Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/222243
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dc.contributor.authorSierra Rodero, Belén-
dc.contributor.authorMartínez Toledo, Cristina-
dc.contributor.authorNadal, Ernest-
dc.contributor.authorMolina Alejandre, Marta-
dc.contributor.authorGarcía Campelo, Rosario-
dc.contributor.authorGil González, Ángeles-
dc.contributor.authorMassuti, Bartomeu-
dc.contributor.authorGarcía Grande, Aránzazu-
dc.contributor.authorDómine, Manuel-
dc.contributor.authorInsa, Amelia-
dc.contributor.authorCastro Carpeño, Javier de-
dc.contributor.authorHuidobro Vence, Gerardo-
dc.contributor.authorMajem, Margarita-
dc.contributor.authorMartínez Martí, Alex-
dc.contributor.authorMegias Vazquez, Diego-
dc.contributor.authorLobato Alosnos, Daniel Ángel-
dc.contributor.authorCollazo-Lorduy, Ana-
dc.contributor.authorCalvo, Virginia-
dc.contributor.authorProvencio, Mariano-
dc.contributor.authorCruz Bermúdez, Alberto-
dc.date.accessioned2025-07-15T08:24:37Z-
dc.date.available2025-07-15T08:24:37Z-
dc.date.issued2025-06-05-
dc.identifier.issn2162-402X-
dc.identifier.urihttps://hdl.handle.net/2445/222243-
dc.description.abstractPerioperative chemoimmunotherapy has significantly improved survival rates for non-small cell lung cancer (NSCLC). However, current tissue biomarkers remain inadequate, underscoring the need for more sensitive and accessible alternatives to monitor relapse risk. Intratumoral B-cells are increasingly recognized for their role in enhancing immunotherapy outcomes, yet the contribution of peripheral B-cells to immune surveillance remains unexplored. Peripheral B-cell immunophenotypes were analyzed from blood samples (at diagnosis, post-neoadjuvant, and at 6- and 12-months of adjuvant treatment) in 41 stage IIIA NSCLC patients treated with perioperative nivolumab plus chemotherapy, included in the NADIM clinical trial (NCT03081689). Results were correlated with 5-year survival outcomes and validated through unsupervised clustering. An increase in the percentage of total B-cells (CD19+CD20+) and na & iuml;ve B-cells (CD19+CD20+CD24+CD38+CD27-CD10-), along with a reduction in CD20 expression on total B-cells, a decrease in the proportion of memory B-cells (CD19+CD20+CD24+CD38-/lowCD27+) and transitional B-cells (CD19+CD20+CD24++CD38++CD10+), was observed during the time encompassed between the end of neoadjuvant treatment and the posterior 6 months of adjuvant treatment. Higher levels of CD20 expression on total B-cells, along with an increased percentage of memory B-cells, or activated B-cells (CD19+CD20+CD25+), at 6- and 12-months of adjuvant treatment, were associated with increased survival. Conversely, higher levels of a newly described circulating population of CD19+CD20lowCD25lowCD27low B-cells during adjuvant treatment were linked to disease progression. Perioperative nivolumab plus chemotherapy in resectable NSCLC patients induces significant changes in peripheral B-cells. The persistence of circulating memory B-cells during adjuvant treatment might play a crucial role in survival.-
dc.format.extent14 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherInforma UK Limited-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1080/2162402X.2025.2513109-
dc.relation.ispartofOncoImmunology, 2025, vol. 14, num. 1-
dc.relation.urihttps://doi.org/10.1080/2162402X.2025.2513109-
dc.rightscc-by-nc (c) Sierra Rodero, Belén et al., 2025-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationCèl·lules B-
dc.subject.classificationImmunoteràpia-
dc.subject.otherB cells-
dc.subject.otherImmunotheraphy-
dc.titlePeripheral memory B cell population maintenance and long-term survival after perioperative chemoimmunotherapy in NSCLC (NADIM trial)-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2025-07-10T13:42:52Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid40468805-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))



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