Department of Pathology, The University of Alabama at Birmingham, WP Building, Suite P230, 619 19th Street South, Birmingham, AL, 35249-7331, USA.
Department of Scientific Research, School of Postgraduate Studies, Norte University, Asuncion, Paraguay.
Virchows Arch. 2019 Sep;475(3):349-356. doi: 10.1007/s00428-019-02618-5. Epub 2019 Jul 12.
The Cancer Genome Atlas project introduced genomic taxonomy of basal and luminal molecular subtypes in muscle invasive bladder cancer. Fewer studies have addressed the molecular classification in non-muscle invasive bladder cancer (NMIBC). Our aim is to assess the applicability of the proposed phenotypic classification for NMIBC. Three TMAs were constructed from 193 TURBT specimens of 60 bladder cancer patients treated at one of the authors' institutions (1998-2008). Follow-up data on recurrence, grade, or stage progression was obtained. Immunohistochemistry was performed using an automated Ventana System for markers indicative of luminal (GATA3, CK20, ER, Uroplakin II, and HER2/neu) and basal (CK5/6 and CD44) phenotype. Marker expression was evaluated by 3 urologic pathologists. Using unadjusted logistic regression, we found significant association between tumor recurrence at next biopsy and CD44 expression (OR = 2.51, P = 0.03), tumor recurrence at any subsequent biopsy and ER expression (OR = 0.24, P = 0.04), and tumor grade progression at any subsequent biopsy and HER2/neu expression (OR = 0.24, P = 0.04). After adjusting for pathologic stage, we found a significant association between CK5/6 expression and tumor stage progression at either next or any subsequent biopsy (OR = 0.94, P = 0.006; and OR = 0.97, P = 0.02, respectively). Our findings suggest that individual immunohistochemical markers may be of value as prognostic factors in NMIBC.
癌症基因组图谱项目介绍了肌层浸润性膀胱癌中基底和腔面分子亚型的基因组分类。较少的研究涉及非肌层浸润性膀胱癌(NMIBC)的分子分类。我们的目的是评估所提出的表型分类在 NMIBC 中的适用性。从作者所在机构的 60 例膀胱癌患者的 193 例 TURBT 标本中构建了 3 个 TMA。获得了关于复发、分级或分期进展的随访数据。使用自动 Ventana 系统对标记物进行免疫组织化学染色,这些标记物提示腔面(GATA3、CK20、ER、Uroplakin II 和 HER2/neu)和基底(CK5/6 和 CD44)表型。由 3 位泌尿科病理学家评估标志物表达。使用未经调整的逻辑回归,我们发现下一次活检时肿瘤复发与 CD44 表达之间存在显著关联(OR=2.51,P=0.03),任何随后的活检时肿瘤复发与 ER 表达之间存在显著关联(OR=0.24,P=0.04),任何随后的活检时肿瘤分级进展与 HER2/neu 表达之间存在显著关联(OR=0.24,P=0.04)。在调整病理分期后,我们发现 CK5/6 表达与下一次或任何随后的活检时肿瘤分期进展之间存在显著关联(OR=0.94,P=0.006;OR=0.97,P=0.02)。我们的研究结果表明,个别免疫组织化学标志物可能作为 NMIBC 的预后因素具有一定价值。