Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/222243
Title: Peripheral memory B cell population maintenance and long-term survival after perioperative chemoimmunotherapy in NSCLC (NADIM trial)
Author: Sierra Rodero, Belén
Martínez Toledo, Cristina
Nadal, Ernest
Molina Alejandre, Marta
García Campelo, Rosario
Gil González, Ángeles
Massuti, Bartomeu
García Grande, Aránzazu
Dómine, Manuel
Insa, Amelia
Castro Carpeño, Javier de
Huidobro Vence, Gerardo
Majem, Margarita
Martínez Martí, Alex
Megias Vazquez, Diego
Lobato Alosnos, Daniel Ángel
Collazo-Lorduy, Ana
Calvo, Virginia
Provencio, Mariano
Cruz Bermúdez, Alberto
Keywords: Cèl·lules B
Immunoteràpia
B cells
Immunotheraphy
Issue Date: 5-Jun-2025
Publisher: Informa UK Limited
Abstract: Perioperative 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.
Note: Reproducció del document publicat a: https://doi.org/10.1080/2162402X.2025.2513109
It is part of: OncoImmunology, 2025, vol. 14, num. 1
URI: https://hdl.handle.net/2445/222243
Related resource: https://doi.org/10.1080/2162402X.2025.2513109
ISSN: 2162-402X
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))



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