Department of Pathology, University of Southern California/Norris Comprehensive Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Cancer J. 2010 May-Jun;16(3):262-72. doi: 10.1097/PPO.0b013e3181e07738.
Although significant progress has been made in colorectal cancer (CRC) treatment within the last decade with the approval of multiple new agents, the prognosis for patients with metastatic CRC remains poor with 5-year survival rates of approximately 8%. Resistance to chemotherapy remains a major obstacle in effective CRC treatment and many patients do not receive any clinical benefit from chemotherapy. In addition, other patients will experience adverse reactions to treatment resulting in dose modifications or treatment withdrawal, which can severely reduce treatment efficacy. Currently, significant research efforts are attempting to identify reliable and validated biomarkers with which will guide clinicians to make more informed treatment decisions. Specifically, the use of molecular profiling has the potential to assist the clinician in administering the correct drug, dose, or intervention for the patient before the onset of therapy thereby selecting a treatment strategy likely to have the greatest clinical outcome while minimizing adverse events. However, until recently, personalized medicine is a paradigm that has existed more in conceptual terms than in reality with very few validated biomarkers used routinely in metastatic CRC treatment. Rapid advances in genomic, transcriptomic and proteomic technologies continues to improve our understanding of tumor biology, but the search for reliable biomarkers has turned out to be more challenging than previously anticipated with significant disparity in published literature and limited translation into routine clinical practice. Recent progress with the identification and validation of biomarkers to the anti-epidermal growth factor receptor monoclonal antibodies including KRAS and possibly BRAF provide optimism that the goal of individualized treatment is within reach. This review will highlight and discuss current progress in the search for biomarkers, the challenges this emerging field presents, and the future role of biomarkers in advancing CRC treatment.
尽管在过去十年中,随着多个新药物的批准,在结直肠癌(CRC)治疗方面取得了重大进展,但转移性 CRC 患者的预后仍然很差,5 年生存率约为 8%。对化疗的耐药性仍然是 CRC 有效治疗的主要障碍,许多患者没有从化疗中获得任何临床益处。此外,其他患者会对治疗产生不良反应,导致剂量调整或治疗中止,这会严重降低治疗效果。目前,大量研究工作正在试图确定可靠和经过验证的生物标志物,以指导临床医生做出更明智的治疗决策。具体来说,分子谱分析有可能帮助临床医生在治疗开始前为患者选择正确的药物、剂量或干预措施,从而选择最有可能产生最大临床效果同时最小化不良反应的治疗策略。然而,直到最近,个性化医疗才更多地存在于概念层面,而不是现实中,很少有经过验证的生物标志物被常规用于转移性 CRC 的治疗。基因组学、转录组学和蛋白质组学技术的快速发展继续加深我们对肿瘤生物学的理解,但寻找可靠的生物标志物比预期的更具挑战性,发表的文献存在显著差异,并且在转化为常规临床实践方面受到限制。最近在鉴定和验证针对抗表皮生长因子受体单克隆抗体的生物标志物方面取得的进展,包括 KRAS 和可能的 BRAF,这让人乐观地认为个体化治疗的目标即将实现。这篇综述将重点介绍和讨论寻找生物标志物的最新进展、这一新兴领域所面临的挑战,以及生物标志物在推进 CRC 治疗方面的未来作用。