Cytotoxic immune activity reflects a coordinated immune microenvironment and is associated with response to total neoadjuvant therapy in rectal cancer.

IF 5.7 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Erina Haraguchi, Norio Tanaka, Kentaro Sato, Tatsuki Noguchi, Takashi Sakamoto, Shimpei Matsui, Toshiki Mukai, Tomohiro Yamaguchi, Eiji Shinozaki, Senzo Taguchi, Akiko Chino, Manabu Takamatsu, Ippei Fukada, Takayuki Ueno, Tetsuo Noda, Seiichi Mori, Takashi Akiyoshi
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Abstract

Background: Total neoadjuvant therapy (TNT) has emerged as a promising treatment strategy for locally advanced rectal cancer; however, robust biomarkers predicting treatment response remain lacking. We aimed to identify pretreatment transcriptomic determinants of TNT response, focusing on cytotoxic immune activity and its broader immune context.

Methods: We analyzed two independent cohorts of patients with rectal cancer treated with TNT: a laser-capture microdissection (LCM) cohort (n = 154) and a bulk tumor cohort (n = 80). Differential gene expression, gene set enrichment, and immune deconvolution analyses were performed using pretreatment RNA sequencing data. Associations between cytotoxic activity and treatment response were evaluated using multivariable models.

Results: Only a limited number of genes were reproducibly associated with response across cohorts. Pathway-level analyses revealed enrichment of immune-related signatures in complete responders in the bulk cohort, whereas no significant enrichment was observed in the LCM cohort. Cytotoxic scores showed a consistent directional association with complete response in both cohorts, although modestly, and did not reach statistical significance in the LCM cohort. Cytotoxic activity was strongly correlated with multiple immune cell populations and signaling pathways, including effector and regulatory components, indicating a coordinated immune microenvironment. Multivariable analyses demonstrated that cytotoxic activity was independently associated with treatment response in the bulk cohort and recurrence-free survival in the LCM cohort.

Conclusions: Cytotoxic immune activity represents a biologically relevant but modest determinant of response to TNT in rectal cancer. These findings suggest that treatment sensitivity is shaped by a coordinated immune microenvironment rather than cytotoxic activity alone.

细胞毒性免疫活性反映了一个协调的免疫微环境,并与对直肠癌新辅助治疗的反应有关。
背景:全面新辅助治疗(TNT)已成为局部晚期直肠癌的一种有前景的治疗策略;然而,预测治疗反应的可靠生物标志物仍然缺乏。我们的目的是确定TNT反应的预处理转录组决定因素,重点关注细胞毒性免疫活性及其更广泛的免疫背景。方法:我们分析了两个独立的接受TNT治疗的直肠癌患者队列:激光捕获显微解剖(LCM)队列(n = 154)和大块肿瘤队列(n = 80)。使用预处理RNA测序数据进行差异基因表达、基因集富集和免疫反褶积分析。使用多变量模型评估细胞毒性活性与治疗反应之间的关系。结果:只有有限数量的基因可重复地与整个队列的反应相关。通路水平分析显示,在整体队列中完全应答者的免疫相关特征丰富,而在LCM队列中没有观察到显著的富集。在两个队列中,细胞毒性评分显示出与完全缓解一致的定向关联,尽管程度不大,但在LCM队列中没有达到统计学意义。细胞毒活性与多种免疫细胞群和信号通路密切相关,包括效应和调节成分,表明免疫微环境协调一致。多变量分析表明,细胞毒活性与大剂量队列的治疗反应和LCM队列的无复发生存独立相关。结论:细胞毒性免疫活性是直肠癌对TNT反应的生物学相关但适度的决定因素。这些发现表明,治疗敏感性是由协调的免疫微环境而不是单独的细胞毒性活性形成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Gastroenterology
Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
12.20
自引率
1.60%
发文量
99
审稿时长
4-8 weeks
期刊介绍: The Journal of Gastroenterology, which is the official publication of the Japanese Society of Gastroenterology, publishes Original Articles (Alimentary Tract/Liver, Pancreas, and Biliary Tract), Review Articles, Letters to the Editors and other articles on all aspects of the field of gastroenterology. Significant contributions relating to basic research, theory, and practice are welcomed. These publications are designed to disseminate knowledge in this field to a worldwide audience, and accordingly, its editorial board has an international membership.
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