Institute for Pathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Ann Oncol. 2012 Sep;23 Suppl 10:x63-70. doi: 10.1093/annonc/mds346.
In recent years, colorectal cancer (CRC), once a uniform disease with well-understood carcinogenesis, has been divided into at least five different subgroups with distinct precursor lesions, pathways of carcinogenesis, morphological, and molecular characteristics. Moreover, new therapeutic concepts with 'targeted' substances have added to the complexity of the management of CRC patients. The clinical value of biomarkers in advanced CRC is indisputable ever since activating mutations of the KRAS oncogene have been shown to predict resistance to anti-epidermal growth factor receptor antibodies. Prognostic biomarkers predicting patient outcomes and predictive biomarkers forecasting response to a certain therapy may help us to improve therapeutic agent selection and patient management with the ultimate goal of maximizing the benefit of treatment and minimizing toxicity. Biomarkers with known implications in advanced CRC will be discussed in this paper.
近年来,结直肠癌(CRC)曾经是一种具有明确致癌机制的单一疾病,现已至少分为五个不同的亚组,具有不同的前期病变、致癌途径、形态学和分子特征。此外,具有“靶向”物质的新治疗概念增加了 CRC 患者管理的复杂性。自从激活的 KRAS 癌基因突变被证明可预测抗表皮生长因子受体抗体的耐药性以来,生物标志物在晚期 CRC 中的临床价值已不容置疑。预测患者结局的预后生物标志物和预测对某种治疗反应的预测生物标志物可能有助于我们改善治疗药物的选择和患者管理,最终目的是最大限度地提高治疗益处并降低毒性。本文将讨论在晚期 CRC 中具有明确影响的生物标志物。