Lee Ju-Han, Jeong Hoiseon, Choi Jung-Woo, Oh Hwa Eun, Kim Young-Sik
Department of Pathology, Korea University Ansan Hospital, Ansan-Si, Gyeonggi-Do, Republic of Korea.
Medicine (Baltimore). 2018 Oct;97(42):e12862. doi: 10.1097/MD.0000000000012862.
Liquid biopsies using circulating tumor DNA (ctDNA) and cell-free DNA (cfDNA) have been developed for early cancer detection and patient monitoring. To investigate the clinical usefulness of ctDNA aberrations and cfDNA levels in patients with breast cancer (BC), we conducted a meta-analysis of 69 published studies on 5736 patients with BC.
The relevant publications were identified by searching PubMed and Embase databases. The effect sizes of outcome parameters were pooled using a random-effects model.
The ctDNA mutation rates of TP53, PIK3CA, and ESR1 were approximately 38%, 27%, and 32%, respectively. High levels of cfDNA were associated with BCs rather than with healthy controls. However, these detection rates were not satisfactory for BC screening. Although the precise mechanisms have been unknown, high cfDNA levels were significantly associated with axillary lymph node metastasis (odds ratio [OR] = 2.148, P = .030). The ctDNA mutations were significantly associated with cancer recurrence (OR = 3.793, P < .001), short disease-free survival (univariate hazard ratio [HR] = 5.180, P = .026; multivariate HR = 3.605, P = .001), and progression-free survival (HR = 1.311, P = .013) rates, and poor overall survival outcomes (HR = 2.425, P = .007).
This meta-analysis demonstrates that ctDNA mutation status predicts disease recurrence and unfavorable survival outcomes, while cfDNA levels can be predictive of axillary lymph node metastasis in patients with BC.
利用循环肿瘤DNA(ctDNA)和游离DNA(cfDNA)进行的液体活检已被用于早期癌症检测和患者监测。为了研究ctDNA异常和cfDNA水平在乳腺癌(BC)患者中的临床应用价值,我们对69项已发表的关于5736例BC患者的研究进行了荟萃分析。
通过检索PubMed和Embase数据库确定相关出版物。使用随机效应模型汇总结局参数的效应量。
TP53、PIK3CA和ESR1的ctDNA突变率分别约为38%、27%和32%。高水平的cfDNA与BC相关,而非与健康对照相关。然而,这些检测率对于BC筛查并不令人满意。尽管确切机制尚不清楚,但高cfDNA水平与腋窝淋巴结转移显著相关(优势比[OR]=2.148,P=0.030)。ctDNA突变与癌症复发(OR=3.793,P<0.001)、无病生存期短(单因素风险比[HR]=5.180,P=0.026;多因素HR=3.605,P=0.001)、无进展生存期(HR=1.311,P=0.013)率以及总生存期差(HR=2.425,P=0.007)显著相关。
这项荟萃分析表明,ctDNA突变状态可预测疾病复发和不良生存结局,而cfDNA水平可预测BC患者的腋窝淋巴结转移。