Circulating tumor DNA (ctDNA) offers the possibility of accessing the tumor genome from circulating blood through a simple blood test. It is currently used for diagnostic, prognostic and predictive purposes of response or resistance to oncological treatments. These advances in ctDNA have been made possible by major developments in molecular biology techniques in recent years, as the detection of ctDNA requires very sensitive techniques such as Next Generation Sequencing (NGS). CtDNA overcomes this problem of very limiting tumor heterogeneity during a solid biopsy. All of these applications make circulating DNA an increasingly essential tool in the management of cancer patients. The studies are currently in most cases on small numbers and are retrospective. In addition, exosomes are also a biomarker of the future that can also be detected in the bloodstream . Exosomes are nanovesicles 50 to 200 nm in diameter released into the extracellular environment via the endosomal pathway by fusion with the plasma membrane. They are very informative since they transport tumor genetic material in the form of DNA, mRNA and miRNA, but also adhesion proteins, immunostimulatory molecules and cytoskeleton, enzymes and Heats shock proteins ( HSP). The aim of the ADIGYN study is to set up a large prospective cohort to assess the diagnostic, prognostic and predictive impact of ctDNA and exosomes in digestive and gynecological / breast cancers. From the circulating DNA, we characterize the ActDNA on the molecular level thanks to the study of different point mutations usually used but also of new described mutations having a therapeutic impact and the search for other genetic alterations having an impact on the therapeutic strategy (such as microsatellite instability) or the study of exosomes and their composition. To assess resistance to oncological treatments, ctDNA will be analyzed at the start of treatment, during treatment, during progression and / or relapse and also during monitoring or treatment break
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
1,000
Only blood samples at different times of treatment
CHU POitiers
Poitiers, France
RECRUITINGTo assess the prognostic impact of ctDNA (mortality) in digestive and gynecological / breast cancers.
Correlation between ctDNA and overall survival
Time frame: Through study completion, an average of 12 months
Evaluate the diagnostic value of ctDNA and exosomes
ct DNA and exosomes analyses can be new tools for cancer diagnosis
Time frame: Through study completion, an average of 12 months
Evaluate the prognostic impact of exosomes and their composition
There are many kind of exomossomes with few different composition and different roles
Time frame: Through study completion, an average of 12 months
Evaluate the predictive benefit of response / resistance to ctDNA and exosome treatments
Correkation between ctDNA/exosomes and progression free survival
Time frame: Through study completion, an average of 12 months
Evaluate the possibility of detecting certain molecular alterations using ctDNA and exosomes
With new technics of biology molecular, we are going to try to detect molecular alterations in ctDNA /exosomes
Time frame: Through study completion, an average of 12 months
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