Interobserver Agreement in Vascular Invasion Scoring and the Added Value of Immunohistochemistry for Vascular Markers to Predict Disease Relapse in Stage I Testicular Nonseminomas

J. Lobo, H. Stoop, A. Gillis, L. Looijenga, W. Oosterhuis
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引用次数: 16

Abstract

Supplemental Digital Content is available in the text. Vascular invasion has been identified as an informative risk factor for relapse in stage I testicular nonseminomas, used to tailor treatment. We investigated interobserver agreement in vascular invasion reporting and studied the potential additional value of immunohistochemistry for vascular markers for predicting relapse. Patients (n=52) with stage I testicular nonseminomas undergoing surveillance (1993-2006) were included (median follow-up of 66 mo). Two formalin-fixed paraffin-embedded blocks with >1 cm2 tissue and tumor/normal parenchyma interface were stained with hematoxylin and eosin and CD31, FVIII, and D2-40. Slides were assessed by 3 independent testicular germ cell tumor-dedicated pathologists, and agreement was assessed using Cohen κ statistic. Sensitivity, specificity, and accuracy of vascular invasion scoring in predicting relapse were calculated. Agreement among testicular germ cell tumor-dedicated pathologists was moderate (κ=0.49 to 0.54), as was performance in predicting disease relapse (particularly, specificity of 86%). Immunohistochemistry increased overall sensitivity (71%), but decreased specificity (71%) in predicting relapse. All patients (n=8) with both blood and lymphatic vascular invasion developed a relapse. In multivariable analysis (including age, tumor size, rete testis invasion, and serum tumor markers), only vascular invasion had an independent impact in predicting relapse. Assessment of vascular invasion by testicular germ cell tumor-dedicated pathologists is good and is clinically meaningful, predicting disease relapse. Immunohistochemistry for vascular markers improves sensitivity of detecting disease relapse and allows for the identification of high-risk patients with both blood and lymphatic vascular invasion simultaneously, potentially of interest for tailored chemotherapy.
补充数字内容可在文本中找到。血管侵犯已被确定为I期睾丸非精原细胞瘤复发的重要危险因素,用于定制治疗。我们调查了在血管侵袭报告中观察者之间的一致性,并研究了免疫组织化学对血管标志物预测复发的潜在附加价值。接受监测的I期睾丸非精原细胞瘤患者(n=52)(中位随访66个月)被纳入研究。用苏木精、伊红和CD31、FVIII和D2-40染色两个>1 cm2组织和肿瘤/正常实质界面的福尔马林固定石蜡包埋块。由3名独立的睾丸生殖细胞肿瘤专业病理学家对载玻片进行评估,并采用Cohen κ统计量进行一致性评估。计算血管侵犯评分预测复发的敏感性、特异性和准确性。睾丸生殖细胞肿瘤病理学家之间的一致性中等(κ=0.49至0.54),在预测疾病复发方面的表现也是如此(特别是,特异性为86%)。免疫组化提高了预测复发的总体敏感性(71%),但降低了特异性(71%)。所有同时有血液和淋巴血管侵犯的患者(n=8)均复发。在多变量分析中(包括年龄、肿瘤大小、睾丸网浸润和血清肿瘤标志物),只有血管浸润对预测复发有独立影响。睾丸生殖细胞肿瘤专业病理学家对血管侵犯的评估良好,对预测疾病复发具有临床意义。血管标志物的免疫组织化学提高了检测疾病复发的敏感性,并允许同时识别血液和淋巴血管侵犯的高危患者,这可能对量身定制的化疗感兴趣。
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