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口腔潜在恶性疾病异型增生分级和 DNA 倍性对恶性转化的预测价值。

Predictive value of dysplasia grading and DNA ploidy in malignant transformation of oral potentially malignant disorders.

机构信息

Clinical and Diagnostic Sciences, King's College London, Guy's Hospital, London, United Kingdom.

出版信息

Cancer Prev Res (Phila). 2013 Aug;6(8):822-31. doi: 10.1158/1940-6207.CAPR-13-0001. Epub 2013 Jun 12.

DOI:10.1158/1940-6207.CAPR-13-0001
PMID:23761273
Abstract

Dysplasia grading is widely used to assess risk of transformation in oral potentially malignant disorders despite limited data on predictive value. DNA ploidy analysis has been proposed as an alternative. This study examines the prognostic value for both tests used in a routine diagnostic setting to inform clinical management. A retrospective study of conventional dysplasia grading was conducted on 1,401 patients. DNA ploidy analysis was conducted on a subset of 273 patients and results correlated with clinical information, pathologic diagnosis, and outcome over 5 to 15 years. Malignant transformation occurred in 32 of 273 patients (12%) and, of these, 20 (63%) of preexisting index lesions were aneuploid. Of 241 patients not developing carcinoma, only 39 (16%) of index lesions were aneuploid. Epithelial dysplasia correlated with DNA ploidy status (P < 0.001). The overall positive predictive value for malignant transformation by DNA aneuploidy was 38.5% (sensitivity 65.2% and specificity 75%) and by severe dysplasia grade 39.5% (sensitivity 30% and specificity 98%). DNA diploid and tetraploid status had negative predictive value of 90% to 96%. Combining DNA ploidy analysis with dysplasia grading gives a higher predictive value than either technique alone. Each of three traditional dysplasia grades predicts a significantly different risk of carcinoma development and time to transformation. DNA ploidy analysis had equivalent predictive value and also detected additional risk lesions in the absence of dysplasia.

摘要

尽管关于预测价值的资料有限,发育不良分级仍广泛用于评估口腔潜在恶性疾病的转化风险。有人提出 DNA 倍性分析是一种替代方法。本研究在常规诊断环境中检查了这两种测试的预后价值,以便为临床管理提供信息。对 1401 例患者进行了常规发育不良分级的回顾性研究。对 273 例患者中的一部分进行了 DNA 倍性分析,并将结果与临床资料、病理诊断以及 5 至 15 年的结果相关联。在 273 例患者中,有 32 例(12%)发生恶性转化,其中 20 例(63%)的原有指数病变为非整倍体。在未发生癌的 241 例患者中,仅有 39 例(16%)的指数病变为非整倍体。上皮发育不良与 DNA 倍性状态相关(P < 0.001)。DNA 非整倍体恶性转化的总体阳性预测值为 38.5%(敏感性为 65.2%,特异性为 75%),3 级严重发育不良的阳性预测值为 39.5%(敏感性为 30%,特异性为 98%)。DNA 二倍体和四倍体状态的阴性预测值为 90%至 96%。将 DNA 倍性分析与发育不良分级相结合的预测价值高于单独使用任何一种技术。三种传统发育不良分级中的每一种都预测了明显不同的癌发生风险和转化时间。DNA 倍性分析具有等效的预测价值,并且在没有发育不良的情况下还可以检测到额外的风险病变。

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