<?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>2026-04-13T01:22:34Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/10952" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/10952</identifier><datestamp>2024-06-06T08:42:13Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" 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://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Survival in multiple myeloma and SARS-COV-2 infection through the COVID-19 pandemic: Results from the EPICOVIDEHA registry</dc:title>
   <dc:creator>Musto, Pellegrino</dc:creator>
   <dc:creator>Sgherza, Nicola</dc:creator>
   <dc:creator>Bergantim, Rui</dc:creator>
   <dc:creator>Farina, Francesca</dc:creator>
   <dc:creator>Glenthøj, Andreas</dc:creator>
   <dc:creator>Salmanton-García, Jon</dc:creator>
   <dc:creator>Jiménez, Moraima</dc:creator>
   <dc:subject>COVID-19 (Malaltia)</dc:subject>
   <dc:subject>Mieloma múltiple</dc:subject>
   <dc:subject>DISEASES::Virus Diseases::RNA Virus Infections::Nidovirales Infections::Coronaviridae Infections::Coronavirus Infections</dc:subject>
   <dc:subject>DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Plasma Cell::Multiple Myeloma</dc:subject>
   <dc:subject>ENFERMEDADES::virosis::infecciones por virus ARN::infecciones por Nidovirales::infecciones por Coronaviridae::infecciones por Coronavirus</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células plasmáticas::mieloma múltiple</dc:subject>
   <dcterms:abstract>COVID-19; SARS-CoV-2; Multiple myeloma</dcterms:abstract>
   <dcterms:abstract>COVID-19; SARS-CoV-2; Mieloma múltiple</dcterms:abstract>
   <dcterms:abstract>COVID-19; SARS-CoV-2; Mieloma múltiple</dcterms:abstract>
   <dcterms:abstract>Patients affected by multiple myeloma (MM) have an increased risk of severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection and subsequent coronavirus (20)19 disease (COVID-19)-related death. The changing epidemiological and therapeutic scenarios suggest that there has been an improvement in severity and survival of COVID-19 during the different waves of the pandemic in the general population, but this has not been investigated yet in MM patients. Here we analyzed a large cohort of 1221 patients with MM and confirmed SARS-CoV-2 infection observed between February 2020, and August 2022, in the EPICOVIDEHA registry from 132 centers around the world. Median follow-up was 52 days for the entire cohort and 83 days for survivors. Three-hundred and three patients died (24%) and COVID-19 was the primary reason for death of around 89% of them. Overall survival (OS) was significantly higher in vaccinated patients with both stable and active MM versus unvaccinated, while only a trend favoring vaccinated patients was observed in subjects with responsive MM. Vaccinated patients with at least 2 doses showed a better OS than those with one or no vaccine dose. Overall, according to pandemic waves, mortality rate decreased over time from 34% to 10%. In multivariable analysis, age, renal failure, active disease, hospital, and intensive care unit admission, were independently associated with a higher number of deaths, while a neutrophil count above 0.5 × 109/L was found to be protective. This data suggests that MM patients remain at risk of SARS-CoV-2 infection even in the vaccination era, but their clinical outcome, in terms of OS, has progressively improved throughout the different viral phases of the pandemic.</dcterms:abstract>
   <dcterms:abstract>EPICOVIDEHA has received funds from Optics COMMIT (COVID-19 Unmet Medical Needs and Associated Research Extension) COVID-19 RFP program by GILEAD Science, United States (Project 2020–8223).</dcterms:abstract>
   <dcterms:dateAccepted>2024-06-06T08:42:13Z</dcterms:dateAccepted>
   <dcterms:available>2024-06-06T08:42:13Z</dcterms:available>
   <dcterms:created>2024-06-06T08:42:13Z</dcterms:created>
   <dcterms:issued>2024-02-01T11:40:03Z</dcterms:issued>
   <dcterms:issued>2024-02-01T11:40:03Z</dcterms:issued>
   <dcterms:issued>2024-01</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/10952</dc:identifier>
   <dc:relation>Hematological Oncology;42(1)</dc:relation>
   <dc:relation>https://doi.org/10.1002/hon.3240</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Wiley</dc:publisher>
   <dc:source>Scientia</dc:source>
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