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APA

Delgado Bonet, Pablo & Tomeo Martín, Beatriz Davinia & Delgado Bonet, Blanca & Sardón Ruiz, David & Torrado Carvajal, Angel & Mateo, Isidro & Perisé Barrios, Ana Judith .Intracranial Virotherapy for a Canine Hemangioma.

ISO 690

Delgado Bonet, Pablo & Tomeo Martín, Beatriz Davinia & Delgado Bonet, Blanca & Sardón Ruiz, David & Torrado Carvajal, Angel & Mateo, Isidro & Perisé Barrios, Ana Judith. Intracranial Virotherapy for a Canine Hemangioma.

https://hdl.handle.net/20.500.12080/32718
dc.contributor.author Delgado Bonet, Pablo
dc.contributor.author Tomeo Martín, Beatriz Davinia
dc.contributor.author Delgado Bonet, Blanca
dc.contributor.author Sardón Ruiz, David
dc.contributor.author Torrado Carvajal, Angel
dc.contributor.author Mateo, Isidro
dc.contributor.author Perisé Barrios, Ana Judith
dc.date.accessioned 2022-10-19T12:45:05Z
dc.date.available 2022-10-19T12:45:05Z
dc.date.created 2022-10-02
dc.identifier.uri https://hdl.handle.net/20.500.12080/32718
dc.description.abstract Abstract: Intracranial hemangiomas are rare neoplastic lesions in dogs that usually appear with lifethreatening symptoms. The treatment of choice is tumor resection; however, complete resection is rarely achieved. The patient¿s prognosis therefore usually worsens due to tumor progression, and adjuvant treatments are required to control the disease. Oncolytic viruses are an innovative approach that lyses the tumor cells and induces immune responses. Here, we report the intratumoral inoculation of ICOCAV15 (an oncolytic adenovirus) in a canine intracranial hemangioma, as adjuvant treatment for incomplete tumor resection. The canine patient showed no side effects, and the tumor volume decreased over the 12 months after the treatment, as measured by magnetic resonance imaging using volumetric criteria. When progressive disease was detected at month 18, a new dose of ICOCAV15 was administered. The patient died 31.9 months after the first inoculation of the oncolytic adenovirus. Furthermore, tumor-infiltrated immune cells increased in number after the viral administrations, suggesting tumor microenvironment activation. The increased number of infiltrated immune cells, the long survival time and the absence of side effects suggest that ICOCAV15 could be a safe and effective treatment and should be further explored as a novel therapy for canine hemangiomas. Keywords: ICOCAV15; oncolytic adenovirus; virotherapy; immunotherapy; hemangioma; brain tumor; volumetric criteria es_ES
dc.format application/pdf es_ES
dc.language eng es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.title Intracranial Virotherapy for a Canine Hemangioma es_ES
dc.type info:eu-repo/semantics/article es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.location N/A es_ES


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