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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Tumoral specific genetic alterations | A buccal swab and a blood sample will be used at the diagnostic to identify the specific genetic alterations of tumoral cells. |
| BIOLOGICAL | Tumoral specific genetic alterations | Collection 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.