Evidence map›Paper›PMID 38918556›Full record

ArticleBritish journal of cancer2024

A non-invasive artificial intelligence model for identifying axillary pathological complete response to neoadjuvant chemotherapy in breast cancer: a secondary analysis to multicenter clinical trial.

Teng Zhu, Yu-Hong Huang, Wei Li, Can-Gui Wu, Yi-Min Zhang, Xing-Xing Zheng, Ting-Feng Zhang, Ying-Yi Lin, Zai-Yi Liu, Guo-Lin Ye and 3 more

2 registry-linked trialsAbstract readMulticenter Study
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT03154749 phase2completednot on this map

Neoadjuvant Docetaxel + Carboplatin Versus Epirubicin+Cyclophosphamide Followed by Docetaxel in Triple-Negative, Early-Stage Breast Cancer (NeoCART): Study Protocol for a Multicenter, Randomized Controlled, Open-Label, Phase 2 Trial

TypeinterventionalSponsorGuangdong Provincial People's HospitalRan2016 to 2019Enrolled93ConditionsTriple-Negative Breast CancerArmsDCb (docetaxel/carboplatin) versus EC followed by D (epirubicin/cyclophosphamide followed by docetaxe)
NCT04858529 phase3unknown statusnot on this map

Neoadjuvant TCHP Versus THP in Patients With Human Epidermal Growth Factor Receptor 2-positive Breast Cancer (neoCARHP) : a Randomized, Open-label, Multicenter, Phase III Trial

TypeinterventionalSponsorGuangdong Provincial People's HospitalRan2021 to 2025Enrolled774ConditionsNeoadjuvant Therapies for HER2+ Breast CancerArmsinvestigator-selected taxane/carboplatin/trastuzumab/pertuzumab (TCHP), investigator-selected taxane/trastuzumab/pertuzumab (THP)
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Article
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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

13 authors.

Teng Zhu *Department of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Yu-Hong Huang *Department of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Wei Li *The Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Can-Gui Wu *Department of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Yi-Min ZhangDiagnosis and Treatment Center of Breast Diseases, Shantou Central Hospital, Shantou, China.
Xing-Xing ZhengDepartment of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Ting-Feng ZhangDepartment of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Ying-Yi LinDepartment of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Zai-Yi LiuDepartment of Radiology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, Guangdong, China.
Guo-Lin YeDepartment of Breast Cancer, The First People's Hospital of Foshan, Foshan, Guangdong, China.
Ying LinBreast Disease Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.ORCID http://orcid.org/0000-0002-5923-3306
Zhi-Yong WuDiagnosis and Treatment Center of Breast Diseases, Shantou Central Hospital, Shantou, China. stwuzy@163.com.
Kun WangDepartment of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China. gzwangkun@126.com.ORCID http://orcid.org/0000-0001-9851-7080

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82171898
6 · The paper itself

Abstract

backgroundThis study aims to develop a stacking model for accurately predicting axillary lymph node (ALN) response to neoadjuvant chemotherapy (NAC) using longitudinal MRI in breast cancer.

methodsWe included patients with node-positive breast cancer who received NAC following surgery from January 2012 to June 2022. We collected MRIs before and after NAC, and extracted radiomics features from the tumour, peritumour, and ALN regions. The Mann-Whitney U test, least absolute shrinkage and selection operator, and Boruta algorithm were used to select features. We utilised machine learning techniques to develop three single-modality models and a stacking model for predicting ALN response to NAC.

resultsThis study consisted of a training cohort (n = 277), three external validation cohorts (n = 313, 164, and 318), and a prospective cohort (n = 81). Among the 1153 patients, 60.62% achieved ypN0. The stacking model achieved excellent AUCs of 0.926, 0.874, and 0.862 in the training, external validation, and prospective cohort, respectively. It also showed lower false-negative rates (FNRs) compared to radiologists, with rates of 14.40%, 20.85%, and 18.18% (radiologists: 40.80%, 50.49%, and 63.64%) in three cohorts. Additionally, there was a significant difference in disease-free survival between high-risk and low-risk groups (p < 0.05).

conclusionsThe stacking model can accurately predict ALN status after NAC in breast cancer, showing a lower false-negative rate than radiologists. TRIAL REGISTRATION NUMBER: The clinical trial numbers were NCT03154749 and NCT04858529.

Indexed as

Artificial IntelligenceAxillaBreast NeoplasmsMagnetic Resonance ImagingNeoadjuvant TherapyAdultAgedChemotherapy, AdjuvantFemaleHumansLymphatic MetastasisLymph NodesMachine LearningMiddle AgedProspective Studies

Identifiers

PMID38918556
PMCPMC11333754

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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 Socratic graph.