Reibel Jesper
Department of Oral Pathology & Medicine, School of Dentistry, University of Copenhagen, 20 Nørre Allé, DK-2200 Copenhagen N, Denmark.
Crit Rev Oral Biol Med. 2003;14(1):47-62. doi: 10.1177/154411130301400105.
The concept of a two-step process of cancer development in the oral mucosa, i.e., the initial presence of a precursor subsequently developing into cancer, is well-established. Oral leukoplakia is the best-known precursor lesion. The evidence that oral leukoplakias are pre-malignant is mainly derived from follow-up studies showing that between < 1 and 18% of oral pre-malignant lesions will develop into oral cancer; it has been shown that certain clinical sub-types of leukoplakia are at a higher risk for malignant transformation than others. The presence of epithelial dysplasia may be even more important in predicting malignant development than the clinical characteristics. Three major problems, however, are attached to the importance of epithelial dysplasia in predicting malignant development: (1) The diagnosis is essentially subjective, (2) it seems that not all lesions exhibiting dysplasia will eventually become malignant and some may even regress, and (3) carcinoma can develop from lesions in which epithelial dysplasia was not diagnosed in previous biopsies. There is, therefore, a substantial need to improve the histologic assessment of epithelial dysplasia or, since epithelial dysplasia does not seem to be invariably associated with or even a necessary prerequisite for malignant development, it may be necessary to develop other methods for predicting the malignant potential of pre-malignant lesions. As a consequence of these problems, numerous attempts have been made to relate biological characteristics to the malignant potential of leukoplakias. Molecular biological markers have been suggested to be of value in the diagnosis and prognostic evaluation of leukoplakias. Markers of epithelial differentiation and, more recently, genomic markers could potentially be good candidates for improving the prognostic evaluation of precursors of oral cancer. As yet, one or a panel of molecular markers has not been determined that allows for a prognostic prediction of oral pre-cancer which is any more reliable than dysplasia recording. However, these new markers could be considered complementary to conventional prognostic evaluation.
口腔黏膜癌发生的两步过程,即最初存在前驱病变随后发展为癌症的概念已得到充分确立。口腔白斑是最广为人知的前驱病变。口腔白斑为癌前病变的证据主要来自随访研究,这些研究表明,<1%至18%的口腔癌前病变会发展为口腔癌;已表明某些临床亚型的白斑比其他亚型发生恶性转化的风险更高。上皮发育异常的存在在预测恶性发展方面可能比临床特征更为重要。然而,上皮发育异常在预测恶性发展的重要性方面存在三个主要问题:(1)诊断本质上是主观的,(2)似乎并非所有表现出发育异常的病变最终都会恶变,有些甚至可能消退,(3)癌症可从先前活检未诊断出上皮发育异常的病变发展而来。因此,迫切需要改进上皮发育异常的组织学评估,或者由于上皮发育异常似乎并非总是与恶性发展相关甚至不是其必要前提,可能有必要开发其他方法来预测癌前病变的恶性潜能。由于这些问题,人们进行了大量尝试,将生物学特征与白斑的恶性潜能联系起来。分子生物学标志物已被认为在白斑的诊断和预后评估中有价值。上皮分化标志物以及最近的基因组标志物可能是改善口腔癌前驱病变预后评估的良好候选者。然而,尚未确定一个或一组分子标志物能够比发育异常记录更可靠地预测口腔癌前病变的预后。不过,这些新标志物可被视为对传统预后评估的补充。