跳至主要内容
临床试验/NCT06478056
NCT06478056已完成不适用

Correlation of Portal and Peripheral Venous ctDNA in Pancreatic Adenocarcinoma

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年5月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
level of ctDNA

研究概览

简要总结

This study aims to evaluate the prognostic impact of the detection of circulating tumor DNA in peripheral venous blood, portal venous blood, collected intraoperatively, as well as its detection in peritoneal fluid.

详细描述

Pancreatic adenocarcinoma is the 6th most common cancer in France and is expected to be the 2nd leading cause of cancer mortality in Europe by 2030. Its overall 5-year survival for all stages combined is estimated at 7-8%.

Surgery is the only potentially curative treatment for pancreatic adenocarcinoma (PA), although only 10-20% of patients present with resectable disease. The oncological results of surgery alone are disappointing (median overall survival (OS) of 15-20 months and 5-year OS of 8-15%), due to the high frequency of recurrence. For this reason, surgery must be integrated into a comprehensive treatment sequence, also known as multimodal therapy.

Significant progress has been observed over the past 5 years, with a marked increase in median OS in recent clinical trials, and an intensification of perioperative chemotherapy (CT) protocols.

Liquid biopsy and circulating biomarkers show promise for improving the multidisciplinary approach to treatment of pancreatic adenocarcinoma.

Circulating tumor DNA (ctDNA) is the most extensively studied marker in blood liquid biopsies and can provide insight into the molecular profile and individual characteristics of the tumor. This could pave the way for the identification of new therapeutic targets and markers of tumor response to complement diagnosis and provide improved stratified treatment. Similarly, the measurement of tcDNA in peritoneal fluid could provide a better understanding of individual tumour characteristics and the risk of peritoneal metastasis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 18 years
  • •Patient with operable pancreatic adenocarcinoma (resectable or boderline with or without neoadjuvant therapy) with histological evidence or indirect diagnostic criteria (CA 19-9 Significant (≥ 200 U/ml), pancreatic hypodense lesion without differential diagnosis)
  • •Biological criteria: Neutrophils > 1,500 cmm, platelet count > 100,000 cmm, creatinine clearance (Cockroft and Gault equation) > 60 ml/min, hemoglobin > 10 g/dl.
  • •ECOG performance status 0 or 1
  • •Patient has read and understood the information letter and signed the non-opposition/consent form.
  • •For an adult unable to give consent: Representative of the adult who has read and understood the information letter and signed the consent form

排除标准

  • •Other active cancer or haematological malignancy
  • •Uncontrolled congestive heart failure - untreated angina pectoris; recent myocardial infarction (within the last year) - uncontrolled hypertension (SBP > 160 mm or DBP > 100 mm, despite optimal drug therapy), long QT.
  • •Uncontrolled major infections, chronic infectious diseases, immunodeficiency syndromes
  • •Premalignant hematological disorders, e.g. myelodysplastic syndrome
  • •Severe hepatic impairment
  • •Patients not registered with social security
  • •Pregnant, parturient or breast-feeding woman (a pregnancy test will be carried out unless there is a history of hysterectomy, tubal ligation or menopause)
  • •Person deprived of liberty by an administrative or judicial decision, or person placed under court protection, sub-guardianship or guardianship.
  • •History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol, or to prevent him/her from giving informed consent.
  • •Treatment contraindicated for venous sampling

研究组 & 干预措施

Surgery

Other

patients operated on for pancreatic adenocarcinoma in the digestive surgery department of Rouen University Hospital

干预措施: pancreatectomy (Procedure)

结局指标

主要结局

level of ctDNA

时间窗: Surgery

the level of ctDNA measured in peripheral venous and portal blood before and after mobilization of the specimen during surgery

次要结局

  • level of ctDNA(surgery)
  • peritoneal ctDNA level(surgery)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Correlation of Portal and Peripheral Venous ctDNA in... | 临床试验