Evidence map›Paper›PMID 41572090›Full record

ArticleJournal of neuro-oncology2026

Individualized prediction of brain metastasis risk in patients with breast cancer.

Gino Cioffi, Kristin Waite, Ancha Baranova, Jill S Barnholtz-Sloan

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Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Gino CioffiSchool of Systems Biology, George Mason University, Fairfax, VA, USA. gino.cioffi@gmail.com.
Kristin WaiteWinship Cancer Institute, Emory University, 1701 Uppergate Drive, Atlanta, GA, 30322, USA.
Ancha BaranovaSchool of Systems Biology, George Mason University, Fairfax, VA, USA.
Jill S Barnholtz-SloanWinship Cancer Institute, Emory University, 1701 Uppergate Drive, Atlanta, GA, 30322, USA. jillbsloan@emory.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer patients have a high risk of brain and central nervous system metastases (BrM) and therefore have poor outcomes. This study aimed to assess the impact of clinico-genomic factors on BrM risk in breast cancer and develop validated nomograms for risk prediction.

methodsClinico-genomic data on breast cancer patients were obtained from the AACR GENIE Biopharma Collaborative. These data were split into training and testing sets by academic institution. Using the training set, risk of BrM was evaluated through multivariable Fine-Gray subdistribution hazard modeling, implementing LASSO penalization for feature selection. Prediction metrics were assessed internally on the training set through bootstrap-cross validation, and externally on the testing set. Calibration curves, AUC, and Brier scores were calculated to assess prediction and discrimination. A nomogram for 2-, 3.5-, and 5- year risk of BrM was constructed.

resultsSynchronous bone metastases, HER+/HR- breast cancer subtype, and TP53 alterations were selected as top predictors of BrM risk. The final multivariable model showed good discriminate capability at 2- (AUC: 68.7; Brier: 5.3), 3.5- (AUC: 65.9, Brier: 12.9), and 5-years (AUC 63.0, Brier: 17.4). This model was externally validated on the testing set and performed well at 2- (AUC 72.5; Brier: 10.5), 3.5- (AUC: 73.3; Brier 13.6), and 5-years (AUC: 74.9; Brier: 16.5).

conclusionsNomograms that calculate individualized BrM risk probabilities for patients with breast cancer can provide clinical utility informing patients and their health care team members on risk of BrM development. An interactive webtool for individualized BrM risk probabilities can be found here: https://gcioffi.shinyapps.io/BrCA_nomo_brm_risk/ .

Indexed as

Biomarkers, TumorBrain NeoplasmsBreast NeoplasmsNomogramsAdultAgedFemaleFollow-Up StudiesHumansMiddle AgedPrognosisRisk AssessmentRisk FactorsBiomarkers, TumorBrain metastasesBreast cancerCumulative incidenceGenomicNomogramRisk

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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.