Publication:
Multivariable clinical-genetic risk model for predicting venous thromboembolic events in patients with cancer.

dc.contributor.authorMuñoz Martín, Andrés J
dc.contributor.authorOrtega, Israel
dc.contributor.authorFont, Carme
dc.contributor.authorPachón, Vanesa
dc.contributor.authorCastellón, Victoria
dc.contributor.authorMartínez-Marín, Virginia
dc.contributor.authorSalgado, Mercedes
dc.contributor.authorMartínez, Eva
dc.contributor.authorCalzas, Julia
dc.contributor.authorRupérez, Ana
dc.contributor.authorSouto, Juan C
dc.contributor.authorMartín, Miguel
dc.contributor.authorSalas, Eduardo
dc.contributor.authorSoria, Jose M
dc.date.accessioned2023-01-25T10:05:42Z
dc.date.available2023-01-25T10:05:42Z
dc.date.issued2018-03-28
dc.description.abstractVenous thromboembolism (VTE) is a leading cause of death among patients with cancer. Outpatients with cancer should be periodically assessed for VTE risk, for which the Khorana score is commonly recommended. However, it has been questioned whether this tool is sufficiently accurate at identifying patients who should receive thromboprophylaxis. The present work proposes a new index, TiC-Onco risk score to be calculated at the time of diagnosis of cancer, that examines patients' clinical and genetic risk factors for thrombosis. We included 391 outpatients with a recent diagnosis of cancer and candidates for systemic outpatient chemotherapy. All were treated according to standard guidelines. The study population was monitored for 6 months, and VTEs were recorded. The Khorana and the TiC-Onco scores were calculated for each patient and their VTE predictive accuracy VTEs was compared. We recorded 71 VTEs. The TiC-Onco risk score was significantly better at predicting VTE than the Khorana score (AUC 0.73 vs. 0.58, sensitivity 49 vs. 22%, specificity 81 vs. 82%, PPV 37 vs. 22%, and NPV 88 vs. 82%). TiC-Onco risk score performed significantly better than Khorana score at identifying cancer patients at high risk of VTE who would benefit from personalised thromboprophylaxis.
dc.identifier.doi10.1038/s41416-018-0027-8
dc.identifier.essn1532-1827
dc.identifier.pmcPMC5931103
dc.identifier.pmid29588512
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931103/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41416-018-0027-8.pdf
dc.identifier.urihttp://hdl.handle.net/10668/12282
dc.issue.number8
dc.journal.titleBritish journal of cancer
dc.journal.titleabbreviationBr J Cancer
dc.language.isoen
dc.organizationHospital Torrecárdenas
dc.page.number1056-1061
dc.pubmedtypeJournal Article
dc.pubmedtypeObservational Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshChemoprevention
dc.subject.meshCohort Studies
dc.subject.meshFemale
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshModels, Genetic
dc.subject.meshMultivariate Analysis
dc.subject.meshNeoplasms
dc.subject.meshRisk Assessment
dc.subject.meshRisk Factors
dc.subject.meshSensitivity and Specificity
dc.subject.meshVenous Thromboembolism
dc.titleMultivariable clinical-genetic risk model for predicting venous thromboembolic events in patients with cancer.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number118
dspace.entity.typePublication

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