Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.
Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, Georgia.
Ophthalmology. 2018 Feb;125(2):203-209. doi: 10.1016/j.ophtha.2017.07.018. Epub 2017 Aug 18.
To examine the BRCA1-associated protein-1 (BAP1) expression of primary uveal melanomas without and with metastasis, and to analyze the correlation between the BAP1 immunoreactivity of primary uveal melanoma and other clinicopathologic features.
Retrospective case series.
Forty patients with uveal melanoma (mean age, 57.98±14.75 years) were included in this analysis, of whom 20 had no metastatic disease and 20 had metastasis.
Medical records and histology slides of patients with primary uveal melanoma treated by enucleation were reviewed. BAP1 expression was evaluated by immunohistochemical staining of formalin-fixed, paraffin-embedded sections. Immunoreactivity in the nucleus and cytoplasm were graded by estimating the percentage of primary tumor cells showing a positive staining of their nucleus or cytoplasm per 1 high-power field 200× (grades 0-3).
Tumor size, histologic features, nuclear and cytoplasmic BAP1 immunoreactivity grade, and patient outcome, including development of metastasis.
Significantly lower (P = 0.025) nuclear BAP1 immunoreactivity was observed in the metastatic melanoma group. Greater tumor thickness, basal diameter, and more advanced TNM stage were associated with an increased odds ratio of developing metastasis (P < 0.05). In addition, tumors with a higher proportion of cells expressing nuclear BAP1 had decreased odds of developing metastatic disease in a multivariate model (P = 0.042). Metastasis-free survival was significantly longer in patients with uveal melanoma with high nuclear BAP1 stain (P = 0.004).
Time to metastasis differs in patients with primary uveal melanoma with different grades of nuclear BAP1 immunoreactivity. Nuclear BAP1 stain is the only significant independent predictor of metastatic disease in this study. Our data support the role of BAP1 immunohistochemical staining of primary uveal melanoma to evaluate metastatic risk.
研究无转移和有转移的原发性葡萄膜黑色素瘤中 BRCA1 相关蛋白-1(BAP1)的表达,并分析原发性葡萄膜黑色素瘤中 BAP1 免疫反应与其他临床病理特征之间的相关性。
回顾性病例系列研究。
本分析纳入了 40 名接受眼窝切除术治疗的葡萄膜黑色素瘤患者(平均年龄 57.98±14.75 岁),其中 20 名患者无转移疾病,20 名患者有转移。
回顾性分析了原发性葡萄膜黑色素瘤患者的病历和组织学切片。通过对福尔马林固定、石蜡包埋切片进行免疫组织化学染色,评估 BAP1 的表达。通过估计每 1 高倍视野(200×)中显示核或细胞质阳性染色的原发性肿瘤细胞的百分比(0-3 级),对核和细胞质内的免疫反应性进行分级。
肿瘤大小、组织学特征、核和细胞质 BAP1 免疫反应性分级以及包括转移在内的患者结局。
转移性黑色素瘤组的核 BAP1 免疫反应性显著降低(P=0.025)。肿瘤厚度、基底直径较大和更晚期的 TNM 分期与发生转移的几率增加相关(P<0.05)。此外,在多变量模型中,具有更高比例表达核 BAP1 的肿瘤发生转移的几率降低(P=0.042)。核 BAP1 染色高的葡萄膜黑色素瘤患者无转移生存时间显著延长(P=0.004)。
不同核 BAP1 免疫反应性的原发性葡萄膜黑色素瘤患者的转移时间不同。核 BAP1 染色是本研究中唯一有意义的独立预测转移性疾病的因素。我们的数据支持对原发性葡萄膜黑色素瘤进行 BAP1 免疫组化染色以评估转移风险的作用。