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dc.contributor.authorCarmona-Bayonas, A.
dc.contributor.authorVerso, M.
dc.contributor.authorSánchez Cánovas, M.
dc.contributor.authorRubio Pérez, J.
dc.contributor.authorGarcía de Herreros, M.
dc.contributor.authorMartínez Del Prado, P.
dc.contributor.authorFernández Pérez, Isaura 
dc.contributor.authorQuintanar Verduguez, T.
dc.contributor.authorObispo Portero, B.
dc.contributor.authorPachón Olmos, V.
dc.contributor.authorGómez, D.
dc.contributor.authorOrtega, L.
dc.contributor.authorSerrano Moyano, M.
dc.contributor.authorM Brozos, E.
dc.contributor.authorBiosca, M.
dc.contributor.authorAntonio Rebollo, M.
dc.contributor.authorTeijeira Sanchez, L.
dc.contributor.authorHernández Pérez, C.
dc.contributor.authorDavid Cumplido Burón, J.
dc.contributor.authorMartinez Lago, Nieves Purificacion 
dc.contributor.authorGarcía Pérez, E.
dc.contributor.authorMuñoz Langa, J.
dc.contributor.authorPérez Segura, P.
dc.contributor.authorMartínez de Castro, E.
dc.contributor.authorJimenez-Fonseca, P.
dc.contributor.authorAgnelli, G.
dc.contributor.authorMuñoz, A.
dc.date.accessioned2025-08-26T11:13:44Z
dc.date.available2025-08-26T11:13:44Z
dc.date.issued2022
dc.identifier.citationCarmona-Bayonas A, Verso M, Sánchez Cánovas M, Rubio Pérez J, García de Herreros M, Martínez Del Prado P, et al. Do Antiangiogenics Promote Clot Instability? Data from the TESEO Prospective Registry and Caravaggio Clinical Trial. Thrombosis and haemostasis. 2022;122(10):1653-61.
dc.identifier.issn2567-689X
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/634ee01948ee3619a115c0e3*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20868
dc.description.abstractBACKGROUND: Venous thromboembolism (VTE) is a common complication in cancer patients. Much of its morbidity stems from the development of fatal pulmonary embolisms (PE). Little is known about the factors involved in clot stability, with angiogenesis possibly being implicated. METHODS: The database is from the TESEO prospective registry that recruits cancer patients with VTE from 41 Spanish hospitals. Independent validation was conducted in a cohort from the Caravaggio trial. The objective is to evaluate the association between exposure to antiangiogenic therapies and the PE/VTE proportion in oncological patients. RESULTS: In total, 1,536 subjects were evaluated; 58.4% (n = 894) had a PE and 7% (n = 108) received antiangiogenic therapy (bevacizumab in 75%). The PE/VTE proportion among antiangiogenic-treated individuals was 77/108 (71.3%) versus 817/1,428 (57.2%) among those receiving other alternative therapies (p = 0.004). The effect of the antiangiogenics on the PE/VTE proportion held up across all subgroups except for active smokers or those with chronic obstructive pulmonary disease. Exposure to antiangiogenics was associated with increased PEs, odds ratio (OR) 2.27 (95% CI, 1.42-3.63). In the Caravaggio trial, PE was present in 67% of the individuals treated with antiangiogenics, 50% of those who received chemotherapy without antiangiogenic treatment, and 60% without active therapy (p = 0.0016). CONCLUSION: Antiangiogenics are associated with increased proportion of PE in oncological patients with VTE. If an effect on clot stability is confirmed, the concept of thrombotic risk in cancer patients should be reconsidered in qualitative terms.en
dc.description.sponsorshipThis study was supported by unrestricted grants from Sanofi, Leo Pharma Rovi, and BMS-Pfizer. The sponsors of this research have not participated in data collection, analysis, or interpretation, in writing the report, or in the decision to submit the article for publication.en
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleDo Antiangiogenics Promote Clot Instability? Data from the TESEO Prospective Registry and Caravaggio Clinical Trial*
dc.typeArticleen
dc.authorsophosCarmona-Bayonas, A. A.
dc.authorsophosVerso, M.
dc.authorsophosSánchez Cánovas, M.
dc.authorsophosRubio Pérez, J.
dc.authorsophosGarcía de Herreros, M.
dc.authorsophosMartínez Del Prado, P.
dc.authorsophosFernández Pérez, I.
dc.authorsophosQuintanar Verduguez, T.
dc.authorsophosObispo Portero, B.
dc.authorsophosPachón Olmos, V.
dc.authorsophosGómez, D.
dc.authorsophosOrtega, L.
dc.authorsophosSerrano Moyano, M.
dc.authorsophosM Brozos, E.
dc.authorsophosBiosca, M.
dc.authorsophosAntonio Rebollo, M.
dc.authorsophosTeijeira Sanchez, L.
dc.authorsophosHernández Pérez, C.
dc.authorsophosDavid Cumplido Burón, J.
dc.authorsophosMartínez Lago, N.
dc.authorsophosGarcía Pérez, E.
dc.authorsophosMuñoz Langa, J.
dc.authorsophosPérez Segura, P.
dc.authorsophosMartínez de Castro, E.
dc.authorsophosJimenez-Fonseca, P.
dc.authorsophosAgnelli, G.
dc.authorsophosMuñoz
dc.identifier.doi10.1055/a-1816-8347
dc.identifier.sophos634ee01948ee3619a115c0e3
dc.issue.number10
dc.journal.titleThrombosis and haemostasis*
dc.page.initial1653
dc.page.final1661
dc.relation.projectIDSanofi; Leo Pharma Rovi; BMS-Pfizer
dc.relation.publisherversionhttp://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1816-8347.pdf;https://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1816-8347.pdfes
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Vigoes
dc.subject.keywordCHUVIes
dc.subject.keywordIISGSes
dc.subject.keywordAS Ferroles
dc.subject.keywordCHUFes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number122


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