<?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>2026-07-21T14:19:55Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/14957" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/14957</identifier><datestamp>2025-06-18T07:04:59Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_2052</setSpec><setSpec>col_20.500.12105_16962</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">Ruano, David</subfield>
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      <subfield code="a">López-Martín, José A</subfield>
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      <subfield code="a">Lassaletta, Álvaro</subfield>
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      <subfield code="a">Bautista, Francisco</subfield>
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      <subfield code="a">Andión, Maitane</subfield>
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      <subfield code="a">Hernández, Carmen</subfield>
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      <subfield code="a">González-Murillo, África</subfield>
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      <subfield code="a">Melen, Gustavo</subfield>
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      <subfield code="a">Alemany, Ramón</subfield>
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      <subfield code="a">Madero, Luis</subfield>
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      <subfield code="a">Garcia-Castro, Javier</subfield>
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      <subfield code="a">Ramírez, Manuel</subfield>
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      <subfield code="c">2020-04-08</subfield>
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      <subfield code="a">We present here the results of a first-in-human, first-in-child trial for patients with relapsed/refractory solid tumors using Celyvir, an advanced therapy medicine that combines autologous mesenchymal stem cells (MSCs) carrying an oncolytic adenovirus. Celyvir was manufactured from a bone marrow aspirate and then given intravenously. Patients received weekly infusions for 6 weeks at a dose of 2 × 106 cells/kg (children) or 0.5-1 × 106 cells/kg (adults), 2 × 104 viral particles per cell. Fifteen pediatric and 19 adult patients were recruited, but 18 were screen failures, mainly because rapid disease progression before Celyvir was available. No grade 2-5 toxicities were reported. Adenoviral replication detected by PCR was found in all but 2 pediatric patient and in none of the adult ones. Absolute numbers of circulating leukocytes suffered minor changes along therapy, but some subsets showed differences comparing the pediatric versus the adult cohorts. Two patients with neuroblastoma showed disease stabilization, and one of them continued on treatment for up to 6 additional weeks. Celyvir, the combination of MSCs and oncolytic adenovirus, is safe and warrants further evaluation in a phase 2 setting. The use of MSCs may be a strategy to increase the amount of oncolytic virus administered to patients, minimizing toxicities and avoiding direct tumor injections.</subfield>
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      <subfield code="a">Mol Ther. 2020 Apr 8;28(4):1033-1042.</subfield>
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      <subfield code="a">10.1016/j.ymthe.2020.01.019</subfield>
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      <subfield code="a">1525-0024</subfield>
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      <subfield code="a">Molecular therapy : the journal of the American Society of Gene Therapy</subfield>
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      <subfield code="a">32053771</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/14957</subfield>
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      <subfield code="a">Clinical trial</subfield>
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      <subfield code="a">Mesenchymal stem cells</subfield>
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      <subfield code="a">Oncolytic virotherapy</subfield>
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      <subfield code="a">First-in-Human, First-in-Child Trial of Autologous MSCs Carrying the Oncolytic Virus Icovir-5 in Patients with Advanced Tumors</subfield>
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