Immunohistochemical profile of molecularly verified clear cell renal cell carcinomas.

IF 3.8 2区 医学 Q2 CELL BIOLOGY
Histopathology Pub Date : 2026-10-01 DOI:10.1111/his.70287
Kara S Tanaka, Li Zhang, Chien-Kuang Cornelia Ding, Nancy Y Greenland, Jeffry P Simko, Bradley A Stohr, Deepika Sirohi
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引用次数: 0

Abstract

Background: Immunohistochemical (IHC) features of clear cell renal cell carcinomas (CCRCC) have historically been defined by morphologically selected tumours, but aberrant staining patterns that may confound the diagnosis are common. Recent studies have described the prognostic significance of architectural patterns in CCRCC and have proposed grading schemes based on morphology. We investigate a cohort of molecularly verified CCRCC to evaluate their IHC profiles and correlate with architectural patterns and key driver molecular alterations.

Methods: Renal cell carcinomas (RCCs) sequenced at our institution between January 2015 and June 2024 by NGS assay were reviewed to identify CCRCCs based on VHL alterations and/or 3p loss. Architectural patterns were classified into low grade (LG) (nested, cystic), intermediate grade (IG) (tubular, tubulopapillary, alveolar), and high grade (HG) (fused nests/solid sheets, rhabdoid, sarcomatoid, low-grade spindled, pleomorphic tumour giant cells), based on findings from recent studies and scored based on highest-grade pattern. IHC staining for CA9, KER7, PAX8, and CD10 were reviewed for percent staining (focal 25% or less, moderate 26%-50%, diffuse greater than 50%). Correlation of aberrant staining with primary/metastatic status, architectural patterns, and molecular alterations was analysed.

Results: 125 cases of molecularly verified CCRCC were identified and 108 cases with concurrent IHC met inclusion criteria, including 54 primary and 54 metastatic tumours. KER7 positivity was more common in primary vs. metastatic tumours (45% vs. 13%, P = 0.001), in tumours with LG/IG architectural patterns (67% LG and 67% IG vs. 17% HG, P = 0.002) and in PBRM1 wild type (WT) tumours (84% PBRM1 WT vs. 16% PBRM1 mutated, P = 0.021). Negative CA9 staining occurred only in metastatic tumours (15%). PBRM1 mutated tumours were more likely to be KER7-/CA9+/PAX8-, while BAP1 mutated tumours were more likely to have higher-grade architectural patterns and lack CD10 expression.

Conclusions: In this cohort of molecularly verified CCRCCS, positive KER7 staining was seen in 30% of tumours with diffuse strong staining in 16%. The IHC profiles correlated with both morphological features and genetic alterations.

分子证实的透明细胞肾细胞癌的免疫组织化学特征。
背景:透明细胞肾细胞癌(CCRCC)的免疫组织化学(IHC)特征历来是由形态学选择的肿瘤定义的,但异常的染色模式可能混淆诊断是常见的。最近的研究描述了CCRCC中建筑模式的预后意义,并提出了基于形态学的分级方案。我们研究了一组经过分子验证的CCRCC,以评估它们的IHC谱,并将其与建筑模式和关键驱动分子改变联系起来。方法:回顾2015年1月至2024年6月在我院通过NGS法测序的肾细胞癌(rcc),以确定基于VHL改变和/或3p缺失的ccrcc。根据最近的研究结果,将建筑模式分为低级别(LG)(巢状、囊状)、中级(IG)(管状、管状乳头状、肺泡状)和高级别(HG)(融合巢/实片状、横纹肌样、肉瘤样、低级别纺锤状、多形性肿瘤巨细胞),并根据最高级别模式进行评分。回顾IHC染色CA9、KER7、PAX8和CD10的染色百分比(局灶性25%或以下,中度26%-50%,弥漫性大于50%)。分析了异常染色与原发/转移状态、结构模式和分子改变的相关性。结果:经分子验证的CCRCC 125例,合并免疫组化的108例符合纳入标准,其中原发肿瘤54例,转移肿瘤54例。KER7阳性在原发性肿瘤和转移性肿瘤(45%对13%,P = 0.001)、LG/IG结构模式的肿瘤(67% LG和67% IG对17% HG, P = 0.002)和PBRM1野生型(WT)肿瘤(84% PBRM1 WT对16% PBRM1突变,P = 0.021)中更为常见。CA9阴性染色仅发生在转移性肿瘤中(15%)。PBRM1突变的肿瘤更可能是KER7-/CA9+/PAX8-,而BAP1突变的肿瘤更可能具有更高级别的结构模式和缺乏CD10表达。结论:在分子验证的CCRCCS队列中,30%的肿瘤可见KER7阳性染色,16%的肿瘤可见弥漫性强染色。IHC谱与形态学特征和遗传改变相关。
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来源期刊
Histopathology
Histopathology 医学-病理学
CiteScore
10.20
自引率
4.70%
发文量
239
审稿时长
1 months
期刊介绍: Histopathology is an international journal intended to be of practical value to surgical and diagnostic histopathologists, and to investigators of human disease who employ histopathological methods. Our primary purpose is to publish advances in pathology, in particular those applicable to clinical practice and contributing to the better understanding of human disease.
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