[The impact of combined immunotherapy on the cellular composition of the tumor microenvironment in patients with gastric carcinoma].

Q4 Medicine
L A Tashireva, A Yu Kalinchuk, D M Loos, E A Tsarenkova, A V Avgustinovich, S G Afanas'ev, S V Vtorushin
{"title":"[The impact of combined immunotherapy on the cellular composition of the tumor microenvironment in patients with gastric carcinoma].","authors":"L A Tashireva, A Yu Kalinchuk, D M Loos, E A Tsarenkova, A V Avgustinovich, S G Afanas'ev, S V Vtorushin","doi":"10.17116/patol20258704124","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the impact of combined anti-PD-1 immunotherapy on the cellular composition of the tumor microenvironment in patients with gastric cancer.</p><p><strong>Material and methods: </strong>The study included 9 patients with morphologically confirmed gastric adenocarcinoma (stages T2-4N0-1M0) and positive PD-L1 status (CPS >1). All patients received 8 courses of preoperative chemotherapy according to the FLOT regimen, combined with additional immunotherapy using pembrolizumab (400 mg every 6 weeks). Changes in the tumor microenvironment were assessed using multicolor immunofluorescence followed by quantitative analysis of the proportions of CD8<sup>+</sup> cytotoxic T-lymphocytes, CD20<sup>+</sup> B-lymphocytes, CD163<sup>+</sup> macrophages, and FoxP3<sup>+</sup> regulatory T-cells.</p><p><strong>Results: </strong>A statistically significant increase in the number of CD8<sup>+</sup> T-lymphocytes (from 3.18% to 6.23%, <i>p</i>=0.0391) and, in particular, their PD-1-expressing subpopulation (from 0.00% to 0.22%, <i>p</i>=0.0156) was observed, while the numbers of CD20<sup>+</sup>, CD163<sup>+</sup>, and FoxP3<sup>+</sup> cells remained unchanged. As a result, the CD8<sup>+</sup>/FoxP3<sup>+</sup> cell ratio significantly increased during combined anti-PD-1 immunotherapy (from 0.69 to 3.22, <i>p</i>=0.0039). Additionally, associations were identified between immune parameters and clinicopathological characteristics, suggesting that gender and tumor stage may influence the immune response.</p><p><strong>Conclusion: </strong>The obtained data indicate a remodeling of the tumor microenvironment under the influence of anti-PD-1 therapy, which potentially enhances the antitumor immune response and opens prospects for further optimization of gastric cancer treatment.</p>","PeriodicalId":8548,"journal":{"name":"Arkhiv patologii","volume":"87 4","pages":"24-30"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arkhiv patologii","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17116/patol20258704124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To evaluate the impact of combined anti-PD-1 immunotherapy on the cellular composition of the tumor microenvironment in patients with gastric cancer.

Material and methods: The study included 9 patients with morphologically confirmed gastric adenocarcinoma (stages T2-4N0-1M0) and positive PD-L1 status (CPS >1). All patients received 8 courses of preoperative chemotherapy according to the FLOT regimen, combined with additional immunotherapy using pembrolizumab (400 mg every 6 weeks). Changes in the tumor microenvironment were assessed using multicolor immunofluorescence followed by quantitative analysis of the proportions of CD8+ cytotoxic T-lymphocytes, CD20+ B-lymphocytes, CD163+ macrophages, and FoxP3+ regulatory T-cells.

Results: A statistically significant increase in the number of CD8+ T-lymphocytes (from 3.18% to 6.23%, p=0.0391) and, in particular, their PD-1-expressing subpopulation (from 0.00% to 0.22%, p=0.0156) was observed, while the numbers of CD20+, CD163+, and FoxP3+ cells remained unchanged. As a result, the CD8+/FoxP3+ cell ratio significantly increased during combined anti-PD-1 immunotherapy (from 0.69 to 3.22, p=0.0039). Additionally, associations were identified between immune parameters and clinicopathological characteristics, suggesting that gender and tumor stage may influence the immune response.

Conclusion: The obtained data indicate a remodeling of the tumor microenvironment under the influence of anti-PD-1 therapy, which potentially enhances the antitumor immune response and opens prospects for further optimization of gastric cancer treatment.

[联合免疫治疗对胃癌患者肿瘤微环境细胞组成的影响]。
目的:探讨联合抗pd -1免疫治疗对胃癌患者肿瘤微环境细胞组成的影响。材料和方法:本研究纳入9例形态学证实的胃腺癌(T2-4N0-1M0期)和PD-L1阳性(CPS >1)的患者。所有患者均根据FLOT方案接受8个疗程的术前化疗,并联合使用派姆单抗进行额外的免疫治疗(每6周400mg)。采用多色免疫荧光法评估肿瘤微环境的变化,随后定量分析CD8+细胞毒性t淋巴细胞、CD20+ b淋巴细胞、CD163+巨噬细胞和FoxP3+调节性t细胞的比例。结果:CD8+ t淋巴细胞数量显著增加(从3.18%增加到6.23%,p=0.0391),特别是其表达pd -1的亚群(从0.00%增加到0.22%,p=0.0156),而CD20+、CD163+和FoxP3+细胞数量保持不变。结果,CD8+/FoxP3+细胞比值在联合抗pd -1免疫治疗期间显著增加(从0.69增加到3.22,p=0.0039)。此外,免疫参数与临床病理特征之间存在关联,表明性别和肿瘤分期可能影响免疫反应。结论:本研究结果提示抗pd -1治疗可改变肿瘤微环境,增强抗肿瘤免疫应答,为进一步优化胃癌治疗开辟了前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Arkhiv patologii
Arkhiv patologii Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
55
期刊介绍: The journal deals with original investigations on pressing problems of general pathology and pathologic anatomy, newest research methods, major issues of the theory and practice as well as problems of experimental, comparative and geographic pathology. To inform readers latest achievements of Russian and foreign medicine the journal regularly publishes editorial and survey articles, reviews of the most interesting Russian and foreign books on pathologic anatomy, new data on modern methods of investigation (histochemistry, electron microscopy, autoradiography, etc.), about problems of teaching, articles on the history of pathological anatomy development both in Russia and abroad.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信