Medical Oncology Department, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.
Clin Colorectal Cancer. 2011 Dec;10(4):279-89. doi: 10.1016/j.clcc.2011.03.030. Epub 2011 May 12.
Colorectal cancer is a leading cause of cancer mortality despite recent expansion of treatment options in metastatic colorectal cancer (mCRC). Our knowledge about key signaling pathways in colorectal tumors has contributed to the identification of specific molecular markers of response to targeted agents. In this review we discuss well-established and potential predictive biomarkers of benefit with epidermal growth factor receptor (EGFR) inhibitors. Data derived from multiple phase III trials have indicated that KRAS mutations can be considered a highly specific negative biomarker of response to anti-EGFR monoclonal antibodies. Other molecular aberrations in pathways downstream of EGFR such as BRAF, NRAS, and PIK3CA mutations, and PTEN loss are also reviewed. Moreover biomarkers of efficacy to classic chemotherapeutic agents as well as recent advances regarding high-throughput technologies and circulating tumor cells are also considered. Personalized cancer medicine in the mCRC scenario seems to be near reality, but validation of many biomarkers in prospective clinical trials is urgently warranted.
尽管转移性结直肠癌 (mCRC) 的治疗选择最近有所扩大,但结直肠癌仍然是癌症死亡的主要原因。我们对结直肠肿瘤中关键信号通路的了解有助于确定针对靶向药物反应的特定分子标志物。在这篇综述中,我们讨论了表皮生长因子受体 (EGFR) 抑制剂的既定和潜在的预测性生物标志物。来自多项 III 期试验的数据表明,KRAS 突变可以被认为是对抗 EGFR 单克隆抗体反应的高度特异性阴性生物标志物。EGFR 下游途径中的其他分子异常,如 BRAF、NRAS 和 PIK3CA 突变以及 PTEN 缺失,也进行了综述。此外,还考虑了经典化疗药物的疗效标志物以及关于高通量技术和循环肿瘤细胞的最新进展。在 mCRC 情况下,个性化癌症医学似乎即将成为现实,但迫切需要在前瞻性临床试验中验证许多生物标志物。