所有亚型输卵管卵巢癌配对原发灶和转移灶中 claudin 18.2 的空间表达。

IF 3.4 3区 医学 Q1 PATHOLOGY
Virchows Archiv Pub Date : 2024-07-01 Epub Date: 2024-02-07 DOI:10.1007/s00428-024-03756-1
Paul Wagner, Paul Gass, Patrik Pöschke, Markus Eckstein, Laura Gloßner, Arndt Hartmann, Matthias Wilhelm Beckmann, Peter Andreas Fasching, Matthias Ruebner, Julius Emons, Ramona Erber
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引用次数: 0

摘要

从生理学角度看,CLDN18.2(Claudin 18 splice variant 2)的表达仅限于胃上皮细胞,但在实体瘤中也发现了它的表达。针对 CLDN18.2 的嵌合 IgG1 抗体唑贝妥昔单抗(Zolbetuximab)在 CLDN18.2 阳性、HER2 阴性的局部晚期胃癌患者中显示出良好的疗效,目前正在进一步研究中。迄今为止,人们对CLDN18.2在其他组织学亚型的输卵管卵巢癌(TOC)及其匹配转移灶中的表达知之甚少。我们利用一个包含所有组织学亚型TOC的队列,研究了CLDN18.2在TOC(536例)、匹配转移组织(385例)和93例无原发灶的转移灶中的免疫组化(IHC)表达。组织芯片包括肿瘤中心和外围。IHC阳性的定义是肿瘤细胞中生物标记物表达≥75%,并有中等至强膜状染色。CLDN18.2阳性率在TOC中心为4.1%(21/515),在其周边为3.6%(18/498)。在粘液性输卵管卵巢癌(MTOC)原发灶中,CLDN18.2阳性率分别为45%(18/40)和36.6%(15/41)。相应转移灶的阳性率分别为 33%(4/12,中心)和 27%(3/11,周边)。所有肿瘤部位的表达相对均匀。CLDN18.2在99.5%的非粘液性肿瘤中无表达,几乎只在粘液性亚型中出现阳性。在输卵管卵巢癌中,CLDN18.2的表达仅限于粘液性亚型,只有极少数例外。其中,33%的转移性 MTOC 呈 CLDN18.2 阳性。因此,CLDN18.2可能是晚期MTOC患者个体化治疗的一个有希望的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spatial expression of claudin 18.2 in matched primaries and metastases of tubo-ovarian carcinoma of all subtypes.

Spatial expression of claudin 18.2 in matched primaries and metastases of tubo-ovarian carcinoma of all subtypes.

Physiologically, claudin 18 splice variant 2 (CLDN18.2) expression is restricted to the gastric epithelium, but its expression has been detected in solid cancers. Zolbetuximab, a chimeric IgG1 antibody targeting CLDN18.2, has demonstrated promising effects in patients suffering from CLDN18.2-positive, HER2-negative locally advanced gastric cancer and is currently being studied further. To date, little is known about CLDN18.2 expression in other histological subtypes of tubo-ovarian carcinoma (TOC) and their matching metastases.Using a cohort of all histological TOC subtypes, we investigated the immunohistochemical (IHC) CLDN18.2 expression in both TOCs (n = 536), their matching metastatic tissue (n = 385) and in 93 metastases without primary. Tissue microarrays comprised both the tumor center and periphery. IHC positivity was defined as biomarker expression of ≥ 75% in tumor cells with moderate-to-strong membranous staining.Overall CLDN18.2 positivity was 4.1% (21/515) in the TOC centers and 3.6% (18/498) in their peripheries. In primaries of mucinous tubo-ovarian carcinoma (MTOC), CLDN18.2 positivity rates were 45% (18/40) and 36.6% (15/41), respectively. Positivity rates for the corresponding metastases were 33% (4/12, center) and 27% (3/11, periphery). The expression was relatively homogenous throughout all tumor sites. With no expression in 99.5% of nonmucinous tumors, CLDN18.2 positivity was almost exclusively seen in the mucinous subtype.In tubo-ovarian carcinoma, CLDN18.2 expression was, with rare exceptions, restricted to the mucinous subtype. Among them, 33% of metastasized MTOCs presented with CLDN18.2 positivity. Hence, CLDN18.2 might display a promising target for personalized therapy in patients with advanced MTOC.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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