Claudin 18.2 Targeting: A Pan-Cancer Perspective

医学 克洛丹 癌症 临床试验 单克隆抗体 生物标志物 化疗 临床意义 肿瘤科 癌症研究 卵巢癌 胃食管交界处 表达式(计算机科学) 内科学 免疫疗法 单克隆 透视图(图形) 紧密连接 免疫学 细胞 临床研究 恶性肿瘤 选择(遗传算法) 免疫组织化学 生物信息学 癌细胞 临床实习
作者
Mina Nikanjam,Judith Pérez‐Granado,Mark W. Gramling,Bruno Larvol,Razelle Kurzrock
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:: OF1-OF14
标识
DOI:10.1158/1078-0432.ccr-26-0708
摘要

Claudin 18.2 (CLDN18.2) is exclusively expressed on gastric mucosal cell tight junctions with minimal expression in other healthy adult tissues. Prior studies assessed expression by immunohistochemistry, mainly membrane staining. The FDA CLDN18.2 threshold for zolbetuximab approval is ≥75% moderate to strong staining. Higher level expression has been seen in a number of cancers including (but not limited to) gastric, gastroesophageal junction (GEJ), pancreatic, and ovarian cancers. CLDN18.2 expression can change with treatment and can exhibit heterogeneity between tumor sites. Zolbetuximab is a recently FDA-approved anti-CLDN18.2 monoclonal antibody for first-line therapy of gastric/GEJ cancers in combination with chemotherapy based on the improvement in outcomes demonstrated in the biomarker selected populations of the SPOTLIGHT and GLOW trials. Given limited single-agent responses rates to zolbetuximab, a number of other CLDN18.2-directed therapies, including antibody-drug conjugates, CAR-T cells, and bispecific antibodies, are under exploration in clinical trials. Despite expression of CLDN18.2 on the gastric mucosa, these therapies have overall been tolerable in clinical trials, albeit with the use of aggressive anti-emetic regimens. Herein, we summarize CLDN18.2 expression in cancer along with clinical trials of zolbetuximab and other CLDN18.2-directed therapies. Given the variability in CLDN18.2 expression within and between tumor types, biomarker-driven approaches will be critical for patient selection in clinical trials and therapeutic approaches.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
板栗发布了新的文献求助10
刚刚
刚刚
2秒前
keith发布了新的文献求助20
2秒前
酷炫的发带完成签到,获得积分10
2秒前
3秒前
科研通AI6.4应助wbh采纳,获得10
3秒前
3秒前
molihuakai应助西瓜采纳,获得10
4秒前
4秒前
4秒前
5秒前
李健应助晨是采纳,获得10
5秒前
科研通AI6.4应助czw采纳,获得20
5秒前
5秒前
我是老大应助科研通管家采纳,获得30
6秒前
6秒前
6秒前
6秒前
ViVi完成签到 ,获得积分10
6秒前
汉堡包应助科研通管家采纳,获得10
6秒前
小马甲应助科研通管家采纳,获得10
7秒前
7秒前
斯文败类应助科研通管家采纳,获得10
7秒前
英俊的铭应助科研通管家采纳,获得10
7秒前
7秒前
7秒前
7秒前
彭于晏应助科研通管家采纳,获得10
7秒前
8秒前
SciGPT应助科研通管家采纳,获得10
8秒前
板栗完成签到,获得积分10
8秒前
嵇焱完成签到,获得积分10
9秒前
叶言发布了新的文献求助10
10秒前
小蘑菇应助HYD采纳,获得10
10秒前
Chris695发布了新的文献求助10
10秒前
XueqiW完成签到,获得积分10
11秒前
11秒前
11秒前
111完成签到,获得积分10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The anomeric effect 1000
Principles of town planning: translating concepts to applications 1000
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Nature-Inspired Computing: Concepts, Methodologies, Tools, and Applications 600
Perfectionism in School 600
Organizational Behavior 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7730181
求助须知:如何正确求助?哪些是违规求助? 9282086
关于积分的说明 20147427
捐赠科研通 7307691
什么是DOI,文献DOI怎么找? 3303445
关于科研通互助平台的介绍 2456214
邀请新用户注册赠送积分活动 2311841