Peripheral memory B cell population maintenance and long-term survival after perioperative chemoimmunotherapy in NSCLC (NADIM trial).

IF 6.5 2区 医学 Q1 IMMUNOLOGY
Oncoimmunology Pub Date : 2025-12-01 Epub Date: 2025-06-05 DOI:10.1080/2162402X.2025.2513109
Belén Sierra Rodero, Cristina Martínez-Toledo, Ernest Nadal, Marta Molina-Alejandre, Rosario García Campelo, Ángeles Gil-González, Bartomeu Massuti, Aránzazu García-Grande, Manuel Dómine, Amelia Insa, Javier de Castro Carpeño, Gerardo Huidobro Vence, Margarita Majem, Alex Martinez-Marti, Diego Megias, Daniel Lobato, Ana Collazo-Lorduy, Virginia Calvo, Mariano Provencio, Alberto Cruz-Bermúdez
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引用次数: 0

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 naïve 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.

NSCLC围手术期化疗免疫治疗后外周记忆B细胞群维持和长期生存(NADIM试验)。
围手术期化疗免疫治疗显著提高了非小细胞肺癌(NSCLC)的生存率。然而,目前的组织生物标志物仍然不足,强调需要更敏感和更容易获得的替代品来监测复发风险。肿瘤内b细胞在增强免疫治疗效果方面的作用越来越得到认可,但外周b细胞对免疫监测的贡献仍未被探索。在NADIM临床试验(NCT03081689)中,对41例IIIA期NSCLC患者接受围手术期纳武单抗加化疗的血液样本(诊断时、新辅助治疗后、辅助治疗6个月和12个月)进行外周血b细胞免疫表型分析。结果与5年生存结果相关,并通过无监督聚类验证。在新辅助治疗结束至辅助治疗后6个月期间,观察到总b细胞(CD19+CD20+CD24+CD38+CD27-CD10-)和naïve b细胞(CD19+CD20+CD24+CD38+ cd27 -/lowCD27+)的比例增加,记忆b细胞(CD19+CD20+CD24+CD38+ +CD10+)的比例减少。在辅助治疗6个月和12个月时,总b细胞中CD20表达水平升高,以及记忆b细胞或活化b细胞(CD19+CD20+CD25+)的百分比增加,与生存率增加有关。相反,在辅助治疗期间,新描述的CD19+CD20lowCD25lowCD27low b细胞循环群的较高水平与疾病进展有关。可切除的非小细胞肺癌患者围手术期纳武单抗加化疗可诱导外周血b细胞发生显著变化。辅助治疗期间循环记忆b细胞的持续存在可能在存活中起关键作用。
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来源期刊
Oncoimmunology
Oncoimmunology ONCOLOGYIMMUNOLOGY-IMMUNOLOGY
CiteScore
12.50
自引率
2.80%
发文量
276
审稿时长
24 weeks
期刊介绍: OncoImmunology is a dynamic, high-profile, open access journal that comprehensively covers tumor immunology and immunotherapy. As cancer immunotherapy advances, OncoImmunology is committed to publishing top-tier research encompassing all facets of basic and applied tumor immunology. The journal covers a wide range of topics, including: -Basic and translational studies in immunology of both solid and hematological malignancies -Inflammation, innate and acquired immune responses against cancer -Mechanisms of cancer immunoediting and immune evasion -Modern immunotherapies, including immunomodulators, immune checkpoint inhibitors, T-cell, NK-cell, and macrophage engagers, and CAR T cells -Immunological effects of conventional anticancer therapies.
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