Department of Laboratory Genetics, University Hospital Kralovske Vinohrady, Srobarova 50, 100 34, Prague, Czech Republic.
Department of Oncology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Breast Cancer Res Treat. 2017 Dec;166(3):695-700. doi: 10.1007/s10549-017-4452-9. Epub 2017 Aug 16.
This study analyzes peripheral blood samples from breast cancer (BC) patients. CTCs from peripheral blood were enriched by size-based separation and were then cultivated in vitro. The primary aim of this study was to demonstrate the antigen independent CTC separation method with high CTC recovery. Subsequently, CTCs enriched several times during the treatment were characterized molecularly.
Patients with different stages of BC (N = 167) were included into the study. All patients were candidates for surgery, surgical diagnostics, or were undergoing chemotherapy. In parallel, 20 patients were monitored regularly and in addition to CTC presence, also CTC character was examined by qPCR, with special focus on HER2 and ESR status.
CTC positivity in the cohort was 76%. There was no significant difference between the tested groups, but the highest CTC occurrence was identified in the group undergoing surgery and similarly in the group before the start of neoadjuvant treatment. On the other hand, the lowest CTC frequencies were observed in the menopausal patient group (56%), ESR+ patient group (60%), and DCIS group (44.4%). It is worth noting that after completion of neoadjuvant therapy (NACT) CTCs were present in 77.7% of cases. On the other hand, patients under hormonal treatment were CTC positive only in 52% of cases.
Interestingly, HER2 and ESR status of CTCs differs from the status of primary tumor. In 50% of patients HER2 status on CTCs changed not only from HER2+ to HER2-, but also from HER2- to HER2+ (33%). ESR status in CTCs changed only in one direction from ESR+ to ESR-.
Data obtained from the present study suggest that BC is a heterogeneous disease but CTCs may be detected independently of the disease characteristics in 76% of patients at any time point during the course of the disease. This relatively high CTC occurrence in BC should be considered when planning the long-term patient monitoring.
本研究分析了乳腺癌(BC)患者的外周血样本。通过基于大小的分离从外周血中富集循环肿瘤细胞(CTC),然后进行体外培养。本研究的主要目的是展示一种具有高 CTC 回收率的抗原非依赖性 CTC 分离方法。随后,对治疗过程中多次富集的 CTC 进行了分子特征分析。
纳入了不同分期的 BC 患者(N=167)进行研究。所有患者均为手术、手术诊断或化疗的候选者。同时,20 名患者定期接受监测,除了检测 CTC 的存在外,还通过 qPCR 检测 CTC 特征,特别关注 HER2 和 ESR 状态。
在该队列中,CTC 阳性率为 76%。在测试组之间没有显著差异,但在接受手术和新辅助治疗前开始治疗的组中,CTC 的发生率最高。另一方面,在绝经后患者组(56%)、ESR+患者组(60%)和 DCIS 组(44.4%)中,CTC 频率最低。值得注意的是,新辅助治疗(NACT)完成后,77.7%的病例中存在 CTC。另一方面,接受激素治疗的患者只有 52%的病例 CTC 阳性。
有趣的是,CTC 的 HER2 和 ESR 状态与原发性肿瘤的状态不同。在 50%的患者中,CTC 上的 HER2 状态不仅从 HER2+变为 HER2-,而且从 HER2-变为 HER2+(33%)。在 CTC 中,ESR 状态仅从 ESR+变为 ESR-。
本研究获得的数据表明,BC 是一种异质性疾病,但在疾病过程中的任何时间点,76%的患者都可以独立于疾病特征检测到 CTC。在计划对患者进行长期监测时,应考虑到 BC 中相对较高的 CTC 发生率。