Molecular Profiling to Improve Outcome of Patients in Cancer. A Pilot Study
NCT03546127 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24
Last updated 2025-09-11
Summary
Next Generation Sequencing in cancer: a feasibility study in France to assess sample circuit and to perform analyzes within a limited time.
Conditions
- Colorectal Carcinoma
- Soft Tissue Sarcoma
Interventions
- GENETIC
-
Next Generation Sequencing (NGS): exome, RNA seq
Tumor and blood samples will be sequenced at medium-high coverage at the whole genome (exome) and transcriptome levels (RNA Seq). This will allow detecting variants in a larger set of samples even though only from the main clone will be precisely measured. The whole exome will be performed at a mean coverage of at least 60x for the normal DNA samples and 120x for the tumor DNA samples. The transcriptome of the tumor will be performed at enough depth of coverage to detect gene fusions, transcriptome variants and measure the digital expression of already annotated isoforms. For both sequencing configurations: * Data from each cancer and normal genome will be analysed for the presence of somatic variants. * DNA and RNA sequencing results will be integrated. * Technical replication for the mutations / chromosome alterations / transcript fusions that most likely drive the tumour process will be performed via Target Resequencing of the genomic / coding regions of interest.
Sponsors & Collaborators
-
Institut Bergonié
collaborator OTHER -
Plateforme labellisée Inca - Institut Bergonié, Bordeaux
collaborator UNKNOWN -
Plateforme labellisée Inca - Hôpital Européen Georges Pompidou, Paris
collaborator UNKNOWN -
CNRGH, Evry
collaborator UNKNOWN -
EUCLID Clinical Trial Platform
collaborator OTHER -
Institut National de la Santé Et de la Recherche Médicale, France
lead OTHER_GOV
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-05-23
- Primary Completion
- 2017-09-21
- Completion
- 2017-09-21
Countries
- France
Study Locations
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