Vereecken Pierre, Cornelis Frank, Van Baren Nicolas, Vandersleyen Valérie, Baurain Jean-François
Department of Dermatology, Centre Hospitalier Valida and Cliniques Universitaires Saint-Luc, B-1082 Brussels, Belgium.
Dermatol Res Pract. 2012;2012:260643. doi: 10.1155/2012/260643. Epub 2012 Jan 12.
Many serum biomarkers have been evaluated in melanoma but their clinical significance remains a matter of debate. In this paper, a review of the serum biomarkers for melanoma will be detailed and will be discussed from the point of view of their practical usefulness. The expression of biomarkers can be detected intracellularly or on the cell membrane of melanoma cells or noncancer cells in association with the melanoma. Some of these molecules can then be released extracellularly and be found in body fluids such as the serum. Actually, with the emergence of new targeted therapies for cancer and the increasing range of therapeutic options, the challenge for the clinician is to assess the unique risk/response ratio and the prognosis for each patient. New serum biomarkers of melanoma progression and metastatic disease are still awaited in order to provide efficient rationale for followup and treatment choices. LDH as well as S100B levels have been correlated with poor prognosis in AJCC stage III/IV melanoma patients. However, the poor sensitivity and specificity of those markers and many other molecules are serious limitations for their routine use in both early (AJCC stage I and II) and advanced stages of melanoma (AJCC stage III and IV). Microarray technology and proteomic research will surely provide new candidates in the near future allowing more accurate definition of the individual prognosis and prediction of the therapeutic outcome and select patients for early adjuvant strategies.
许多血清生物标志物已在黑色素瘤中进行了评估,但其临床意义仍存在争议。本文将详细回顾黑色素瘤的血清生物标志物,并从其实用性的角度进行讨论。生物标志物的表达可在黑色素瘤细胞或与黑色素瘤相关的非癌细胞的细胞内或细胞膜上检测到。其中一些分子随后可释放到细胞外,并在血清等体液中被发现。实际上,随着癌症新靶向治疗方法的出现以及治疗选择范围的扩大,临床医生面临的挑战是评估每个患者独特的风险/反应比和预后。仍在期待黑色素瘤进展和转移性疾病的新血清生物标志物,以便为随访和治疗选择提供有效的依据。乳酸脱氢酶(LDH)以及S100B水平与美国癌症联合委员会(AJCC)III/IV期黑色素瘤患者的不良预后相关。然而,这些标志物以及许多其他分子的低敏感性和特异性严重限制了它们在黑色素瘤早期(AJCC I期和II期)和晚期(AJCC III期和IV期)的常规应用。微阵列技术和蛋白质组学研究肯定会在不久的将来提供新的候选标志物,从而更准确地定义个体预后并预测治疗结果,并为早期辅助治疗策略选择患者。