循环肿瘤DNA
内科学
肿瘤科
液体活检
转移性乳腺癌
循环肿瘤细胞
乳腺癌
癌症
生物标志物
转移
克拉斯
作者
Qing Wei,Yinjie Zhang,Jing Gao,Jian Li,Jie Li,Yanyan Li,Jun Zhou,Ming Lu,Jifang Gong,Xiaotian Zhang,Lin Shen,Yu Sun,Lianpeng Chang,Xicheng Wang
标识
DOI:10.1016/j.clcc.2019.05.001
摘要
Abstract Background Therapy targeting human epidermal growth factor receptor 2 (HER2, also known as ERBB2) is an effective approach for HER2-positive metastatic colorectal cancer (mCRC). HER2 status is typically determined using immunohistochemistry and fluorescence in situ hybridization. Circulating tumor DNA (ctDNA) enables noninvasive detection of gene mutations and copy number alterations including HER2 amplification. Materials and Methods We screened 351 patients with mCRC and studied the clinicopathologic characteristics of HER2-positive mCRC. HER2 expression in tumor samples measured with immunohistochemistry and fluorescence in situ hybridization was compared with HER2 copy number variation in plasma ctDNA detected by targeted sequence capture covering exons of 170 genes. We also examined the correlation between changes in tumor burden in ctDNA and antitumor response by imaging evaluation during the treatment course. Results Positive HER2 status was observed in 12 (3.4%) patients (7 males and 5 females), with a median age of 56 years. The HER2 concordance rate between tumor samples and ctDNA was 66.7% (20/30). Changes in tumor burden in ctDNA during the treatment course correlated with responses on imaging. Conclusions Detection of HER2 copy number variation in ctDNA may be an alternative option for noninvasive determination of HER2 status. Tumor burden changes in ctDNA were consistent with imaging evaluation.
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