<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-14T03:39:41Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/15880" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/15880</identifier><datestamp>2025-05-05T10:08:49Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19616</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Martín-Carrasco, Clara</subfield>
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      <subfield code="a">Delgado-Bonet, Pablo</subfield>
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      <subfield code="a">Tomeo-Martín, Beatriz Davinia</subfield>
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      <subfield code="a">Pastor, Josep</subfield>
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      <subfield code="a">de la Riva, Claudia</subfield>
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      <subfield code="a">Palau-Concejo, Paula</subfield>
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      <subfield code="a">Del Castillo, Noemí</subfield>
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      <subfield code="a">Garcia-Castro, Javier</subfield>
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      <subfield code="a">Perise-Barrios, Ana Judith</subfield>
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      <subfield code="c">2022-06-28</subfield>
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      <subfield code="a">The use of oncolytic viruses is an innovative approach to lyse tumor cells and induce antitumor immune responses. Eight dogs diagnosed with carcinoma/adenocarcinoma were intratumorally treated with ICOCAV15, an oncolytic canine adenovirus (CAV). To evaluate the treatment's safety, a blood count, biochemistry, and coagulation test were performed before treatment and during follow-up. Immune populations were analyzed by flow cytometry. Anti-adenovirus antibodies were also determined. The immune infiltration, vascularization, and viral presence in the tumor were determined by CD3, CD4, CD20, CD31 and CAV by immunohistochemistry. All the dogs maintained a good quality of life during follow-up, and some had increased median survival time when compared with dogs treated with chemotherapy. No treatment-related adverse effects were detected. The Response Evaluation Criteria In Solid Tumors criteria were also assessed: two patients showed a partial response and the rest showed stable disease at various times during the study. ICOCAV15 was detected inside the tumor during follow-up, and antiviral antibodies were detected in all patients. Furthermore, the tumor-infiltrating immune cells increased after viral administration. Therefore, we suggest that intratumorally administered ICOCAV15 could represent as a new tool for the treatment of canine carcinoma because it is safe, well-tolerated by dogs, and shows promising results.</subfield>
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      <subfield code="a">Vet Sci. 2022 Jun 28;9(7):327.</subfield>
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      <subfield code="a">10.3390/vetsci9070327</subfield>
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      <subfield code="a">Veterinary sciences</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/15880</subfield>
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      <subfield code="a">Oncolytic Viruses</subfield>
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      <subfield code="a">Canine carcinoma</subfield>
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      <subfield code="a">Safety and Efficacy of an Oncolytic Adenovirus as an Immunotherapy for Canine Cancer Patients</subfield>
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