<?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>2026-04-13T01:27:40Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/467062" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/467062</identifier><datestamp>2025-11-09T09:46:30Z</datestamp><setSpec>com_2072_98</setSpec><setSpec>col_2072_378192</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Varona, Jose F.</subfield>
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      <subfield code="a">Landete, Pedro</subfield>
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      <subfield code="a">Paredes, Roger</subfield>
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      <subfield code="a">Vates, Roberto</subfield>
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      <subfield code="a">Torralba, Miguel</subfield>
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      <subfield code="a">Guisado-Vasco, Pablo</subfield>
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      <subfield code="a">Porras, Lourdes</subfield>
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      <subfield code="a">Munoz, Patricia</subfield>
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      <subfield code="a">Gijon, Paloma</subfield>
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      <subfield code="a">Ancochea, Julio</subfield>
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      <subfield code="a">Saiz, Elena</subfield>
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      <subfield code="a">Meira, Fernanda</subfield>
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      <subfield code="a">Jimeno, Jose M..</subfield>
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      <subfield code="a">Lopez-Martin, Jose A.</subfield>
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      <subfield code="a">Estrada, Vicente</subfield>
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      <subfield code="a">Universitat Autònoma de Barcelona</subfield>
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      <subfield code="c">2023</subfield>
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      <subfield code="a">The APLICOV-PC study assessed the safety and preliminary efficacy of plitidepsin in hospitalized adult patients with COVID-19. In this follow-up study (E-APLICOV), the incidence of post-COVID-19 morbidity was evaluated and any long-term complications were characterized. Between January 18 and March 16, 2022, 34 of the 45 adult patients who received therapy with plitidepsin in the APLICOV-PC study were enrolled in E-APLICOV (median time from plitidepsin first dose to E-APLICOV enrollment, 16.8 months [range, 15.2-19.5 months]). All patients were functionally autonomous with regard to daily living (Barthel index: 100) and had normal physical examinations. From the APLICOV-PC date of discharge to the date of the extension visit, neither Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5) grade 3-4 complications nor QT prolongation or significant electrocardiogram (EKG) abnormalities were reported. Five (14.7%) patients had another COVID-19 episode after initial discharge from APLICOV-PC, and in 2 patients (5.9%), previously unreported chest X-ray findings were documented. Spirometry and lung-diffusion tests were normal in 29 (85.3%) and 27 (79.4%) patients, respectively, and 3 patients needed additional oxygen supplementation after initial hospital discharge. None of these patients required subsequent hospital readmission for disease-related complications. In conclusion, plitidepsin has demonstrated a favorable long-term safety profile in adult patients hospitalized for COVID-19. With the constraints of a low sample size and a lack of control, the rate of post-COVID-19 complications after treatment with plitidepsin is in the low range of published reports. (ClinicalTrials.gov Identifier: NCT05121740;).</subfield>
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      <subfield code="a">Plitidepsin</subfield>
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      <subfield code="a">COVID-19</subfield>
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      <subfield code="a">SARS-CoV-2</subfield>
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      <subfield code="a">Long COVID</subfield>
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      <subfield code="a">Post-COVID-19 complications</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Plitidepsin in adult patients with COVID-19 requiring hospital admission : A long-term follow-up analysis</subfield>
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