Colorectal Neoplasms Clinical Trial
Official title:
Search for the Presence of Genetic Alteration in the Plasma of Patients With Stage II-III Colorectal Cancers: Prognosis Impact
Cancer is a DNA disease characterized by the presence of genetics alterations in cancer
cells.
The recent studies underline that these recurring alterations must be considered as a good
molecular marker. In fact, they could use for tumor DNA detection in different biological
fluids.
So, the main purpose is to define the presence of circulating tumor DNA in the patients
plasma with colorectal cancer, by the presence of mutation (KRAS, NRAS, BRAF, APC, TP53 and
MIRCOSATELLIE instability).
These molecular analysis will be done both in tumor and plasma samples,
This trial allows to characterize the prognostic value of circulating tumoral DNA presence in
colorectal cancer.
Two major issues appear in improving the prognosis of cancer patients, the first is early
detection and the second is the risk of recurrence or the early diagnosis of recurrence in
order to propose the most appropriate treatment for patients.
Cancer is a DNA disease that is characterized by the acquisition by the tumor cell during
carcinogenesis of a number of recurrent genetic alterations. The development of molecular
tools that can easily characterize these abnormalities specific to tumor cells, allows us to
consider their use in clinical practice. These genetic alterations could represent useful
molecular markers for detecting the presence of tumor DNA in various biological fluids
including plasma of cancer patients. This circulating tumor DNA, whose nature is confirmed by
the similarity of genetic alterations with those observed from DNA extracted from tumor cells
of the patients, represents a molecular marker of cancer available from a single sample and
could be an alternative to the use of more conventional markers such as CEA. We propose in
this study to confirm the predictive value on the risk of recurrence or metastasis of
circulating tumor DNA in plasma of patients with colorectal cancer from a cohort study (250
patients with non-metastatic colorectal cancer (Stage II and III). This is a multicenter
prospective study. The cohort of patients will be followed for a minimum period of 36 months.
A biological analysis of the tumor in search for the main genetic alterations of colorectal
cancer cells will be made (KRAS, NRAS, TP53, BRAF and APC mutations as well as the presence
of a microsatellite instability). These same genetic alterations will be sought on a plasma
sample taken before surgery and during follow-up (9 samples in total). The objectives of this
study will be 1/to assess the prognostic value of the presence of circulating tumor DNA in
plasma, by searching for an association between the risk of and the presence of genetic
alteration in the plasma of these patients, 2/to search for a relationship between initial
rate of circulating tumor DNA and the risk of local recurrence,3/ to characterize the
relationship between the type of alterations in the plasma at the initial diagnosis of
circulating tumor DNA and the risk of recurrence 4/ to assess during the follow-up the
prognostic value of the occurrence of tumor circulating DNA.
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