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dc.contributor.author | Jantus Lewintre, Eloisa | es_ES |
dc.contributor.author | Sanmartin, Elena | es_ES |
dc.contributor.author | Sirera Pérez, Rafael | es_ES |
dc.contributor.author | Blasco, Ana | es_ES |
dc.contributor.author | Sanchez, Jose Javier | es_ES |
dc.contributor.author | Taron, Miguel | es_ES |
dc.contributor.author | Rosell, Rafael | es_ES |
dc.contributor.author | Camps, Carlos | es_ES |
dc.date.accessioned | 2017-01-27T13:11:34Z | |
dc.date.available | 2017-01-27T13:11:34Z | |
dc.date.issued | 2011-11 | |
dc.identifier.issn | 0169-5002 | |
dc.identifier.uri | http://hdl.handle.net/10251/77412 | |
dc.description.abstract | Introduction: The vascular endothelial growth factor (VEGF) family of ligands and receptors (VEGFR) play an important role in tumor angiogenesis. Increased expression of angiogenic factors in tumors or in blood is associated with poor prognosis. The aim of this study was to investigate the role of VEGF-A and soluble VEGFR-2 (sVEGFR-2) as biomarkers in advanced non-small-cell lung cancer (NSCLC). Methods: We studied 432 patients with advanced NSCLC (stages IIIB-IV) treated with cisplatin and docetaxel and 89 healthy age-matched controls. Blood samples were collected before chemotherapy, and VEGF-A and sVEGFR-2 levels were determined by ELISA. Results: VEGF-A and sVEGFR-2 levels were higher in NSCLC patients than in the controls, but VEGF-A behaves as a better diagnostic biomarker. There were no significant associations between VEGF-A and sVEGFR-2 concentrations and clinical characteristics, such as ECOG-PS, gender, stage, histology, metastases, and treatment response. A patient subgroup characterized by a combination of high VEGF-A and low sVEGFR-2 levels exhibited the worst patient prognoses in terms of TTP and OS. Conclusions: VEGF-A and sVEGFR-2 levels were significantly higher in patients than in the controls. A combination of VEGF-A and sVEGFR-2 can be used as an independent prognostic biomarker in advanced NSCLC. © 2011 Elsevier Ireland Ltd. | es_ES |
dc.description.sponsorship | This work was supported in part, by a grant [PI06/104] from Instituto de Salud Carlos III and a grant [RD06/0020/1024] from Red Tematica de Investigacion Cooperativa en Cancer (RTICC), Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Science and Innovation and European Regional Development Fund (ERDF) "Una manera de hacer Europa". | en_EN |
dc.language | Inglés | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation | European Regional Development Fund (ERDF) "Una manera de hacer Europa" | es_ES |
dc.relation.ispartof | Lung Cancer | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Advanced NSCLC | es_ES |
dc.subject | Biomarkers | es_ES |
dc.subject | Prognostic | es_ES |
dc.subject | VEGF | es_ES |
dc.subject | VEGFR-2 | es_ES |
dc.subject | Cisplatin | es_ES |
dc.subject | Docetaxel | es_ES |
dc.subject | Vasculotropin A | es_ES |
dc.subject | Vasculotropin receptor 2 | es_ES |
dc.subject | Adult | es_ES |
dc.subject | Advanced cancer | es_ES |
dc.subject | Aged | es_ES |
dc.subject | Article | es_ES |
dc.subject | Cancer combination chemotherapy | es_ES |
dc.subject | Cancer diagnosis | es_ES |
dc.subject | Enzyme linked immunosorbent assay | es_ES |
dc.subject | Female | es_ES |
dc.subject | Human | es_ES |
dc.subject | Lung non small cell cancer | es_ES |
dc.subject | Major clinical study | es_ES |
dc.subject | Male | es_ES |
dc.subject | Priority journal | es_ES |
dc.subject | Prognosis | es_ES |
dc.subject | Aged, 80 and over | es_ES |
dc.subject | Antineoplastic Combined Chemotherapy Protocols | es_ES |
dc.subject | Carcinoma, Non-Small-Cell Lung | es_ES |
dc.subject | Disease Progression | es_ES |
dc.subject | Humans | es_ES |
dc.subject | Lung Neoplasms | es_ES |
dc.subject | Middle Aged | es_ES |
dc.subject | Neoplasm Staging | es_ES |
dc.subject | Taxoids | es_ES |
dc.subject | Tumor Markers, Biological | es_ES |
dc.subject | Vascular Endothelial Growth Factor A | es_ES |
dc.subject | Vascular Endothelial Growth Factor Receptor-2 | es_ES |
dc.subject.classification | MICROBIOLOGIA | es_ES |
dc.title | Combined VEGF-A and VEGFR-2 concentrations in plasma: diagnostic and prognostic implications in patients with advanced NSCLC | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1016/j.lungcan.2011.02.016 | |
dc.relation.projectID | info:eu-repo/grantAgreement/ISCIII//PI06%2F104/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MSC//RD06%2F0020%2F1024/ES/RED TEMÁTICA DE INVESTIGACIÓN COOPERATIVA DEL CANCER/ | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural | es_ES |
dc.description.bibliographicCitation | Jantus Lewintre, E.; Sanmartin, E.; Sirera Pérez, R.; Blasco, A.; Sanchez, JJ.; Taron, M.; Rosell, R.... (2011). Combined VEGF-A and VEGFR-2 concentrations in plasma: diagnostic and prognostic implications in patients with advanced NSCLC. Lung Cancer. 74(2):326-331. https://doi.org/10.1016/j.lungcan.2011.02.016 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://dx.doi.org/10.1016/j.lungcan.2011.02.016 | es_ES |
dc.description.upvformatpinicio | 326 | es_ES |
dc.description.upvformatpfin | 331 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 74 | es_ES |
dc.description.issue | 2 | es_ES |
dc.relation.senia | 221012 | es_ES |
dc.contributor.funder | Instituto de Salud Carlos III | es_ES |
dc.contributor.funder | Ministerio de Sanidad y Consumo | es_ES |
dc.contributor.funder | European Regional Development Fund | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |