Luchini Claudio, Matkowskyj Kristina A, Kuwata Takeshi, Longacre Teri A, Schirmacher Peter, Takamatsu Manabu, Rüschoff Josef, Fassan Matteo
Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
ARC-Net Research Center, University of Verona, Piazzale Scuro, 10, 37134, Verona, Italy.
Virchows Arch. 2025 Aug 21. doi: 10.1007/s00428-025-04222-2.
The evaluation of claudin-18 (CLDN18) by immunohistochemistry (IHC) has already entered routine diagnostic activity as a predictive biomarker for patients with gastric and gastroesophageal junction adenocarcinomas. Of note, the CLDN18 gene encodes for 2 isoforms, claudin-18.1 (CLDN18.1) and 18.2 (CLD18.2). Recent evidence has shown CLDN18.2 can be expressed in a relatively high rate of cases of pancreatic ductal adenocarcinoma (PDAC). Based on these findings, preclinical research has been conducted, and clinical trials are currently underway testing anti-CLDN18.2 targeted regimens for patients affected by locally advanced unresectable and metastatic PDAC. Notably, the therapeutic strategies with specific antibodies are directed against CLDN18.2, while the antibody for IHC recognizes both isoforms, CLDN18.1 and CLDN18.2. Since CLDN18.1 is not expressed in the stomach or in the pancreas, IHC for CLDN18 in these sites can be considered specific for the isoform CLD18.2. At this time, no specific practical testing or interpretation guidelines have been proposed in this setting. However, there are several preanalytical and analytical variables and key potential pancreas-specific pitfalls, such as the frequently diffuse and strong CLDN18.2 expression in PDAC precursors, which will likely interfere with adequate CLDN18 staining and interpretation. To overcome these issues and steer the standardization of CLDN18 evaluation within the PDAC framework, this manuscript provides practical guidance on CLDN18 testing and scoring. The adoption of a standardized approach will help align all the efforts, both in research and clinical trial settings to optimally guide the most appropriate patients for anti-CLDN18.2 targeted therapies in PDAC.
通过免疫组织化学(IHC)评估紧密连接蛋白18(CLDN18)已作为胃和胃食管交界腺癌患者的预测生物标志物进入常规诊断活动。值得注意的是,CLDN18基因编码两种异构体,紧密连接蛋白18.1(CLDN18.1)和18.2(CLD18.2)。最近的证据表明,CLDN18.2在相当比例的胰腺导管腺癌(PDAC)病例中可表达。基于这些发现,已经开展了临床前研究,目前正在进行临床试验,测试针对局部晚期不可切除和转移性PDAC患者的抗CLDN18.2靶向治疗方案。值得注意的是,特定抗体的治疗策略针对CLDN18.2,而用于IHC的抗体识别两种异构体,CLDN18.1和CLDN18.2。由于CLDN18.1在胃或胰腺中不表达,这些部位CLDN18的IHC可被认为对异构体CLD18.2具有特异性。目前,在这种情况下尚未提出具体的实际检测或解释指南。然而,存在几个分析前和分析变量以及关键的潜在胰腺特异性陷阱,例如PDAC前体中CLDN18.2经常弥漫性和强表达,这可能会干扰CLDN18的充分染色和解释。为了克服这些问题并推动PDAC框架内CLDN18评估的标准化,本手稿提供了关于CLDN18检测和评分的实用指南。采用标准化方法将有助于协调研究和临床试验环境中的所有努力,以最佳地指导PDAC中最适合接受抗CLDN18.2靶向治疗的患者。