Evidence map›Paper›PMID 41310989›Full record

ArticleIET systems biology

A Neutrophil-Based Predictive Model for Axillary De-Escalation After Neoadjuvant Therapy in Node-Positive Breast Cancer.

Exian Mou, Rui Guo, Huaichao Luo, Jia Xu, Wen Wei

Abstract read
In one paragraph

Article in IET systems biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Exian MouDepartment of Plastic and Reconstructive Surgery, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, China.
Rui GuoDepartment of Plastic and Reconstructive Surgery, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, China.
Huaichao LuoDepartment of Clinical Laboratory, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.ORCID 0000-0002-8632-5230
Jia XuDepartment of Plastic and Reconstructive Surgery, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, China.
Wen WeiDepartment of Medical Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to develop a novel immunoscore system integrating peripheral blood immune signatures and clinical factors to predict axillary pathological complete response (apCR) in clinically node-positive (cN+) breast cancer patients after neoadjuvant treatment (NAT) and facilitate personalized axillary de-escalation strategies. A retrospective analysis was conducted on cN+ breast cancer patients who received NAT at Sichuan Cancer Hospital, with 437 cases (June 2018-June 2023) as the training set and 266 cases (July 2023-July 2024) as the validation set, where clinicopathological data and peripheral blood immune indices were collected, multivariate logistic regression was used to identify independent predictors of apCR, predictive models were compared via ROC analysis, and a nomogram was constructed based on the optimal model. The apCR rate was 48.7% (213/437), with multivariate analysis revealing HER2 positivity (OR = 6.32, 95% CI: 3.95-10.12, p < 0.001), clinical response (RECIST 1.1), and baseline neutrophil count (OR = 1.26 per unit increase, 95% CI: 1.08-1.48, p = 0.003) as independent predictors, while the combined clinical-hematologic model (AUC = 0.766) outperformed the clinical-only model (AUC = 0.757) with consistent performance in the validation cohort (AUC = 0.759) and baseline neutrophil count exhibiting a strong linear correlation with apCR rates (r = 0.97, p < 0.001). In conclusion, baseline neutrophil count, HER2 status, and clinical response jointly predict apCR post-NAT in cN+ breast cancer, and the proposed immunoscore nomogram offers a practical tool to guide axillary de-escalation and optimize surgical decision-making.

Indexed as

Breast NeoplasmsNeoadjuvant TherapyNeutrophilsAdultAgedAxillaFemaleHumansMiddle AgedNomogramsRetrospective StudiesbloodcancerPharmacologytoxicology

Identifiers

PMID41310989
PMCPMC12660155

What OpenQuestion holds

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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.