Patel Jai N, Fong Mei Ka, Jagosky Megan
Department of Cancer Pharmacology, Levine Cancer Institute, Atrium Health, Charlotte, NC 28204, USA.
Department of Pharmacy, Levine Cancer Institute, Atrium Health, Charlotte, NC 28204, USA.
J Pers Med. 2019 Jan 14;9(1):3. doi: 10.3390/jpm9010003.
The 5-year survival probability for patients with metastatic colorectal cancer has not drastically changed over the last several years, nor has the backbone chemotherapy in first-line disease. Nevertheless, newer targeted therapies and immunotherapies have been approved primarily in the refractory setting, which appears to benefit a small proportion of patients. Until recently, rat sarcoma () mutations remained the only genomic biomarker to assist with therapy selection in metastatic colorectal cancer. Next generation sequencing has unveiled many more potentially powerful predictive genomic markers of therapy response. Importantly, there are also clinical and physiologic predictive or prognostic biomarkers, such as tumor sidedness. Variations in germline pharmacogenomic biomarkers have demonstrated usefulness in determining response or risk of toxicity, which can be critical in defining dose intensity. This review outlines such biomarkers and summarizes their clinical implications on the treatment of colorectal cancer. It is critical that clinicians understand which biomarkers are clinically validated for use in practice and how to act on such test results.
在过去几年中,转移性结直肠癌患者的5年生存概率没有显著变化,一线疾病的主要化疗方案也没有改变。然而,更新的靶向治疗和免疫治疗主要在难治性情况下获得批准,似乎仅使一小部分患者受益。直到最近,大鼠肉瘤()突变仍然是转移性结直肠癌中唯一有助于治疗选择的基因组生物标志物。新一代测序揭示了更多可能强大的治疗反应预测基因组标志物。重要的是,还有临床和生理预测或预后生物标志物,如肿瘤部位。种系药物基因组生物标志物的变异已证明在确定反应或毒性风险方面有用,这在确定剂量强度方面可能至关重要。本综述概述了此类生物标志物,并总结了它们对结直肠癌治疗的临床意义。临床医生了解哪些生物标志物在临床实践中得到验证以及如何根据此类检测结果采取行动至关重要。