Clinical Trials Directory

Trials / Completed

CompletedNCT02546453

Use of Specific Genetic Alteration s of Tumoral Cells Identified by the Next Generation Sequencing Techniques (NGS) to Follow Peripheral Samples of Children With Metastatic and/or High Risk Solid Tumor - NGSKids

Use of Specific Genetic Alteration s of Tumoral Cells Identified by NGS to Follow Peripheral Samples of Children With Metastatic and/or High Risk Solid Tumor -

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Institut Curie · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The search for genetic alterations in primary tumor by NGS techniques followed by the detection of these alterations in circulating tumor DNA and/or CTC/DTC present in peripheral samples (blood, cerebrospinal fluid, bone marrow, possibly urine) collected during several steps and after the treatment could be a tool to monitor the response during and after the treatment.

Conditions

Interventions

TypeNameDescription
BIOLOGICALTumoral specific genetic alterationsA buccal swab and a blood sample will be used at the diagnostic to identify the specific genetic alterations of tumoral cells.
BIOLOGICALTumoral specific genetic alterationsCollection of blood (maximum 9 samples of 3 to 5 ml), bone marrow (maximum 3 samples of 3 to 5 ml) and cerebral spinal fluid (maximum 3 samples 500µl to 1ml).

Timeline

Start date
2014-09-01
Primary completion
2021-01-01
Completion
2021-01-01
First posted
2015-09-10
Last updated
2024-01-31

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02546453. Inclusion in this directory is not an endorsement.