Monitoring Circulating Tumor DNA and Evaluating Prognostic and Predictive Impact of Liquid Biopsy in Advanced HER2 Negative Gastric Cancer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Prognostic molecular markers.
研究概览
简要总结
This study aims to evaluate the use of next generation sequencing (NGS) to detect circulating tumor DNA in advanced HER2 negative gastric cancer patients. The evaluation of the therapy efficacy for gastric cancer patients is usually evaluated by computer tomography scans with RECIST criteria that are performed every two months during the treatment. In this study, we will compare the monitoring of circulating tumor DNA with the results of CT scan according the RECIST criteria and the blood level of CEA and CA 19-9 tumor markers.
详细描述
Gastric cancer is one of the common malignant tumors in China, with relatively high incident rate and mortality among the population. More than 80% of gastric cancer are in advanced stage.
Circulating tumor DNA (ctDNA) is tumor-derived fragmented DNA with an average size of 166 bp, mixed with cell free DNA (cfDNA) of other sources in blood circulation.ctDNA is reflecting the most up-to-date status of tumor genome. Hence, it is considered as a new biomarker for tumor, which can be qualitative, quantitative and used for disease monitoring. Detecting ctDNA, in most patients, allows for the noninvasive molecular characterization detection of tumors, including genetic changes that are revealed by the selective pressure of therapies. Considering the origin of ctDNA, it can be from different subclones of primary tumor or both primary and metastatic tumors, the ctDNA may overcome the problems caused by tumor heterogeneity. Additionally, the short half-life of ctDNA, about 2 hours, makes ctDNA an ideal dynamic marker of tumor bulk.
Molecular events including gene mutation, fusion and amplification will be detected by next generation sequencing platform using ctDNA collected from peripheral blood samples of gastric cancer patients. Samples will be collected at baseline, every two months in the surveillance after treatment and disease progression.
Thus, the objective of this study is to identify a prognostic and/or predictive biomarker of tumor response according to the tumor DNA circulating assessment in gastric cancer treatment, in order (i) to avoid an unnecessary toxicity of an ineffective treatment that it would be continued uselessly, (ii) and to allow a early changing to an alternative therapy regimen.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female patients age 18 -
- •Histologically confirmed adenocarcinoma of gastric or gastro-oesophageal junction. Gastric tumors should be treatment naïve unresectable or metastatic disease, or recurrence over 6 months after finish of adjuvant chemotherapy.
- •HER2 status is confirmed by IHC/FISH. HER2 negative: IHC 0/1+ or IHC 2+ plus FISH negative.
- •At least one measurable lesion should be confirmed by imaging examination.
- •Eastern Cooperative Oncology Group (ECOG) performance status 0 or
- •No concomitant other malignant tumor or treated malignant tumor within last five years.
- •Eligible peripheral blood and tissue samples.
- •Willing to provide clinicopathological information and imaging information.
排除标准
- •Patients received systemic treatment before enrolled or finished adjuvant chemotherapy less than 6 months.
- •With second primary malignant diseases.
- •HER2 status is confirmed by IHC/FISH. HER2 positive: IHC 3+ or IHC 2+ plus FISH positive.
- •No qualified paired tissue samples.
- •No complete clinicopathological information and follow-up.
- •Presence of any systemic illness incompatible with participation in the clinical trial or inability to provide written informed consent.
- •Other situations assessed by investigator can disturb quality control of the investigation.
结局指标
主要结局
Prognostic molecular markers.
时间窗: 2 years
Change from baseline in molecular biomarkers at time on disease progression
The sensitivity and specificity of ctDNA detection. Profiling of the most frequently detected gene mutations and level of mutations in ctDNA
时间窗: 2 years
次要结局
- Mechanisms of therapy resistance(2 years)
- Mutation profile and the concordance of mutations in tumor tissue and ctDNA of gastric cancer(2 years)
- The concordance and accuracy of response evaluation results determined by ctDNA compared with imaging and serum tumor biomarkers (CEA, CA19-9,CA72-4 et al).(2 years)
- Relative frequency of targetable mutations (incl. TMB and MSI status).(2 years)
研究者
chenwu
Department of Oncology
The First People's Hospital of Changzhou