Departamento de Patología, Instituto Nacional de Cancerología, San Fernando 22, Colonia Sección XVI, Tlalpan, Ciudad de México 14050, Mexico.
Subdirección de Investigación Básica, Instituto Nacional de Cancerología, San Fernando 22, Colonia Sección XVI, Tlalpan, Ciudad de México 14050, Mexico.
Ann Diagn Pathol. 2023 Apr;63:152081. doi: 10.1016/j.anndiagpath.2022.152081. Epub 2023 Jan 17.
Recent studies have shown that the classification of high-grade urothelial carcinoma non-muscle invasive (HGBCNMI) based on molecular subtypes might be a valuable strategy to identify patients with a worse clinical prognosis.
Determine the effect of the luminal and basal molecular subtype determined by immunistochemical on prognosis in patients with HGBC in Mexican population.
Phenotypes were evaluated by immunohistochemical staining of luminal (GATA3, FOXA1) and basal (CK5/6, CK14) markers in paraffin-embedded tissue samples from 45 patients with a diagnosis of HGBCNMI treated at Instituto Nacional de Cancerología-México (INCan) between 2009 and 2019. The association with prognosis was evaluated using Kaplan-Meier curves and multivariable-adjusted Cox models.
HGBCNMI patients showed mean age of 58.77 years (SD: ±12.08 years). We identified expression of the luminal molecular subtype in 35 cases (77.78 %), and 10 cases (22.22 %) with "combined" expression of the molecular subtype (basal and luminal expression). The combined phenotype was statistically more frequent in metastatic cases (p-value = 0.028). In Kaplan-Meier curves, combined expression of luminal and basal molecular markers was associated with disease progression (p-value = 0.002, log-rank test). Cox regression models confirmed this association, which was not influenced by age (p-value = 0.007) or gender (p-value = 0.007). No association of phenotypes with overall survival (p-value = 0.860) or relapse (p-value = 0.5) was observed.
The combined expression of immunohistochemical markers of the luminal and basal subtype might be considered as predictor for disease progression in patients with HGBCNMI in Mexican population.
最近的研究表明,基于分子亚型对高级别尿路上皮癌非浸润性(HGBCNMI)进行分类可能是一种识别临床预后较差患者的有价值策略。
确定免疫组织化学检测的管腔和基底分子亚型在墨西哥人群中 HGBC 患者中的预后影响。
对 2009 年至 2019 年在墨西哥国家癌症研究所(INCan)接受治疗的 45 例 HGBCNMI 患者的石蜡包埋组织样本进行管腔(GATA3、FOXA1)和基底(CK5/6、CK14)标志物的免疫组织化学染色,评估表型。使用 Kaplan-Meier 曲线和多变量调整 Cox 模型评估与预后的关联。
HGBCNMI 患者的平均年龄为 58.77 岁(SD:±12.08 岁)。我们在 35 例(77.78%)中识别出管腔分子亚型的表达,在 10 例(22.22%)中识别出“组合”表达的分子亚型(基底和管腔表达)。在转移性病例中,联合表型更为常见(p 值=0.028)。在 Kaplan-Meier 曲线中,管腔和基底分子标记物的联合表达与疾病进展相关(p 值=0.002,对数秩检验)。Cox 回归模型证实了这种关联,且不受年龄(p 值=0.007)或性别(p 值=0.007)的影响。未观察到表型与总生存期(p 值=0.860)或复发(p 值=0.5)之间存在关联。
在墨西哥人群中,HGBCNMI 患者免疫组织化学标记物的管腔和基底亚型的联合表达可被视为疾病进展的预测因子。