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dc.contributor.authorARIAS RON, DAVID 
dc.contributor.authorLABANDEIRA GUERRA, CARMEN MARIA 
dc.contributor.authorAreses Manrique, María Carmen 
dc.contributor.authorSAMPEDRO DOMARCO, PAULA 
dc.contributor.authorAbdulkader Nallib, Ihab 
dc.contributor.authorGarcía Mata, Jesús 
dc.contributor.authorRolfo, C.
dc.contributor.authorGonzalez-Rivas, D.
dc.contributor.authorFirvida Perez, Jose Luis 
dc.date.accessioned2021-11-23T09:13:58Z
dc.date.available2021-11-23T09:13:58Z
dc.date.issued2019
dc.identifier.issn2234-943X
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743439/pdf/fonc-09-00819.pdfes]bi
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31552167es]bi
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15725
dc.description.abstractIn a patient who had been diagnosed of located squamous cell lung carcinoma, pneumonectomy, and adjuvant chemotherapy were performed. Brain recurrence and subsequent lung metastatic disease were uncontrolled by neurosurgery, holocranial radiotherapy, and first-line chemotherapy. In August 2015, appearance of leptomeningeal carcinomatosis triggered severe clinical deterioration and threatened the patient's life. Anti-PD1 immune checkpoint inhibitor Nivolumab was initiated in an attempt to stop tumor growth, achieving a spectacular brain and pulmonary complete response and clinical improvement, without serious adverse effects. High expression PD-L1 level (100%) was found in the pathological tissue sample. Nivolumab was maintained for more than 2 years and stopped in December 2017 after 28 months of treatment, with no disease evidence. More than 3 years after its onset, the patient maintains an outstanding PS with complete tumor response and no evidence of disease in last surveillance CT scan and brain MRI.es
dc.language.isoenges
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleDramatic Response of Leptomeningeal Carcinomatosis to Nivolumab in PD-L1 Highly Expressive Non-small Cell Lung Cancer: A Case Reportes
dc.typeArtigoes
dc.authorsophosRon, D. A.
dc.authorsophosLabandeira, C. M.
dc.authorsophosManrique, M. C. A.
dc.authorsophosDomarco, P. S.
dc.authorsophosAbdulkader, I.
dc.authorsophosGarcia-Mata, J.
dc.authorsophosRolfo, C.
dc.authorsophosGonzalez-Rivas, D.
dc.authorsophosFirvida, J. L.
dc.identifier.doi10.3389/fonc.2019.00819
dc.identifier.pmid31552167
dc.identifier.sophos31472
dc.issue.number-es
dc.journal.titleFRONTIERS IN ONCOLOGYes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Anatomía Patolóxicaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Complexo Hospitalario Universitario de Ourense::Oncoloxía médicaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Vigo - Complexo Hospitalario Universitario de Vigo::Neuroloxíaes
dc.rights.accessRightsopenAccesses
dc.subject.keywordCHUSes
dc.subject.keywordCHUOes
dc.subject.keywordCHUVIes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number9es


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Atribución 4.0 Internacional
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