.001), and grade 3 tumors (NAC 70.2% vs 10.3%, p < 0.001). In the unadjusted Kaplan-Meier analysis, there was no significant difference in OS between NAC vs NET [5-year OS: NAC 0.935 vs NET 0.916; p = 0.08]. After adjustment for demographics, disease characteristics, and treatments, there remained no association between OS and study group (NAC vs NET; p = 0.63).

conclusionsPatients with ER + /HER2- early-stage breast cancer who achieved pCR had similar OS, regardless of whether they received NAC or NET. As such, pCR appears to have similar prognostic value irrespective of the type of systemic therapy used to obtain this favorable outcome.

Indexed as

Antineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsNeoadjuvant TherapyAdultAgedChemotherapy, AdjuvantDatabases, FactualErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedNeoplasm StagingPathologic Complete ResponseReceptors, EstrogenRetrospective StudiesAntineoplastic Agents, HormonalErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenBreast cancerChemotherapyEndocrine therapyEstrogen positive breast cancerNeoadjuvant therapyPathologic complete response

Identifiers

PMID40349259
PMCPMC12118946

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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.