Sharett Institute of Oncology, Hadassah Medical Organization, Jerusalem, Israel.
Cancer Biomark. 2010;6(3-4):191-6. doi: 10.3233/CBM-2009-0129.
As the release and amount of circulating biomarkers show considerable variations between individuals, single value determinations are often difficult to be interpreted on their diagnostic or prognostic significance on the individual level. However, changes of the biomarker levels in a specific person during the disease course are quite informative for the estimation of the efficacy of therapy or the early detection of recurrent disease because they consider only intraindividual variations. If methods for marker determination are maintained, preanalytical and analytical standard prerequistits are respected, thresholds for each marker have to be defined which exceeds the normal, intraindividual biological variation. Then continuous biomarker increases may be indicative for disease activity in terms of inefficient therapy response or tumor recurrence while decreasing values often are associated with activity reduction of cancer disease. Here, we review the current knowledge on biomarker kinetics in patients with non-small cell lung cancer (NSCLC) and discuss the conditions and pitfalls of their relevance for the estimation efficacy of therapy and the early detection of recurrent disease. Further, we suggest a scenario to reveal the power of the defined biomarker use in future and to include those markers into the individual management of NSCLC patients.
由于循环生物标志物的释放和数量在个体之间表现出相当大的差异,因此单个值的测定通常难以解释其在个体水平上的诊断或预后意义。然而,在疾病过程中特定个体中生物标志物水平的变化对于评估治疗效果或早期发现复发性疾病非常有信息意义,因为它们只考虑个体内的变化。如果用于标志物测定的方法得到维持,并且符合预分析和分析标准,则必须为每个标志物定义一个阈值,该阈值超过正常的个体内生物学变异。然后,连续的生物标志物增加可能表明治疗反应无效或肿瘤复发的疾病活动,而降低的值通常与癌症疾病活动减少相关。在这里,我们回顾了非小细胞肺癌 (NSCLC) 患者中生物标志物动力学的现有知识,并讨论了它们对评估治疗效果和早期发现复发性疾病的相关性的条件和陷阱。此外,我们提出了一种方案,以揭示定义的生物标志物使用在未来的力量,并将这些标志物纳入 NSCLC 患者的个体化管理中。