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临床试验/NCT06955767
NCT06955767尚未招募不适用

Performance of Serum Matrix Metalloproteinase (MMP14) Assay as a Novel Biomarker for Colorectal Cancer Screening in Subjects From 50 to 74 Years Old Referred for Colonoscopy After Positive FIT

CHU de Reims1 个研究点 分布在 1 个国家目标入组 650 人开始时间: 2025年5月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
CHU de Reims
入组人数
650
试验地点
1
主要终点
Serum Matrix Metalloproteinase (MMP14) : normal versus a cancerous lesion

研究概览

简要总结

Colorectal cancer is the third most common cancer in men, and the second most common in women. Screening for colorectal cancer is based on the search for blood in the stool using fecal immunochemical test (FIT). Occult bleeding is an indication for colonoscopy. In a FIT positive population, 60% of colonoscopies are negative, 34% diagnose an adenomatous lesion, and 6% a cancer. The identification of new biological markers could reduce the number of colonoscopies performed. Cancer cells release extracellular vesicles that contain proteins, mRNAs, DNA, which they can transfer to neighbouring or distant cells. The use of exosomal proteins as novel tumor markers looks very promising. We performed a pilot study comparing the levels of different exosomal proteins in 74 subjects which was recently accepted for publication in Journal of Clinical Laboratory Analysis. Comparison of results showed that only matrix metalloproteinase 14 (MMP14) was significantly higher in patients with colorectal cancer or adenoma than in people with normal colonoscopy.

The primary objective of the current study is to determine the best cut-off value of MMP-14 for colorectal cancer screening and to evaluate the performance (Sensitivity, Specificity...) associated to this cut-off value. The secondary objective will be to determine the best cut-off value of MMP-14 for colorectal adenomas screening and to evaluate its performance.

For this purpose, 650 patients, seen for diagnostic colonoscopy following a positive FIT test, will be included in the study. After blood collection and exosome isolation, MMP-14 will be measured using a quantitative test (enzyme-linked immunosorbent assay) and the results will be associated with colonoscopy results to determine the sensitivity, specificity, positive predictive value (PPV) and net present value (NPV).

详细描述

Inclusion criteria: Individuals presenting for colonoscopy with a positive FIT result.

  • Positive fecal immunoassay requiring total colonoscopy under general anesthesia.
  • Persons having agreed to participate in the study (signed consent form)
  • Adults affiliated to a health insurance scheme.

Non-inclusion criteria:

  • History of other cancer not in remission or in remission for less than five years (with the exception of cervical cancer or basal cell skin cancer treated with curative intent)
  • Patients undergoing chemotherapy
  • Patients protected by law This is a cross-sectional multicenter interventional study. Patients will be recruited from the Hepato-Gastroenterology departments of the CHU de Reims, CHU de Dijon, CHU de Nancy, CHU de Besançon, CH de Châlons-en-Champagne, Institut Jean Godinot de Reims, CHU de Strasbourg, CH de Charleville Mézières and CH d'Epernay.

Once consent has been signed and the patient has been included in the study, blood will be drawn from 2 additional tubes of 5 ml each, either in the consultation room or in the operating room, when the infusion is set up for colonoscopy under general anaesthetic. Plasma will be collected at the various participating facilities (2 x 5mL EDTA tubes), centrifuged at 1000g for 10 minutes, then frozen at -80°C. Samples will then be sent to the Reims University Hospital Biology Department for storage before analysis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
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

入选标准

  • Individuals presenting for colonoscopy with a positive FIT result.
  • Positive fecal immunoassay requiring total colonoscopy under general anesthesia.
  • Persons having agreed to participate in the study (signed consent form)
  • Adults affiliated to a health insurance scheme.

排除标准

  • History of other cancer not in remission or in remission for less than five years (with the exception of cervical cancer or basal cell skin cancer treated with curative intent)
  • Patients undergoing chemotherapy
  • Legally protected individuals

结局指标

主要结局

Serum Matrix Metalloproteinase (MMP14) : normal versus a cancerous lesion

时间窗: At 30 minutes

Concentration of Serum Matrix Metalloproteinase (MMP14) depending on whether the colonoscopy was normal or revealed a cancerous lesion

次要结局

  • Diagnostic performances of Serum MMP14(At 30 minutes)
  • Serum Matrix Metalloproteinase (MMP14) MMP14 Concentration: Normal vs. Adenoma(At 30 minutes)
  • Serum MMP14 Concentration according to adenoma characteristics(At 30 minutes)
  • Serum MMP14 Concentration between groups: normal colonoscopy vs. adenoma and cancerous lesions(At 30 minutes)
  • Concentration of markers derived from circulating tumor exosomes in the context of colorectal cancer(At 30 minutes)

研究者

发起方
CHU de Reims
申办方类型
Other
责任方
Sponsor

研究点 (1)

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