Duffy Michael J, McDermott Enda W, Crown John
1 Clinical Research Centre, St. Vincent's University Hospital, Dublin, Ireland.
2 UCD School of Medicine, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
Tumour Biol. 2018 May;40(5):1010428318776169. doi: 10.1177/1010428318776169.
Biomarkers are the key to personalized treatment in patients with breast cancer. While tissue biomarkers are most useful in determining prognosis and upfront predicting response to therapy, circulating protein biomarkers such as CA 15-3 and carcinoembryonic antigen are mainly used in monitoring response to endocrine or chemotherapy in patients with advanced disease. Although several centers measure biomarkers in asymptomatic patients following curative surgery for primary breast cancer, the clinical utility of this practice is unclear. Promising new biomarkers for breast cancer include circulating tumor DNA and circulating tumor cells. In contrast to circulating protein biomarkers, measurement of circulating tumor DNA-based biomarkers is potentially useful in identifying mechanisms of resistance to ongoing therapies as well as identifying new targets for further treatment. To increase clinical utility, both the established and emerging circulating biomarkers should where possible be incorporated into randomized trials evaluating new therapies in patients with breast cancer.
生物标志物是乳腺癌患者个性化治疗的关键。组织生物标志物在确定预后和预先预测治疗反应方面最有用,而循环蛋白生物标志物如CA 15-3和癌胚抗原主要用于监测晚期疾病患者对内分泌或化疗的反应。尽管几个中心在原发性乳腺癌根治性手术后对无症状患者进行生物标志物检测,但这种做法的临床实用性尚不清楚。有前景的乳腺癌新生物标志物包括循环肿瘤DNA和循环肿瘤细胞。与循环蛋白生物标志物不同,基于循环肿瘤DNA的生物标志物检测在识别对现有疗法的耐药机制以及确定进一步治疗的新靶点方面可能有用。为了提高临床实用性,应尽可能将已确立和新出现的循环生物标志物纳入评估乳腺癌患者新疗法的随机试验中。