Dynamic changes of claudin 18.2 expression after systemic therapy in gastric and esophagogastric junction cancer

IF 5.6 2区 医学 Q1 ONCOLOGY
Cancer Pub Date : 2026-10-07 DOI:10.1002/cncr.70632
Danni Zhu MD, Zhuoran Fang MD, Guangjun Jin MD, Jiang Chen MD, Yiming Lu MD, Teng Yang MSc, Ke Shen MD, Yunfu Shi PhD, Yuansheng Zheng MD, Weiwei Xu BPharm, Xiangdong Cheng PhD, Qing Wei PhD
{"title":"Dynamic changes of claudin 18.2 expression after systemic therapy in gastric and esophagogastric junction cancer","authors":"Danni Zhu MD,&nbsp;Zhuoran Fang MD,&nbsp;Guangjun Jin MD,&nbsp;Jiang Chen MD,&nbsp;Yiming Lu MD,&nbsp;Teng Yang MSc,&nbsp;Ke Shen MD,&nbsp;Yunfu Shi PhD,&nbsp;Yuansheng Zheng MD,&nbsp;Weiwei Xu BPharm,&nbsp;Xiangdong Cheng PhD,&nbsp;Qing Wei PhD","doi":"10.1002/cncr.70632","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Claudin 18.2 (CLDN18.2) is a promising therapeutic target in gastric/esophagogastric junction adenocarcinoma (GC/EGJC), but its dynamic expression during systemic therapy is unclear.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>CLDN18.2 expression by immunohistochemistry in paired tumor samples from 155 patients with advanced GC/EGJC was retrospectively evaluated before and after systemic therapy. CLDN18.2-positive was defined as ≥75% of viable tumor cells exhibiting moderate-to-strong (2+ or 3+) membranous staining.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Among all patients, 54 (34.84%) were CLDN18.2-positive. Following treatment, the proportion of CLDN18.2-positive patients increased significantly to 61 (39.35%) (<i>p</i> &lt; .001). Among patients who were CLDN18.2-negative at baseline, 57 (56.44%) showed increased expression after treatment, including 22 (21.78%) who converted to positive status. In contrast, among those CLDN18.2-positive at baseline, expression decreased in 35 patients (64.81%), with 15 (27.78%) converting to negative status (<i>p</i> &lt; .001). Among patients receiving chemotherapy alone (<i>n</i> = 25), 1 (4.00%) converted to negative and 5 (20.00%) converted to positive, whereas among those receiving chemotherapy combined with immunotherapy (<i>n</i> = 130), 14 (10.77%) converted to negative and 17 (13.08%) converted to positive (<i>p</i> = .45). A total of 131 patients (84.52%) demonstrated changes in CLDN18.2 expression following therapy, encompassing both conversions across the positivity threshold and fluctuations within the same classification.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>CLDN18.2 expression in GC/EGJC is dynamic and frequently altered after systemic therapy. These findings support reassessment of CLDN18.2 status before initiating CLDN18.2-targeted therapies.</p>\n </section>\n </div>","PeriodicalId":138,"journal":{"name":"Cancer","volume":"132 20","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2026-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cncr.70632","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Claudin 18.2 (CLDN18.2) is a promising therapeutic target in gastric/esophagogastric junction adenocarcinoma (GC/EGJC), but its dynamic expression during systemic therapy is unclear.

Methods

CLDN18.2 expression by immunohistochemistry in paired tumor samples from 155 patients with advanced GC/EGJC was retrospectively evaluated before and after systemic therapy. CLDN18.2-positive was defined as ≥75% of viable tumor cells exhibiting moderate-to-strong (2+ or 3+) membranous staining.

Results

Among all patients, 54 (34.84%) were CLDN18.2-positive. Following treatment, the proportion of CLDN18.2-positive patients increased significantly to 61 (39.35%) (p < .001). Among patients who were CLDN18.2-negative at baseline, 57 (56.44%) showed increased expression after treatment, including 22 (21.78%) who converted to positive status. In contrast, among those CLDN18.2-positive at baseline, expression decreased in 35 patients (64.81%), with 15 (27.78%) converting to negative status (p < .001). Among patients receiving chemotherapy alone (n = 25), 1 (4.00%) converted to negative and 5 (20.00%) converted to positive, whereas among those receiving chemotherapy combined with immunotherapy (n = 130), 14 (10.77%) converted to negative and 17 (13.08%) converted to positive (p = .45). A total of 131 patients (84.52%) demonstrated changes in CLDN18.2 expression following therapy, encompassing both conversions across the positivity threshold and fluctuations within the same classification.

Conclusion

CLDN18.2 expression in GC/EGJC is dynamic and frequently altered after systemic therapy. These findings support reassessment of CLDN18.2 status before initiating CLDN18.2-targeted therapies.

胃癌和食管胃结癌全身治疗后claudin 18.2表达的动态变化
背景CLDN18.2 (CLDN18.2)是胃/食管胃交界腺癌(GC/EGJC)的一个有前景的治疗靶点,但其在全身治疗中的动态表达尚不清楚。方法采用免疫组化方法对155例晚期GC/EGJC配对肿瘤标本进行系统性治疗前后的CLDN18.2表达评价。cldn18.2阳性定义为≥75%的活细胞显示中至强(2+或3+)膜染色。结果54例(34.84%)患者cldn18.2阳性。治疗后,cldn18.2阳性患者比例显著增加至61例(39.35%)(p < .001)。基线时cldn18.2阴性的患者中,57例(56.44%)治疗后表达升高,其中22例(21.78%)转为阳性。相比之下,在基线时cldn18.2阳性的患者中,35例(64.81%)患者表达下降,15例(27.78%)患者转化为阴性状态(p < .001)。在单独化疗患者(n = 25)中,1例(4.00%)转为阴性,5例(20.00%)转为阳性,而在化疗联合免疫治疗患者(n = 130)中,14例(10.77%)转为阴性,17例(13.08%)转为阳性(p = 0.45)。共有131名患者(84.52%)在治疗后表现出CLDN18.2表达的变化,包括跨越阳性阈值的转换和同一分类内的波动。结论CLDN18.2在GC/EGJC中的表达是动态的,并且在全身治疗后经常发生改变。这些发现支持在开始CLDN18.2靶向治疗之前重新评估CLDN18.2状态。
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
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
×
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
小红书