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dc.contributor.authorMuñoz, A.*
dc.contributor.authorAy, C.*
dc.contributor.authorGrilz, E.*
dc.contributor.authorLópez, S.*
dc.contributor.authorFont, C.*
dc.contributor.authorPachón, V.*
dc.contributor.authorCastellón, V.*
dc.contributor.authorMartínez-Marín, V.*
dc.contributor.authorSalgado Fernández, Mercedes *
dc.contributor.authorMartínez, E.*
dc.contributor.authorCalzas, J.*
dc.contributor.authorOrtega, L.*
dc.contributor.authorRupérez, A.*
dc.contributor.authorSalas, E.*
dc.contributor.authorPabinger, I.*
dc.contributor.authorSoria, J.M.*
dc.date.accessioned2025-09-05T08:17:50Z
dc.date.available2025-09-05T08:17:50Z
dc.date.issued2023
dc.identifier.citationMuñoz A, Ay C, Grilz E, López S, Font C, Pachón V, et al. A Clinical-Genetic Risk Score for Predicting Cancer-Associated Venous Thromboembolism: A Development and Validation Study Involving Two Independent Prospective Cohorts. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2023;41(16):2911-25.
dc.identifier.issn1527-7755
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/648600afa219857f1d788f9a
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20967
dc.description.abstractPURPOSE: Venous thromboembolism (VTE) is a leading cause of death among patients with cancer. The Khorana score was developed for assessing the risk of VTE in outpatients with cancer receiving chemotherapy, but its accuracy in identifying patients at high risk has been questioned. The aim of this study was to develop and validate a clinical-genetic score that improves the assessment of VTE risk in oncology outpatients within 6 months of diagnosis. METHODS: The new score was developed using the data of 364 outpatients belonging to the Spanish ONCOTHROMB 12-01 population. In this cohort, clinical data associated with the risk of VTE were collected at the time of diagnosis, including the Khorana score. These patients were also genotyped for the 51 genetic variants known to be associated with VTE. Multivariate logistic regression was performed to determine the weight of each genetic and clinical variable in relation to VTE risk, allowing a clinical-genetic risk score (the ONCOTHROMB score) to be developed. The Khorana and the ONCOTHROMB scores were then compared via the area under the receiver operating characteristic curve (AUC), calibration, and the number of patients needed to treat. The new score was then validated in a study of 263 patients in the Vienna Cancer and Thrombosis Study population. RESULTS: Nine genetic variants, tumor site, TNM stage, and a body mass index of > 25 kg/m2 were found to be associated with VTE and were used to build the ONCOTHROMB score, which better predicted the overall risk of VTE than did the Khorana score (AUC, 0.781 v 0.580; P < .001). Similar AUC results were recorded in the validation study the Vienna Cancer and Thrombosis Study cohort involving patients with the same type of tumor (AUC for the ONCOTHROMB score v the Khorana score: 0.686 v 0.577; P < .001) and with all type of tumors (AUC for the ONCOTHROMB score v the Khorana score: 0.720 v 0.561; P < .0001). CONCLUSION: The ONCOTHROMB score for VTE risk in outpatients with cancer, which takes into account both clinical and genetic variables, better identifies patients who might benefit from primary thromboprophylaxis than does the Khorana score.
dc.description.sponsorshipSupported by the SETH, SEOM, Asociacion ActivaTT por la Salud and FIS (PI/20/00325).
dc.languageeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshHumans *
dc.subject.meshVenous Thromboembolism *
dc.subject.meshProspective Studies *
dc.subject.meshAnticoagulants *
dc.subject.meshNeoplasms *
dc.subject.meshRisk Factors *
dc.subject.meshThrombosis *
dc.subject.meshRisk Assessment *
dc.titleA Clinical-Genetic Risk Score for Predicting Cancer-Associated Venous Thromboembolism: A Development and Validation Study Involving Two Independent Prospective Cohorts
dc.typeArtigo
dc.authorsophosMuñoz, A.; Ay, C.; Grilz, E.; López, S.; Font, C.; Pachón, V.; Castellón, V.; Martínez-Marín, V.; Salgado, M.; Martínez, E.; Calzas, J.; Ortega, L.; Rupérez, A.; Salas, E.; Pabinger, I.; Soria, J.M.
dc.identifier.doi10.1200/jco.22.00255
dc.identifier.sophos648600afa219857f1d788f9a
dc.issue.number16
dc.journal.titleJournal of clinical oncology : official journal of the American Society of Clinical Oncology*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Ourense::Oncoloxía médica
dc.page.initial2911
dc.page.final2925
dc.relation.projectIDSETH
dc.relation.projectIDSEOM
dc.relation.projectIDAsociacion ActivaTT por la Salud
dc.relation.projectIDFIS [PI/20/00325]
dc.relation.publisherversionhttps://doi.org/10.1200/jco.22.00255
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Ourense
dc.subject.keywordCHUO
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number41


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