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               <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>
               <dc:description>COVID-19; SARS-CoV-2; Multiple myeloma</dc:description>
               <dc:description>COVID-19; SARS-CoV-2; Mieloma múltiple</dc:description>
               <dc:description>COVID-19; SARS-CoV-2; Mieloma múltiple</dc:description>
               <dc:description>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.</dc:description>
               <dc:description>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).</dc:description>
               <dc:date>2024-06-06T08:42:13Z</dc:date>
               <dc:date>2024-06-06T08:42:13Z</dc:date>
               <dc:date>2024-02-01T11:40:03Z</dc:date>
               <dc:date>2024-02-01T11:40:03Z</dc:date>
               <dc:date>2024-01</dc:date>
               <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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