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pmid:30882627

Development of prognostic signature and nomogram for patients with breast cancer.

Jiao Su · Li-Feng Miao · Xiang-Hua Ye · Meng-Shen Cui · Xiao-Feng He

Medicine · 2019 doi:10.1097/MD.0000000000014617

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:30882627
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2026-11-01T15:40:43Z
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paper object · 10 fields
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title
Development of prognostic signature and nomogram for patients with breast cancer.
doi
10.1097/MD.0000000000014617
pmid
30882627
authors array · 5 items
[0]
Jiao Su
[1]
Li-Feng Miao
[2]
Xiang-Hua Ye
[3]
Meng-Shen Cui
[4]
Xiao-Feng He
journal
Medicine
year
2019
abstract
To identify prognostic signature that could predict the survival of patients with breast cancer (BC).Breast cancer samples and normal breast tissues in the TCGA-BRCA and GSE7390 were included. Differentially expressed genes (DEGs) were identified using the "limma" method. Overall survival (OS) associated with DEGs were obtained using univariate and multivariable Cox proportional-hazards regression analysis, and the corresponding prognostic signature and nomogram were constructed. Calibration analysis and decision curve analysis (DCA) were performed.In all, 742 DEGs were identified, 19 of which were independently correlated with the OS of BC patients. The OS of patients in the 19-gene signature low-risk group was significantly better than that in high-risk group (hazard ratio [HR] 0.3506, 95% confidence interval [CI] 0.2488-0.4939), and the 19-gene based signature was demonstrated to be an independent prognostic factor in patient with BC in the TCGA-BRCA cohort (HR 1.501, 95% CI 1.374-1.640) and validation cohort GSE7392 ((HR 0.3557, 95% CI 0.2155-0.5871, P < .0001)). The primary and internally validated C-indexes for the 19-gene signature-based nomogram were 0.817 and 8.013, respectively. The results of calibration analysis and DCA analysis confirmed the robustness and the clinical usability of the nomogram.We constructed a prognostic signature and nomogram for patient with BC, which showed good application prospect.
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Differentially expressed genes (DEGs) were identified using the “limma” method.
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sections[3] "Breast cancer gene expression study and differentially expressed genes (DEGs) between BC and normal breast tissue" paragraph 2
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The TCGA (The Cancer Genome Atlas) BC expression profile (The TCGA-BRCA cohort)[8] and the associated clinical information were downloaded from Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov/).
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title
Strong Time Dependence of the 76-Gene Prognostic Signature
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Breast cancer gene expression study and differentially expressed genes (DEGs) between BC and normal breast tissue
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Univariate and multivariable Cox proportional-hazards regression analysis on PFS and OS.
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The prognostic role of the 19-gene signature
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:30882627", "kind": "science-record", "revision": 9, "content_hash": "sha256:ff1f5342fd822c5d02321af0e544a6c02897db130de767f37a0cc1c1a7a317b2", "created_at": "2026-11-01T15:40:43Z", "updated_at": "2026-11-01T22:43:52Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development of prognostic signature and nomogram for patients with breast cancer.", "doi": "10.1097/MD.0000000000014617", "pmid": "30882627", "authors": ["Jiao Su", "Li-Feng Miao", "Xiang-Hua Ye", "Meng-Shen Cui", "Xiao-Feng He"], "journal": "Medicine", "year": 2019, "abstract": "To identify prognostic signature that could predict the survival of patients with breast cancer (BC).Breast cancer samples and normal breast tissues in the TCGA-BRCA and GSE7390 were included. Differentially expressed genes (DEGs) were identified using the \"limma\" method. Overall survival (OS) associated with DEGs were obtained using univariate and multivariable Cox proportional-hazards regression analysis, and the corresponding prognostic signature and nomogram were constructed. Calibration analysis and decision curve analysis (DCA) were performed.In all, 742 DEGs were identified, 19 of which were independently correlated with the OS of BC patients. The OS of patients in the 19-gene signature low-risk group was significantly better than that in high-risk group (hazard ratio [HR] 0.3506, 95% confidence interval [CI] 0.2488-0.4939), and the 19-gene based signature was demonstrated to be an independent prognostic factor in patient with BC in the TCGA-BRCA cohort (HR 1.501, 95% CI 1.374-1.640) and validation cohort GSE7392 ((HR 0.3557, 95% CI 0.2155-0.5871, P < .0001)). The primary and internally validated C-indexes for the 19-gene signature-based nomogram were 0.817 and 8.013, respectively. The results of calibration analysis and DCA analysis confirmed the robustness and the clinical usability of the nomogram.We constructed a prognostic signature and nomogram for patient with BC, which showed good application prospect.", "claims": [{"id": "claim-method", "statement": "Differentially expressed genes (DEGs) were identified using the “limma” method.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30882627", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Differentially expressed genes (DEGs) were identified using the “limma” method."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The TCGA (The Cancer Genome Atlas) BC expression profile (The TCGA-BRCA cohort)[8] and the associated clinical information were downloaded from Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30882627", "locator": "sections[3] \"Breast cancer gene expression study and differentially expressed genes (DEGs) between BC and normal breast tissue\" paragraph 2", "quote": "The TCGA (The Cancer Genome Atlas) BC expression profile (The TCGA-BRCA cohort)[8] and the associated clinical information were downloaded from Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov/)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:30882627"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE7390"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE7390"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:30882627", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1097/MD.0000000000014617", "sha256": 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