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
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.
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