⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Diagnostic and Prognosis Value of Circulating DNA for CRC Patients' Surveillance After Curative Treatment

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Diagnostic and Prognosis Value of Circulating DNA for CRC Patients' Surveillance After Curative Treatment

Official Title: Diagnostic and Prognosis Value of Circulating DNA for CRC Patients' Surveillance After Curative Treatment

Study ID: NCT02813928

Interventions

ccfDNA analysis

Study Description

Brief Summary: Inspite of curative treatment 30-50% patients with ColoRectal Cancer (CRC) develop tumor relapse during the first 3 years after treatment of the primary tumor. Treatment of relapses is based on surgical resection, when possible, chemotherapy and targeted therapies. To detect recurrences or metastases, a surveillance strategy is recommended for patients able to withstand complementary treatment during a five-year period. Over this period, the probability of one false-positive result is 87%. Considering that less than 10% of recurrent patients are suitable for potentially curative treatment and that more intensive programs enable an increase of the overall rate of curative resection but do not result in reduced mortality, less time and cost-consuming, tailored follow-up is necessary. The level of circulating ccfDNA, defined as extra cellular DNA, increases in CRC patients. The Inplex® method could validate the use of ccfDNA as a cancer biomarker in terms of prognosis and surveillance. Tubes for ccfDNA analysis will be taken during medical examination at the same time of the CEA dosage (if it was not made before the consultation). Cryotubes of plasma will be sent for analysis in the laboratory INSERM (National Health Institute) of Montpellier and the remaining plasma will be kept in biological collection. Patients will have a consultation of follow-up every 3-4 months during which the dosage of CEA and ccfDNA will be realized as well as a medical examination, a general examination (weight, size, and blood pressure), an evaluation of the indices of performance status and a nutritional evaluation in case of loss of weight.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Aurillac Hospital, Aurillac, , France

Bergonie institute, Bordeaux, , France

Bordeaux University Hospital, Bordeaux, , France

Les Cèdres clinical, Brive-la-Gaillarde, , France

Brive Hospital, Brive, , France

Cahors Hospital, Cahors, , France

Clermont Ferrand University Hospital, Clermont-Ferrand, , France

Gueret Hospital, Guéret, , France

La marche clinical, Guéret, , France

Limoges Hospital, Limoges, , France

Montpellier Institute, Montpellier, , France

Montpellier University Hospital, Montpellier, , France

Moulins Hospital, Moulins, , France

Saint Antoine AP-HP, Paris, , France

Perigueux clinical, Périgueux, , France

Périgueux Hospital, Périgueux, , France

Saint Junien Hospital, Saint-Junien, , France

Sainte feyre Hospital, Sainte feyre, , France

Vichy Hospital, Vichy, , France

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: