Trojan Jörg, Klein-Scory Susanne, Koch Christine, Schmiegel Wolff, Baraniskin Alexander
Gastroenterology, Department of Medicine, Goethe University Frankfurt, Frankfurt, Germany.
IMBL Medical Clinic, Universitätsklinikum Knappschaftskrankenhaus Bochum, Bochum, Germany.
Case Rep Oncol Med. 2017;2017:6139634. doi: 10.1155/2017/6139634. Epub 2017 Jan 23.
Colorectal cancers (CRC) shed DNA into blood circulation. There is growing evidence that the analysis of circulating tumor DNA can be effectively used for monitoring of disease, to track tumor heterogeneity and to evaluate response to treatment. Here, we describe two cases of patients with advanced CRC. The first case is about a patient with no available tissue for analysis of RAS mutation status. Liquid biopsy revealed RAS-wild-type and the therapy with anti-EGFR (epidermal growth factor receptor) monoclonal antibody cetuximab could be initiated. In the second case, the mutational profile of a patient with initial wild-type RAS-status was continually tracked during the course of treatment. An acquired KRAS exon 3 mutation was detected. The number of KRAS mutated fragments decreased continuously after the discontinuation of the therapy with EGFR-specific antibodies. . Liquid biopsy provides a rapid genotype result, which accurately reproduces the current mutation status of tumor tissue. Furthermore, liquid biopsy enables close monitoring of the onset of secondary resistance to anti-EGFR therapy.
结直肠癌(CRC)会将DNA释放到血液循环中。越来越多的证据表明,循环肿瘤DNA分析可有效用于疾病监测、追踪肿瘤异质性以及评估治疗反应。在此,我们描述两例晚期CRC患者的病例。第一例是一名没有可用组织来分析RAS突变状态的患者。液体活检显示为RAS野生型,因此可以开始使用抗表皮生长因子受体(EGFR)单克隆抗体西妥昔单抗进行治疗。在第二例中,对一名初始RAS状态为野生型的患者在治疗过程中持续追踪其突变情况。检测到获得性KRAS外显子3突变。停用EGFR特异性抗体治疗后,KRAS突变片段数量持续下降。液体活检可快速得出基因型结果,准确再现肿瘤组织的当前突变状态。此外,液体活检能够密切监测抗EGFR治疗继发性耐药的发生。